Deck 18: Methods in Microbial Ecology
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ملء الشاشة (f)
Deck 18: Methods in Microbial Ecology
1
For microbial biodiversity studies,it is common to identify the ________ rather than the ________ as a measure of biodiversity.
A) organisms themselves / genes
B) genes / organisms themselves
C) cell types / genes
D) cell types / organisms themselves
A) organisms themselves / genes
B) genes / organisms themselves
C) cell types / genes
D) cell types / organisms themselves
B
2
Laser tweezers are used for
A) testing the purity of a culture.
B) isolating individual cells.
C) separating aerobes from anaerobes.
D) enhancing the growth of fastidious organisms.
A) testing the purity of a culture.
B) isolating individual cells.
C) separating aerobes from anaerobes.
D) enhancing the growth of fastidious organisms.
B
3
Winogradsky columns are used primarily for enrichment of
A) aerobic cultures, although occasionally anaerobes do appear.
B) anaerobic cultures, although occasionally aerobes do appear.
C) aerobes, anaerobes, and phototrophs.
D) phototrophs, although occasionally heterotrophs do appear.
A) aerobic cultures, although occasionally anaerobes do appear.
B) anaerobic cultures, although occasionally aerobes do appear.
C) aerobes, anaerobes, and phototrophs.
D) phototrophs, although occasionally heterotrophs do appear.
C
4
The methodology of microbial ecology includes
A) enrichment and isolation of specific microbes.
B) cell-staining methods.
C) gene, transcript, and protein characterization.
D) enrichment and isolation of specific microbes, cell-staining, and gene, transcript, and protein characterization.
A) enrichment and isolation of specific microbes.
B) cell-staining methods.
C) gene, transcript, and protein characterization.
D) enrichment and isolation of specific microbes, cell-staining, and gene, transcript, and protein characterization.
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5
When dealing with stable isotopes,enzymes tend to favor
A) the lighter isotope.
B) the heavier isotope.
C) the isotopes in about equal proportions.
D) either the lighter or the heavier isotope, depending on environmental conditions.
A) the lighter isotope.
B) the heavier isotope.
C) the isotopes in about equal proportions.
D) either the lighter or the heavier isotope, depending on environmental conditions.
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6
The science of microbial ecology deals with
A) how microbial communities interact with each other and their environment.
B) microbial activity and biodiversity.
C) microbial gene regulation mechanisms in response to environmental change.
D) how the activity and biodiversity of microbial communities affect microbial interactions with each other and the environment.
A) how microbial communities interact with each other and their environment.
B) microbial activity and biodiversity.
C) microbial gene regulation mechanisms in response to environmental change.
D) how the activity and biodiversity of microbial communities affect microbial interactions with each other and the environment.
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7
Which fluorescent molecule enables visualization of living microorganisms?
A) acridine orange
B) DAPI
C) GFP
D) SYBR® Green
A) acridine orange
B) DAPI
C) GFP
D) SYBR® Green
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8
Which of the following methods do NOT involve nucleic acid hybridization?
A) RACE-FISH
B) FISH-MAR
C) phylochips
D) T-RFLP
A) RACE-FISH
B) FISH-MAR
C) phylochips
D) T-RFLP
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9
Which approach would help to identify biologically produced sulfur in a sediment sample?
A) enrichment
B) isotopic fractionation
C) microautoradiography
D) microelectrodes
A) enrichment
B) isotopic fractionation
C) microautoradiography
D) microelectrodes
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10
Amplification of chromosomal DNA from a single-cell is accomplished by
A) randomly initiating DNA replication throughout the chromosome.
B) creating thousands of primers that will prime DNA replication throughout the chromosome.
C) creating complementary DNA from transcripts of a single-cell.
D) cloning fragments of the chromosome from the single-cell into a multi-copy plasmid.
A) randomly initiating DNA replication throughout the chromosome.
B) creating thousands of primers that will prime DNA replication throughout the chromosome.
C) creating complementary DNA from transcripts of a single-cell.
D) cloning fragments of the chromosome from the single-cell into a multi-copy plasmid.
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11
Which method requires the addition of at least one radioactive chemical?
