Microbiology Exam 2 (cont.) Flashcards

1
Q

A base substitution mutation in a gene sometimes does not result in a different protein. Which of the following factors could account for this?

a. the mutation affects only the sequence of amino acids, so the protein stays the same
b. the fact that such mutations are usually accompanied by a complementary deletion
c. the rarity of such mutations
d. some amino acids are produced from more than one codon
e. a correcting mechanism that is part of the mRNA molecule

A

d. some amino acids are produced from more than one codon

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2
Q
The following steps must be performed to make a bacterium produce human protein X: 
1-Translation; 2-Restriction enzyme; 3-Prokaryotic transcription; 4-DNA ligase; 5-Transformation; 6-Eukaryotic transcription; 7-Reverse transcription. 
Put the steps in the correct sequence.
A) 5, 2, 3, 4, 7, 6, 1
B) 1, 2, 3, 5, 4, 7, 6
C) 6, 7, 2, 3, 4, 5, 1
D) 6, 7, 2, 4, 5, 3, 1
E) 6, 2, 1, 3, 4, 5, 7
A

D) 6, 7, 2, 4, 5, 3, 1

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3
Q

A source of heat-stable DNA polymerase is

A) Agrobacterium tumefaciens.
B) Thermus aquaticus.
C) Saccharomyces cerevisiae.
D) Bacillus thuringiensis.
E) Pseudomonas.
A

B) Thermus aquaticus.

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4
Q

You have a small gene that you wish replicated by PCR. You add radioactively labeled nucleotides to the PCR thermocycler. After 3 replication cycles, what percentage of the DNA single strands are radioactively labeled?

A) 0%
B) 12.5%
C) 50%
D) 87.5%
E) 100%
A

D) 87.5%

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5
Q

A population of cells carrying a desired plasmid is called a

A) Library.
B) Clone.
C) Vector.
D) Southern blot.
E) PCR.
A

B) Clone.

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6
Q

If you have inserted a gene in the Ti plasmid, the next step in genetic engineering is
A) Transformation of E. coli with Ti plasmid.
B) Splicing T DNA into a plasmid.
C) Transformation of an animal cell.
D) Inserting the Ti plasmid into Agrobacterium.
E) Inserting the Ti plasmid into a plant cell.

A

D) Inserting the Ti plasmid into Agrobacterium.

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7
Q
A source of heat-stable DNA polymerase is
A) Agrobacterium tumefaciens.
B) Thermus aquaticus.
C) Saccharomyces cerevisiae.
D) Bacillus thuringiensis.
E) Pseudomonas.
A

B) Thermus aquaticus.

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8
Q
Pieces of DNA stored in yeast cells are called a
A) Library.
B) Clone.
C) Vector.
D) Southern blot
A

A) Library.

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9
Q
Which of the following is an advantage of using E. coli to make a human gene product?
A) Endotoxin may be in the product.
B) It doesn't secrete most proteins.
C) Its genes are well known.
D) It can't process introns.
A

C) Its genes are well known.

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10
Q

Subunit vaccines can be made by genetic modification of yeast cells. A side effect of these vaccines might be
A) The disease.
B) A yeast infection.
C) Due to extraneous material.
D) Failure of the vaccine to provide immunity.
E) None of the above.

A

E) None of the above.

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11
Q
In Figure 9.4, the vector is
A) A virus.
B) A plasmid.
C) A library.
D) RNA.
E) Pseudomonas.
A

B) A plasmid.

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12
Q
In Figure 9.4, the process required in step 5 is
A) Transformation.
B) Southern blotting.
C) PCR.
D) Transcription.
E) Conjugation.
A

A) Transformation.

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13
Q
In Figure 9.4, the resulting organism (a) is
A) Bacillus thuringiensis.
B) Pseudomonas fluorescens.
C) A tomato plant.
D) E. coli.
E) a plant × Pseudomonas hybrid.
A

C) A tomato plant.

