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A source of heat- stable DNA polymerase is


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

F) None of the above
G) B) and E)

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


A) Bacillus thuringiensis insecticide
B) Nitrogenase (nitrogen fixation)
C) Glyphosate resistance
D) Drought resistance
E) Frost retardant

F) B) and E)
G) A) and D)

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A colleague has used computer modeling to design an improved enzyme. To produce this enzyme, the next step is


A) Determine the nucleotide sequence for the improved enzyme.
B) Synthesize the gene for the improved enzyme.
C) Mutate bacteria until one makes the improved enzyme.
D) Look for a bacterium that makes the improved enzyme.
E) None; the enzyme can't be produced.

F) C) and D)
G) A) and B)

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If you have inserted a gene in the Ti, the next step in genetic engineering is


A) Splicing Ti into a plasmid.
B) Transformation of E. coli with Ti.
C) Transformation of an animal cell.
D) Inserting Ti into Agrobacterium.
E) None of the above.

F) A) and C)
G) A) and B)

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Figure 9.3 Figure 9.3    -In Figure 9.3, the resulting organism (a)  is A)  Pseudomonas fluorescens. B)  a plant × Pseudomonas hybrid. C)  Bacillus thuringiensis. D)  E. coli. E)  A tomato plant. -In Figure 9.3, the resulting organism (a) is


A) Pseudomonas fluorescens.
B) a plant × Pseudomonas hybrid.
C) Bacillus thuringiensis.
D) E. coli.
E) A tomato plant.

F) A) and B)
G) C) and D)

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Which organism naturally possesses the Ti plasmid?


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

F) B) and C)
G) A) and C)

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Which organism degrades PCBs and has been engineered to produce BT toxin?


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

F) None of the above
G) A) and C)

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Which of the following can be used to make recombinant DNA?


A) Protoplast fusion
B) Tungsten "bullets"
C) Transformation
D) Microinjection
E) All of the above.

F) A) and D)
G) A) and E)

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PCR can be used to identify an unknown bacterium because


A) DNA can be electrophoresed.
B) All cells have DNA.
C) DNA polymerase will replicate DNA.
D) The RNA primer is specific.
E) None of the above.

F) A) and B)
G) A) and C)

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Large numbers of bacterial cells are not found in crown galls because


A) The assumption is not true; many bacteria are in the galls.
B) A gene in plant cells is controlling growth.
C) The plant kills the bacteria.
D) Cell walls protect the plant from bacterial invasion.
E) None of the above.

F) B) and E)
G) A) and D)

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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) 1, 2, 3, 5, 4, 7, 6
B) 6, 7, 2, 3, 4, 5, 1
C) 6, 2, 1, 3, 4, 5, 7
D) 5, 2, 3, 4, 7, 6, 1
E) 6, 7, 2, 4, 5, 3, 1

F) C) and E)
G) D) and E)

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Figure 9.3 Figure 9.3    -In Figure 9.3, the purpose of this experiment is to A)  Put a gene in Bacillus. B)  Put a gene into a plant. C)  Put an insecticide on plant leaves. D)  Isolate Pseudomonas from a plant. E)  None of the above. -In Figure 9.3, the purpose of this experiment is to


A) Put a gene in Bacillus.
B) Put a gene into a plant.
C) Put an insecticide on plant leaves.
D) Isolate Pseudomonas from a plant.
E) None of the above.

F) B) and C)
G) None of the above

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Which of the following is not involved in making cDNA?


A) Transcription.
B) RNA processing to remove introns.
C) Reverse transcription.
D) Translation.

E) All of the above
F) C) and D)

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The use of an antibiotic resistance gene on a plasmid used in genetic engineering makes


A) The recombinant cell unable to survive.
B) Replica plating possible.
C) Direct selection possible.
D) The recombinant cell dangerous.
E) All of the above.

F) None of the above
G) A) and E)

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PCR can be used to amplify DNA in a clinical sample. The following steps are used in PCR. What is the fourth step?


A) Incubate at 72°C.
B) Collect DNA.
C) Incubate at 94°C.
D) Incubate at 60°C.
E) Add DNA polymerase.

F) None of the above
G) A) and B)

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Foreign DNA can be inserted into cells by all of the following except


A) A gene gun.
B) Electroporation.
C) Transformation.
D) Protoplast fusion.
E) None of the above.

F) A) and D)
G) A) and C)

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

F) C) and D)
G) A) and B)

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Suicide genes can be controlled by the fimbriae- gene operator. This would result in the death of


A) Cells at 37°C.
B) All cells.
C) Cells making fimbriae.
D) Conjugating cells.
E) Cells making flagella.

F) A) and B)
G) D) and E)

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The reaction catalyzed by DNA polymerase.


A) mRNA -cDNA
B) DNA -mRNA
C) mRNA -protein
D) DNA -DNA
E) None

F) All of the above
G) B) and E)

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Figure 9.1 Figure 9.1    -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)  3.00 kbp C)  0.25 kbp D)  1.50 kbp E)  1.08 kbp -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) 3.00 kbp
C) 0.25 kbp
D) 1.50 kbp
E) 1.08 kbp

F) All of the above
G) C) and D)

Correct Answer

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