A) CARD-FISH
B) MAR
C) NanoSIMS
D) SIP
A) CARD-FISH
B) MAR
C) NanoSIMS
D) SIP
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12
Well-designed microbial activity measurements can reveal ________ of major metabolic reactions in a habitat.
A) types
B) rates
C) both types and rates
D) either types or rates (but not both)
A) types
B) rates
C) both types and rates
D) either types or rates (but not both)
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13
The biggest limitation of traditional light microscopy and electron microscopy methods is that they are unable to reveal
A) absolute cell concentration.
B) cellular components of small microbes because of the limits of magnification.
C) genetic and functional diversity of microorganisms in the habitat under study.
D) physical microbial interactions as found in nature.
A) absolute cell concentration.
B) cellular components of small microbes because of the limits of magnification.
C) genetic and functional diversity of microorganisms in the habitat under study.
D) physical microbial interactions as found in nature.
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14
In an agar dilution tube,microbial colonies grow
A) at the bottom of the tube.
B) on the sides of the tube, although some may be at the surface.
C) embedded in the agar, rather than growing on the surface.
D) on the surface, but some creep down the sides away from the surface.
A) at the bottom of the tube.
B) on the sides of the tube, although some may be at the surface.
C) embedded in the agar, rather than growing on the surface.
D) on the surface, but some creep down the sides away from the surface.
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15
Staining methods are suitable for obtaining ________ information about the number of cells in natural samples.
A) qualitative
B) quantitative
C) both qualitative and quantitative
D) neither qualitative nor quantitative
A) qualitative
B) quantitative
C) both qualitative and quantitative
D) neither qualitative nor quantitative
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16
The term used when an organism is studied in its natural environment is
A) au naturale.
B) in vitro.
C) in situ.
D) in toto.
A) au naturale.
B) in vitro.
C) in situ.
D) in toto.
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17
The term axenic is used to describe a(n)
A) anaerobic culture.
B) anoxygenic culture.
C) nutritionally deficient culture.
D) pure culture.
A) anaerobic culture.
B) anoxygenic culture.
C) nutritionally deficient culture.
D) pure culture.
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18
Phylogenetic stains,such as those used in FISH,hybridize with
A) ribosomal RNA.
B) mitochondrial DNA.
C) nuclear DNA.
D) RNA polymerase.
A) ribosomal RNA.
B) mitochondrial DNA.
C) nuclear DNA.
D) RNA polymerase.
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19
What technique(s)can be used to characterize the phylogenetic composition of a microbial community without culturing any of the members?
A) green fluorescent protein tagging
B) stable isotope techniques
C) radioisotope experiments
D) fluorescent in situ hybridization
A) green fluorescent protein tagging
B) stable isotope techniques
C) radioisotope experiments
D) fluorescent in situ hybridization
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20
Radioisotopes are useful when
A) very high sensitivity is required.
B) turnover rates need to be determined.
C) the fate of portions of particular molecules need to be followed.
D) very high sensitivity is required, turnover rates need to be determined, and the fate of portions of particular molecules need to be followed.
A) very high sensitivity is required.
B) turnover rates need to be determined.
C) the fate of portions of particular molecules need to be followed.
D) very high sensitivity is required, turnover rates need to be determined, and the fate of portions of particular molecules need to be followed.
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21
Metatranscriptomics and metaproteomics are favored over metagenomics when ________ is of more interest than ________.
A) gene presence / phylogeny
B) phylogeny / gene presence
C) function or gene expression / gene presence
D) gene presence / function or gene expression
A) gene presence / phylogeny
B) phylogeny / gene presence
C) function or gene expression / gene presence
D) gene presence / function or gene expression
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22
What unit is isotopic fractionation reported as?
A) parts per billion
B) parts per million
C) parts per thousand
D) parts per trillion
A) parts per billion
B) parts per million
C) parts per thousand
D) parts per trillion
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23
How do viability stains usually distinguish between living cells and dead cells?
A) The chemical fluoresces only when bound to ribosomes that are actively synthesizing proteins.
B) The chemical stain is taken up by living cells and once metabolized becomes fluorescent.