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14
Q
Which of the following methods of making rDNA could be described as "hit or miss"?
A) Protoplast fusion
B) Viral transduction
C) Transformation
D) Cloning
E) Gene gun
A

A) Protoplast fusion

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15
Q
You want to determine whether a person has a certain mutant gene. The process involves using a primer and Taq. This process is 
A) Translation.
B) Restriction mapping.
C) Transformation.
D) PCR.
E) Site-directed mutagenesis.
A

D) PCR.

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16
Q
PCR can be used to identify an unknown bacterium because
A) The RNA primer is specific.
B) DNA polymerase will replicate DNA.
C) DNA can be electrophoresed.
D) All cells have DNA.
E) All cells have RNA.
A

A) The RNA primer is specific.

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17
Q
The figure at the left in Figure 9.3 shows a gene identified by Southern blotting. What will a Southern blot of the same gene look like after PCR?
A) a
B) b
C) c
D) d
E) e
A

D) d

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18
Q

If you have inserted a gene in the Ti plasmid, the next step in genetic engineering is
A) Transformation of E. coli with Ti plasmid.
B) Splicing T DNA into a plasmid.
C) Transformation of an animal cell.
D) Inserting the Ti plasmid into Agrobacterium.
E) Inserting the Ti plasmid into a plant cell.

A

D) Inserting the Ti plasmid into Agrobacterium.

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19
Q
A specific gene can be inserted into a cell by all of the following EXCEPT
A) Protoplast fusion.
B) A gene gun.
C) Microinjection.
D) Electroporation.
E) Agrobacterium.
A

A) Protoplast fusion.

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20
Q
In Figure 9.4, the vector is
A) A virus.
B) A plasmid.
C) A library.
D) RNA.
E) Pseudomonas.
A

B) A plasmid.

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21
Q
A population of cells carrying a desired plasmid is called a
A) Library.
B) Clone.
C) Vector.
D) Southern blot.
E) PCR.
A

B) Clone.

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22
Q
How many pieces will EcoRI produce from the plasmid shown in Figure 9.1?
A) 1
B) 2
C) 3
D) 4
E) 5
A

b. 2

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23
Q
In Figure 9.1, after digestion with the appropriate restriction enzyme, what is the smallest piece containing the ampicillin-resistance (amp) gene?
A) 0.17 kilobase pairs
B) 0.25 kbp
C) 1.08 kbp
D) 1.50 kbp
E) 3.00 kbp
A

D) 1.50 kbp

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24
Q
In Figure 9.2, the enzyme in step 1 is
A) DNA polymerase.
B) DNA ligase.
C) RNA polymerase.
D) Reverse transcriptase.
E) Spliceosome.
A

C) RNA polymerase.

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25
Q
In Figure 9.2, the enzyme in step 2 is
A) DNA polymerase.
B) DNA ligase.
C) RNA polymerase.
D) Reverse transcriptase.
E) Spliceosome.
A

D) Reverse transcriptase.

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26
Q
Which of the following is NOT an agricultural product made by DNA techniques?
A) Frost retardant
B) Bacillus thuringiensis insecticide
C) Nitrogenase (nitrogen fixation)
D) Glyphosate-resistant crops
E) Pectinase
A

E) Pectinase

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27
Q
Suicide genes can be controlled by the fimbriae-gene operator. This would result in the death of 
A) All cells.
B) Cells making flagella.
C) Cells making fimbriae.
D) Cells at 37°C.
E) Conjugating cells.
A

C) Cells making fimbriae.

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28
Q

E. coli makes insulin because
A) It needs to regulate its cell-glucose level.
B) It’s an ancient gene that now has no function.
C) The insulin gene was inserted into it.
D) It picked up the insulin gene from another cell.
E) No reason; it doesn’t make insulin.

A

C) The insulin gene was inserted into it.

29
Q
The value of cDNA in recombinant DNA is that
A) It lacks exons.
B) It lacks introns.
C) It's really RNA.
D) It contains introns and exons.
A

B) It lacks introns.

