MAT

fc52_e01a

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA MAT

fc52_e97d

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms MAT

fc52_7111

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) MAT

fc52_b46c

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA MAT

fc52_c244

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms MAT

fc52_8312

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA MAT

fc52_a126

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated MAT

fc52_b2c1

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms MAT

fc52_71c2

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA MAT

fc52_2574

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA MAT

fc52_b197

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA MAT

fc52_d9e0

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA MAT

fc52_0c68

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different MAT

fc52_70b7

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different MAT

fc52_ebbd

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) MAT

fc52_510e

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA MAT

fc52_b2ea

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA MAT

fc52_dd05

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses MAT

fc52_8b29

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms MAT

fc52_2216

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA MAT

fc52_f24a

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas MAT

fc52_3dc0

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different MAT

fc52_043e

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied MAT

fc52_9484

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied MAT

fc52_dc6f

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different MAT

fc52_4953

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas MAT

fc52_51bb

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA MAT

fc52_7017

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas MAT

fc52_6a71

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses MAT

fc52_af6c

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different MAT

fc52_2082

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses MAT

fc52_e507

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses MAT

fc52_af0a

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated MAT

fc52_9415

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses MAT

fc52_8e47

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different MAT

fc52_b862

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated MAT

fc52_403e

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated MAT

fc52_9c56

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA MAT

fc52_94ed

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms MAT

fc52_3f4c

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated MAT

fc52_8c92

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms MAT

fc52_ebab

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA MAT

fc52_115a

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms MAT

fc52_1f51

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA MAT

fc52_e2a0

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA MAT

fc52_3d6d

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms MAT

fc52_954b

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms MAT

fc52_5cd0

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas MAT

fc52_63d0

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas MAT

fc52_f0db

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms MAT

fc52_8777

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples MAT

fc52_b116

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated MAT

fc52_ac46

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms MAT

fc52_b3e3

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses MAT

fc52_9331

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA MAT

fc52_61a1

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses MAT

fc52_bfd2

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied MAT

fc52_a9ea

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA MAT

fc52_9e3e

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different MAT

fc52_548a

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses MAT

fc52_136d

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms MAT

fc52_7706

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples MAT

fc52_3d28

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses MAT

fc52_6164

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied MAT

fc52_cf09

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA MAT

fc52_5727

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA MAT

fc52_43cd

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas MAT

fc52_91ec

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms MAT

fc52_4cb6

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples MAT

fc52_d22a

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA MAT

fc52_296e

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) MAT

fc52_e92b

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples MAT

fc52_1d93

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied MAT

fc52_aaca

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses MAT

fc52_92b3

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples MAT

fc52_2d95

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples MAT

fc52_1ea9

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA MAT

fc52_9848

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different MAT

fc52_5676

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA MAT

fc52_88d4

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA MAT

fc52_fb75

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated MAT

fc52_3867

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different MAT

fc52_817c

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA MAT

fc52_c64f

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different MAT

fc52_94b9

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA MAT

fc52_e4d6

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different MAT

fc52_b3e6

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples MAT

fc52_beea

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) MAT

fc52_1a83

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms MAT

fc52_862a

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms MAT

fc52_462f

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas MAT

fc52_9e00

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated MAT

fc52_16f4

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples MAT

fc52_85bd

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated MAT

fc52_e56a

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms MAT

fc52_4822

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA MAT

fc52_4155

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA MAT

fc52_f106

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas MAT

fc52_9377

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses MAT

fc52_ada1

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA MAT

fc52_d602

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA MAT

fc52_aea1

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA MAT

fc52_772c

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) MAT

fc52_aacf

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms MAT

fc52_9182

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA MAT

fc52_2221

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA MAT

fc52_cc94

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied MAT

fc52_25a7

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied MAT

fc52_03db

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated MAT

fc52_c6fc

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA MAT

fc52_4041

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples MAT

fc52_7962

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms MAT