C) The dye specifically targets intact cytoplasmic membranes.
D) The dye's fluorescence is quenched by dead cells.
A) The chemical fluoresces only when bound to ribosomes that are actively synthesizing proteins.
B) The chemical stain is taken up by living cells and once metabolized becomes fluorescent.
C) The dye specifically targets intact cytoplasmic membranes.
D) The dye's fluorescence is quenched by dead cells.
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24
Thirty organisms containing the same phylogenetic marker are all considered to be within the same
A) phylotype.
B) species.
C) functional group.
D) phylogenetic tree.
A) phylotype.
B) species.
C) functional group.
D) phylogenetic tree.
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25
Analyses of sulfur isotopes have been used as evidence against life on the Moon,because the sulfides in lunar rocks have
A) an isotope composition similar to marine sulfate, which is enriched in ³⁴S.
B) an isotope composition similar to marine mud, which is depleted in ³⁴S.
C) an isotope composition similar to igneous rocks.
D) exactly equal amounts of ³⁴S and ³²S.
A) an isotope composition similar to marine sulfate, which is enriched in ³⁴S.
B) an isotope composition similar to marine mud, which is depleted in ³⁴S.
C) an isotope composition similar to igneous rocks.
D) exactly equal amounts of ³⁴S and ³²S.
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26
Interpreting stable isotopic fractionation depends on the fact that most enzymes preferentially bind ________ isotope substrates over ________ isotope substrates.
A) nonradioactive / radioactive
B) light / heavy
C) heavy / light
D) radioactive / nonradioactive
A) nonradioactive / radioactive
B) light / heavy
C) heavy / light
D) radioactive / nonradioactive
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27
Which of the following techniques can link prokaryotic phylogeny and function?
A) DAPI staining
B) stable isotope probing
C) environmental genomics
D) environmental genomics and stable isotope probing
A) DAPI staining
B) stable isotope probing
C) environmental genomics
D) environmental genomics and stable isotope probing
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28
In microbial ecology studies,the FISH technique identifies organisms based on
A) the presence of green fluorescent protein.
B) fluorescence of unique cofactors or pigments under certain wavelengths of UV light.
C) hybridization of a fluorescent probe to specific ribosomal RNA sequences.
D) the presence of luciferase.
A) the presence of green fluorescent protein.
B) fluorescence of unique cofactors or pigments under certain wavelengths of UV light.
C) hybridization of a fluorescent probe to specific ribosomal RNA sequences.
D) the presence of luciferase.
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29
Genes encoding ________ are widely used as target genes in molecular biodiversity studies.
A) ATPases
B) DNA polymerase III
C) 16S rRNA
D) RNA polymerase
A) ATPases
B) DNA polymerase III
C) 16S rRNA
D) RNA polymerase
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30
Robotic systems used to quickly test thousands of combinations of nutrients for enrichment of a particular prokaryotic species is an example of a(n)________ technology.
A) outdated
B) biased
C) genomic
D) high-throughput
A) outdated
B) biased
C) genomic
D) high-throughput
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31
When laser tweezers are used,the laser beam traps
A) isolated single-copy genomes.
B) a single microbial cell.
C) a single microbial colony on a plate.
D) multiple cells of the same type.
A) isolated single-copy genomes.
B) a single microbial cell.
C) a single microbial colony on a plate.
D) multiple cells of the same type.
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32
The rolled tube method is most commonly used for isolating which grouping of microorganisms?
A) anaerobes
B) chemolithotrophs
C) chemoorganotrophs
D) aerobes
A) anaerobes
B) chemolithotrophs
C) chemoorganotrophs
D) aerobes
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33
Diversity is often ________ when ARISA or T-RFLP is used.
A) underestimated
B) overestimated
C) not represented
D) biased
A) underestimated
B) overestimated
C) not represented
D) biased
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34
Collective estimates of the physiological reactions occurring in the entire microbial community are known as ________ measurements.
A) in vitro
B) in situ
C) activity
D) metagenomics
A) in vitro
B) in situ
C) activity
D) metagenomics
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35
For what purpose would a microbial ecologist use a microsensor?