30
Q
Which enzyme does NOT make sticky ends?
A) Enzyme Recognition
BamHI G↓GATCC
CCTAG↑G
B) Enzyme Recognition
EcoRI G↓AATTC
CTTAA↑G
C) Enzyme Recognition
HaeIII GG↓CC
CC↑GG
D) Enzyme Recognition
HindIII A↓AGCTT
TTCGA↑A
E) Enzyme Recognition
PstI CTGC↓G
G↑ACGTC
A

C) Enzyme Recognition
HaeIII GG↓CC
CC↑GG

31
Q
Self-replicating DNA used to transmit a gene from one organism to another is a
A) Library.
B) Clone.
C) Vector.
D) Southern blot.
E) PCR.
A

C) Vector.

32
Q

The purpose of the Human Genome Project was to
A) Identify all of the human genes.
B) Sequence the nucleotides in human DNA.
C) Translate human DNA.
D) Identify genes of all organisms.
E) None of the above.

A

B) Sequence the nucleotides in human DNA.

33
Q

A colleague has used computer modeling to design an improved enzyme. To produce this enzyme, the next step is to
A) Look for a bacterium that makes the improved enzyme.
B) Mutate bacteria until one makes the improved enzyme.
C) Determine the nucleotide sequence for the improved enzyme.
D) Synthesize the gene for the improved enzyme.
E) Use siRNA to produce the enzyme.

A

C) Determine the nucleotide sequence for the improved enzyme.

34
Q
In Figure 9.4, the resulting P. fluorescens has
A) A tomato gene.
B) An E. coli gene.
C) A Bacillus gene.
D) A tomato and a Bacillus gene.
E) No new gene.
A

C) A Bacillus gene.

35
Q
In Figure 9.4, the purpose of this experiment is to
A) Put a gene into a plant.
B) Put an insecticide on plant leaves.
C) Put a gene in Bacillus.
D) Isolate Pseudomonas from a plant.
E) Make a better tomato.
A

B) Put an insecticide on plant leaves.

36
Q

The Pap test for cervical cancer involves microscopic examination of cervical cells for cancerous cells. A new, rapid diagnostic test to detect human papilloma virus (HPV) DNA before cancer develops is done without microscopic exam. The steps involved in this FastHPV test are listed. What is the second step?
A) Add an RNA probe for HPV DNA
B) Lyse human cells
C) Add enzyme-linked antibodies against DNA-RNA
D) Add enzyme substrate
E) It doesn’t matter.

A

A) Add an RNA probe for HPV DNA

37
Q
Gene silencing blocks an undesirable product by
A) Allosteric inhibition of an enzyme.
B) End-product repression.
C) Making double-stranded RNA.
D) Blocking transcription.
E) Blocking DNA replication.
A

C) Making double-stranded RNA.

38
Q
34) To see the results of your work in question 33, you need to use 
A) Northern blotting.
B) Southern blotting.
C) Western blotting.
D) Colony blotting.
E) Selection.
A

B) Southern blotting.

39
Q
35) Assume you have discovered a cell that produces a lipase that works in cold water for a laundry additive. You can increase the efficiency of this enzyme by changing one amino acid. This is done by 
A) Irradiating the cells.
B) Site-directed mutagenesis.
C) Enrichment.
D) Selective breeding.
E) Selection.
A

B) Site-directed mutagenesis.

40
Q

36) The use of an antibiotic-resistance gene on a plasmid used in genetic engineering makes
A) Replica plating possible.
B) Direct selection possible.
C) The recombinant cell dangerous.
D) The recombinant cell unable to survive.
E) All of the above.

A

B) Direct selection possible.

41
Q

Large numbers of bacterial cells are NOT found in crown galls because
A) The plant kills the bacteria.
B) Cell walls protect the plant from bacterial invasion.
C) A gene in plant cells is controlling growth.
D) Bacteria kill plants.
E) The assumption is not true; many bacteria are in the galls.