fc52_9cc3

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses MAT

fc52_6d5f

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas MAT

fc52_8300

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA MAT

fc52_0964

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms MAT

fc52_c31f

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) MAT

fc52_a161

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms MAT

fc52_5ea3

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied MAT

fc52_ba2b

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated MAT

fc52_d7b6

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA MAT

fc52_95a8

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms MAT

fc52_261d

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA MAT

fc52_833e

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples MAT

fc52_a8a4

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA MAT

fc52_d7bc

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different MAT

fc52_c3ff

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C MAT

fc52_3c75

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated MAT

fc52_baf4

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) MAT

fc52_a8eb

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C MAT

fc52_e0a1

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses MAT

fc52_682b

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA MAT

fc52_ad6a

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) MAT

fc52_26e1

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas MAT

fc52_6f11

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C MAT

fc52_30ad

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas MAT

fc52_712a

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas MAT

fc52_f9a2

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA MAT

fc52_0c3a

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA MAT

fc52_e2f2

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA MAT

fc52_3a59

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different MAT

fc52_e79a

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples MAT

fc52_fcc1

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms MAT

fc52_d257

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated MAT

fc52_f4a1

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C MAT

fc52_2855

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA MAT

fc52_c85c

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) MAT

fc52_f49f

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different MAT

fc52_1bfa

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas MAT

fc52_7f55

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated MAT

fc52_f54f

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated MAT

fc52_d874

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses MAT

fc52_8cd3

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C MAT

fc52_9627

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different MAT

fc52_b3d3

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA MAT

fc52_4201

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated MAT

fc52_f56c

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated MAT

fc52_b89b

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms MAT

fc52_5d25

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses MAT

fc52_f0c7

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms MAT

fc52_1fbd

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) MAT

fc52_d23f

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms MAT

fc52_054a

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA MAT

fc52_cd44

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied MAT

fc52_c1f4

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different MAT

fc52_834d

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) MAT

fc52_d96e

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms MAT

fc52_97b1

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA MAT

fc52_b187

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied MAT

fc52_45b7

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different MAT

fc52_a279

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms MAT

fc52_1408

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas MAT

fc52_08ec

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA MAT

fc52_7416

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses MAT

fc52_0a67

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA MAT

fc52_1da4

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA MAT

fc52_ab57

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses MAT

fc52_174b

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA MAT

fc52_43c3

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated MAT

fc52_cc4c

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA MAT

fc52_d66d

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas MAT

fc52_8102

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C MAT

fc52_c363

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms MAT

fc52_9f34

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms MAT

fc52_a056

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied MAT

fc52_c040

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA MAT

fc52_a38e

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) substrate is enriched with a heavy isotopes to be consumed by the organisms to be studied BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) MAT

fc52_a20d

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms MAT

fc52_20ed

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C MAT

fc52_de83

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms MAT

fc52_29e5

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms MAT

fc52_08d8

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses MAT

fc52_7e08

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses stable isotope probing (SIP) relies on the consuption of a substrate that is highly enriched by an isotope, such as ¹³C suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA MAT

fc52_d0e3

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas MAT

fc52_7dda

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) environmental sample of 16S rRNA from bacteria is labeled with a carbon isotope (¹³C) BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples MAT

fc52_ef0a

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) identical mRNA is removed from two different samples leaving only mRNA that is different RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses MAT

fc52_c287

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

BrdU a labeled nucleotide is incorporated into the DNA of actively growing bacteria or viruses RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA MAT

fc52_3838

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

suppressive subtraction hybridization (SSH) takes advantage of the genetic differences between samples from two different areas BrdU bacteria that are actively growing will take up a nucleotide analog and incorporate it into its DNA RNA stable isotope probing (RNA-SIP) active labeled substrate metabolism and incorporation of heavier mass isotopes into the RNA stable isotope probing (SIP) adding heavy isotopes to an environmental sample to distinguish actively growing organisms MAT

fc52_5566

Match each of the following methods of culture enrichment with their corresponding descriptions.

Note: Each choice will be used exactly once.

RNA stable isotope probing (RNA-SIP) adding heavy isotopes into SSU ribosomal RNA to distinguish metabolically active organisms suppressive subtraction hybridization (SSH) compares microorganisms present in two different samples by removing identical DNA BrdU halogenated nucleotides that can be incorporated into newly synthesized DNA and isolated stable isotope probing (SIP) isotope-labeled carbon (¹³C) or nitrogen (¹⁵N) sources are assimilated into microbial environmental samples