A) to determine the concentration of cells in small increments in a sediment or water column
B) to determine the expression of a particular gene in a microbial community
C) to quantify the uptake of a radioactive material
D) to determine the concentration of O₂, N₂O, or other chemical species in small increments in a sediment or water column
A) to determine the concentration of cells in small increments in a sediment or water column
B) to determine the expression of a particular gene in a microbial community
C) to quantify the uptake of a radioactive material
D) to determine the concentration of O₂, N₂O, or other chemical species in small increments in a sediment or water column
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36
Why is it necessary to have a standard for the interpretation of stable isotope ratios?
A) A standard is necessary to calculate how much radioactivity was added to a sample.
B) A standard is necessary to determine the stable isotope ratio in the absence of biological activity.
C) A standard is necessary to determine the weight of each isotopes.
D) A standard is necessary to determine the age of the sample.
A) A standard is necessary to calculate how much radioactivity was added to a sample.
B) A standard is necessary to determine the stable isotope ratio in the absence of biological activity.
C) A standard is necessary to determine the weight of each isotopes.
D) A standard is necessary to determine the age of the sample.
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37
Which technique would be used to estimate the concentration of naturally occurring Escherichia coli in a wastewater sample?
A) agar dilution tube method
B) laser tweezers method
C) most probable number (MPN) method
D) cell tagging using GFP method
A) agar dilution tube method
B) laser tweezers method
C) most probable number (MPN) method
D) cell tagging using GFP method
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38
Microarrays are useful for assessing
A) gene expression.
B) enzyme activity.
C) the presence of specific rRNA sequences.
D) gene expression and the presence of specific rRNA sequences.
A) gene expression.
B) enzyme activity.
C) the presence of specific rRNA sequences.
D) gene expression and the presence of specific rRNA sequences.
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39
Which molecular method allows for the detection of a specific organism within a diverse microbial community?
A) fluorescent DNA staining using DAPI
B) viability staining
C) enrichment techniques
D) fluorescent in situ hybridization
A) fluorescent DNA staining using DAPI
B) viability staining
C) enrichment techniques
D) fluorescent in situ hybridization
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40
Genomic analysis of Prochlorococcus has revealed
A) the presence of bacteriorhodopsin.
B) variations in ribosomal genes within the same phylotype.
C) complete congruence of genes and genome structure within the same phylotype.
D) variation in functional genes within phylotypes, but high levels of gene conservation between cultured representatives and environmental populations.
A) the presence of bacteriorhodopsin.
B) variations in ribosomal genes within the same phylotype.
C) complete congruence of genes and genome structure within the same phylotype.
D) variation in functional genes within phylotypes, but high levels of gene conservation between cultured representatives and environmental populations.
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41
If properly constructed,a Winogradsky column can be used to isolate pure cultures.
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42
Strict anaerobic organisms are not suited for GFP reporters due to the protein requiring oxygen to fluoresce.
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43
How would you label and separate the DNA of unknown methylotrophs in a sample?
A) Incubate the sample with ¹³C-methane.
B) Hybridize the DNA to FISH probes.
C) Use DGGE to separate the strands of DNA in the sample.
D) Use T-RFLP to identify the methylotroph DNA in the sample.
A) Incubate the sample with ¹³C-methane.
B) Hybridize the DNA to FISH probes.
C) Use DGGE to separate the strands of DNA in the sample.
D) Use T-RFLP to identify the methylotroph DNA in the sample.
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44
The goal of environmental genomics is to detect as many genes as possible and then,if possible,to determine to the phylogeny of the organisms to which the genes belong.
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45
Which of the following hypotheses could be tested using microautoradiography fluorescence in situ hybridization (MAR-FISH)?
A) Bacteriorodopsin uses light energy to translocate protons.
B) Archaea are the main autotrophs in marine water samples taken 300m below the surface of the ocean.
C) The microbial community of agricultural soils is more phylogenetically diverse than the microbial community of native prairie soils.
D) The ammonia monooxygenase gene is present in members of the phylum Verrucomicrobium.
A) Bacteriorodopsin uses light energy to translocate protons.
B) Archaea are the main autotrophs in marine water samples taken 300m below the surface of the ocean.