A

B) Cell walls protect the plant from bacterial invasion.

42
Q
PCR can be used to amplify DNA in a clinical sample. The following steps are used in PCR. What is the fourth step?
A) Collect DNA.
B) Incubate at 94°C.
C) Incubate at 60°C.
D) Incubate at 72°C.
E) Add DNA polymerase.
A

C) Incubate at 60°C.

43
Q

Which of the following processes CANNOT be used to insert foreign DNA into cells?
A) Transformation
B) Electroporation
C) Protoplast fusion
D) A gene gun
E) All of the above can be used to insert foreign DNA into cells.

A

E) All of the above can be used to insert foreign DNA into cells.

44
Q

The reaction catalyzed by reverse transcriptase is _____________.

a) mRNA –> protein
b) DNA –> DNA
c) DNA –> mRNA
d) tRNA –> mRNA
e) mRNA –> cDNA

A

e) mRNA –> cDNA

45
Q

Which of following is NOT an agricultural product made by DNA techniques?

a) glyphosate-resistant crops
b) Bacillus thuringiensis insecticide
c) nitrogenase (nitrogen fixation)
d) pectinase
e) frost retardant

A

d) pectinase

46
Q

Biotechnology involves the

a) use of microorganisms to make desired products.
b) use of animal cells to make vaccines.
c) development of disease-resistant crop plants.
d) use of microorganisms to make desired products and the use of animal cells to make vaccines.
e) use of microorganisms to make desired products, the use of animal cells to make vaccines, and the development of disease-resistant crop plants.

A

e) use of microorganisms to make desired products, the use of animal cells to make vaccines, and the development of disease-resistant crop plants.

47
Q

Which of the following is NOT a desired characteristic of DNA vectors used in gene cloning procedures?

a) self-replication
b) circular form of DNA or integrates into the host chromosome
c) large size
d) may replicate in several species
e) has a selectable marker

A

c) large size

48
Q

An advantage of synthetic DNA over genomic or cDNA is the ability to

a) obtain genes that lack introns.
b) insert desired restriction sites into the DNA sequence.
c) isolate unknown genes.
d) make DNA from cellular RNA and the enzyme reverse transcriptase.
e) obtain genes that lack exons.

A

b) insert desired restriction sites into the DNA sequence.

49
Q

An advantage of cDNA over genomic DNA is that it

a) lacks exons
b) lacks introns
c) can form very large DNA segments
d) contains selectable markers
e) is very easy to isolate

A

b) lacks introns

50
Q

The restriction enzyme EcoRI recognizes the sequence G AATTC. Which of the following is TRUE of DNA after it is treated with EcoRI?

a) Some of the DNA will have single-stranded regions ending in AA and others will end in G.
b) All of the DNA will have blunt ends.
c) All of the DNA fragments will have single-stranded regions ending in G.
d) All of the DNA will be circular.
e) All of the DNA fragments will have single-stranded regions ending in AA.

A

e) All of the DNA fragments will have single-stranded regions ending in AA.

51
Q

Which of the following places the steps in the PCR procedure in the correct order?

1) Incubate at 94 degrees C to denature DNA strands
2) Incubate at 72 degrees C for DNA synthesis
3) Incubate at 60 degrees C for primer hybridization

a) 2, 1, 3
b) 1, 2, 3
c) 3, 2, 1
d) 3, 1, 2
e) 1, 3, 2

A

e) 1, 3, 2

52
Q

Which of the following are used to silence specific genes and hold promise for treating cancer or viral diseases, such as hepatitis B?

a) complentary DNA (cDNA)
b) tumor-inducing plasmids (Ti plasmids)
c) reverse transcriptase PCR (rtPCR)
d) RNA interference (RNAi)
e) DNA fingerprinting

A

d) RNA interference (RNAi)

53
Q

Which of the following techniques is NOT used to introduce recombinant DNA into plants?

a) microinjection
b) gene guns
c) Ti plasmids and Agrobacterium
d) protoplast fusion
e) electroporation

A

a) microinjection

54
Q

In Figure 9.5, the marker genes used for selecting recombinant DNA are

a) ampR and ori
b) ampR and lacZ
c) HindIII, BamHI, and EcoRI
d) lacZ and ori
e) ori

A

b) ampR and lacZ

55
Q

In Figure 9.5, the gene that allows the plasmid to be self-replicating is

a) ori
b) ampR
c) EcoRI
d) lacZ
e) HindIII

A

a) ori

56
Q

Which of the following methods would be used to introduce the plasmid shown in Figure 9.5 into EcoRI?

a) microinjection
b) Ti plasmids and Agrobacterium
c) gene guns
d) transformation

A

d) transformation

57
Q

Gene silencing blocks an undesirable product by

a) blocking transcription
b) making double-stranded RNA.
c) allosteric inhibition of an enzyme.
d) end-product repression.
e) blocking DNA replication.

A

b) making double-stranded RNA.

58
Q

You want to determine whether a person has a mutant gene. The process involves using a primer and a heat-stable DNA polymerase. This process is

a) restriction mapping
b) translation
c) site-directed mutagenesis
d) transformation
e) PCR

A

e) PCR

59
Q

Which of the following are used by the Centers for Disease Control and Prevention to track outbreaks of foodborne disease?

a) DNA fingerprinting
b) restriction fragment length polymorphisms
c) reverse-transcriptase PCR (rtPCR)
d) DNA fingerprings and restriction fragment length polymorphisms
e) DNA fingerprings, restriction length polymorphisms, and reverse transcriptase PCR (rtPCR)

A

e) DNA fingerprings, restriction length polymorphisms, and reverse transcriptase PCR (rtPCR)

60
Q

Assume you have discovered a cell that produces a lipase that works in cold water for a laundry additive. You can increase the efficiency of this enzyme by changing one amino acid. This is done by

a) Selective breeding
b) site-directed mutagenesis
c) enrichment
d) irradiating the cells
e) selection

A

b) site-directed mutagenesis

61
Q

The use of “suicide” genes in genetically modified organisms is designed to

a) delete genes necessary for modified organism’s growth
b) provide a means to eliminate non-modified organisms
c) prevent the growth of the modified organisms in the environment
d) provide for resistance of the modified organisms to pesticides
e) kill the modified organisms before they are released in the environment

A

c) prevent the growth of the modified organisms in the environment

62
Q

In the Southern blot technique, which of the following is NOT required?

a) transfer of DNA to nitrocellulose
b) electrophoresis to separate fragments
c) addition of heat-stable DNA polymerase to amplify DNA
d) addition of a labeled probe to identify the gene of interest
e) restriction of enzyme digestion of DNA

A

c) addition of heat-stable DNA polymerase to amplify DNA

63
Q

The random shotgun method is used in

a) forensic microbiology
b) amplification of unknown DNA
c) transforming plant cells with recombinant DNA
d) genome sequencing
e) RFLP analysis

A

d) genome sequencing

64
Q

Restriction enzymes are

a) animal enzymes that splice RNA
b) bacterial enzymes that splice DNA
c) viral enzymes that destroy host DNA
d) bacterial enzymes that destroy phage DNA

A

d) bacterial enzymes that destroy phage DNA

65
Q

The study of genetic material taken directly from the environment is

a) proteomics
b) forensic microbiology
c) metagenomics
d) bionfirmatics
e) reverse genetics

A

c) metagenomics

66
Q

True/False
The term biotechnology refers exclusively to the use of genetically engineered organisms for the production of desired products.

A

False

67
Q

T/F In recombinant DNA technology, a vector is a self-replicating segment of DNA, such as plasmid or viral genome.

A

True

68
Q

T/F The practice of breeding plants and animals for desirable traits, such as high crop yield, is called natural selection.

A

False