C) The microbial community of agricultural soils is more phylogenetically diverse than the microbial community of native prairie soils.
D) The ammonia monooxygenase gene is present in members of the phylum Verrucomicrobium.
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46
Organisms in natural environments can be detected by assaying for the presence of their genes.
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47
Once a putative pure culture has been obtained from the environment,it is no longer necessary to check its purity.
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48
Single-cell genomics may help us
A) predict which microbes will be abundant based on the environmental conditions.
B) understand the physiology of uncultured microbes.
C) develop better enrichment culture methods.
D) understand the physiology of uncultured microbes and develop better enrichment culture methods.
A) predict which microbes will be abundant based on the environmental conditions.
B) understand the physiology of uncultured microbes.
C) develop better enrichment culture methods.
D) understand the physiology of uncultured microbes and develop better enrichment culture methods.
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49
Traditional enrichment culturing circumvents issues associated with "weed" species from overcoming the population.
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50
The ¹³C/¹²C isotopic ratio of geological rocks of different ages has been used as evidence for or against past biological activity,because compounds of biological origin
A) do NOT contain ¹³C.
B) have a higher proportion of ¹³C that compounds of geological origin.
C) have a lower proportion of ¹³C that compounds of geological origin.
D) are not well preserved in geological samples.
A) do NOT contain ¹³C.
B) have a higher proportion of ¹³C that compounds of geological origin.
C) have a lower proportion of ¹³C that compounds of geological origin.
D) are not well preserved in geological samples.
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51
The element(s)that have proven useful for stable isotope studies are
A) carbon.
B) nitrogen.
C) sulfur.
D) carbon, nitrogen, and sulfur.
A) carbon.
B) nitrogen.
C) sulfur.
D) carbon, nitrogen, and sulfur.
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52
Stable isotope probing (SIP)is a method that
A) causes cells that hybridize with a fluorescent probe to fluoresce under UV light.
B) compares the isotopic ratios of different compounds in the environment to determine whether they are of biological or geological origin.
C) uses substrates containing heavy isotopes to label the DNA of organisms that use those substrates.
D) compares the transcription of specific isotope labeled genes under different conditions.
A) causes cells that hybridize with a fluorescent probe to fluoresce under UV light.
B) compares the isotopic ratios of different compounds in the environment to determine whether they are of biological or geological origin.
C) uses substrates containing heavy isotopes to label the DNA of organisms that use those substrates.
D) compares the transcription of specific isotope labeled genes under different conditions.
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53
Which of the following statements is FALSE concerning enrichment bias?
A) Dilution of the inoculum may help to avoid enrichment bias in some cases.
B) Enrichment bias is impossible to overcome in some oligotrophic environments.
C) Enrichment bias resulted in the underestimation of prokaryotic diversity.
D) Enrichment bias favors organisms that grow quickly.
A) Dilution of the inoculum may help to avoid enrichment bias in some cases.
B) Enrichment bias is impossible to overcome in some oligotrophic environments.
C) Enrichment bias resulted in the underestimation of prokaryotic diversity.
D) Enrichment bias favors organisms that grow quickly.
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54
Transcription of various genes under particular environmental conditions can be studied by
A) CARD-FISH.
B) using a reporter gene that encodes for green fluorescent protein (GFP).
C) T-RFLP.
D) using a reporter gene that encodes for green fluorescent protein (GFP) or CARD-FISH.
A) CARD-FISH.
B) using a reporter gene that encodes for green fluorescent protein (GFP).
C) T-RFLP.
D) using a reporter gene that encodes for green fluorescent protein (GFP) or CARD-FISH.
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55
The purpose of the enrichment culture technique is to enrich for organisms with specific physiological properties from a microbial community.
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56
One way to study a microbial ecosystem is to isolate microorganisms from it and study their properties in laboratory culture.
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57
The overall purpose of DGGE is to
A) separate genomes that are less than 95% similar.
B) measure activity of cells that use DGGE as an energy source.
C) detect cells that utilize a specific radiolabeled substrate.
D) separate genes of the same length that differ in their denaturing profile due to sequence variation.
A) separate genomes that are less than 95% similar.
B) measure activity of cells that use DGGE as an energy source.
C) detect cells that utilize a specific radiolabeled substrate.
D) separate genes of the same length that differ in their denaturing profile due to sequence variation.
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58
Culture-independent approaches avoid issues associated with
A) detecting very rare phylotypes.
B) conflating phylogenetic and functional diversity.
C) growing organisms in the lab.
D) next generation sequencing.
A) detecting very rare phylotypes.
B) conflating phylogenetic and functional diversity.
C) growing organisms in the lab.
D) next generation sequencing.
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59
Enrichment cultures can be established by placing the inoculum into selective media and incubating under specific conditions.
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60
You would like to test the hypothesis that ammonia-oxidizing Archaea are more active and abundant than ammonia-oxidizing Bacteria in coastal marine water.What technique(s)or experiment(s)could you use to test this hypothesis?
A) environmental proteomics
B) fluorescent in situ hybridization (FISH)
C) stable isotope probing using ¹⁵N labeled ammonia
D) stable isotope ratios of ammonia and nitrite
A) environmental proteomics
B) fluorescent in situ hybridization (FISH)
C) stable isotope probing using ¹⁵N labeled ammonia
D) stable isotope ratios of ammonia and nitrite
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61
What are the pros and cons of traditional enrichment culture techniques? What advances in the last decade are improving enrichment culture techniques to aid the cultivation of uncultured microorganisms?
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62
Metaproteomics is a more developed field than metatranscriptomics due to the high sensitivity of mass spectrometry.
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63
What prior knowledge is required to use a phylochip to study the abundance of the different microbes present within a microbial community? How does this cause bias when using a phylochip to analyze microbial community structure?
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64
The Winogradsky column is a method for assessing the entire gene complement of a habitat,revealing both the biodiversity and metabolic capabilities of the microbial community at the same time.
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65
We know that that there are over 50 major phyla in Bacteria; however,only about 25 of these phyla have cultured representatives.Why is this? How are scientists attempting to culture representative from the 25 phyla that do not currently have any organisms in culture?
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66
Describe what an ITS region is in the context of prokaryotes,and explain the significance of the ITS region for microbial ecology.
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67
FISH technology can employ only a single phylogenetic probe.
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68
Phototrophic organisms in SIP experiments are often observed releasing ¹⁴CO₂ as measuring activity.
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69
By using simple microscopy techniques,it is possible to determine if a culture is contaminated with another organism.
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70
Describe how FISH can be used to determine which cells within a microbial community are actively degrading toluene.Assume the genes involved in the metabolic pathway have been sequenced from several microorganisms and vary only slightly from one another.
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71
The MPN technique is rarely applied in the food industry because any microbial presence in food is unsafe.
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72
Propose an experiment to identify members capable of assimilating monomers of lignin within a microbial community.
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73
A study of the human gut performed in 1982 used various types of plates under different growth conditions to describe and enumerate the microbes in the human gut.They concluded that the majority of the microbes in the human gut are Gammaproteobacteria.A study conducted in 2010 using next-generation sequencing to characterize 16S rRNA sequences concluded that the majority of the microbes in the human gut are Firmicutes and Bacteriodetes.Why did these studies have different conclusions? Which study do you think is most accurate?
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74
Combined with autofluoresence or fluorescent DNA probes,flow cytometry can separate or count populations of cells from aquatic environments.
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75
The diversity of microorganisms in culture collections is representative of the diversity of microorganisms found in nature.
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76
DGGE and T-RFLP are both molecular microbial ecology methods that use the polymerase chain reaction to amplify specific genes to assess diversity.
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77
In natural samples it is often difficult to differentiate live cells from dead cells or cells from nonliving matter.
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78
How can NanoSIMS be used to determine which Roseobacters most strongly use DMSP as a sulfur source within a coastal marine environment? Explain the NanoSIMS methodology in your answer.
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79
Several fluorogenic dyes can be used simultaneously in a sample as long as they each emit light at a different measurable wavelength.
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80
Using specific examples,when is it appropriate to use CARD-FISH rather than the traditional FISH method and vice-versa?
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