Plasmids/Vectors Flashcards

1
Q

What is a plasmid?

A

A plasmid is a small, circular, double-stranded DNA molecule found in bacteria that can replicate independently of chromosomal DNA and often carries beneficial genes.

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2
Q

What is a vector in genetic engineering?

A

A vector is an artificially made DNA molecule that facilitates the incorporation of foreign DNA for manipulation and replication.

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3
Q

What are restriction endonucleases?

A

Enzymes that cleave DNA molecules at specific recognition sequences, producing fragments useful for genetic engineering.

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4
Q

How do bacterial cells take up plasmids?

A

Through transformation, which can be induced by heat shock or electroporation.

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5
Q

What is recombinant DNA technology?

A

A method used to insert foreign genes into plasmids, allowing bacteria to express desired proteins.

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6
Q

Plasmids are used as cloning vectors in

A

biotechnology.

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7
Q

Restriction enzymes cut DNA at specific sites, allowing

A

gene insertion.

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8
Q

The origin of replication (OR) enables

A

plasmid self-replication.

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9
Q

The lacZ gene is used in

A

blue/white screening for successful gene cloning.

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10
Q

Recombinant insulin was first commercially produced using

A

genetically modified E. coli.

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11
Q

Plasmids always integrate into the bacterial genome.

A

False – Most plasmids replicate independently.

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12
Q

Electroporation uses an electric current to increase DNA uptake.

A

True.

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13
Q

All restriction enzymes cut DNA at random locations.

A

False – They cut at specific recognition sequences.

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14
Q

Cloning vectors can carry genes for antibiotic resistance.

A

True.

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15
Q

The enzyme responsible for linking DNA fragments together is called __________.

A

A: DNA ligase.

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16
Q

A bacterium capable of taking up foreign DNA is said to be __________.

A

A: Competent.

17
Q

The method of screening recombinant bacteria using the lacZ gene is called __________ screening.

A

A: Blue/white.

18
Q

The two common methods for inducing bacterial transformation are __________ and __________.

A

A: Heat shock, electroporation.

19
Q

What is the function of a multiple cloning site in a plasmid?
A) Protect the bacterial chromosome
B) Provide multiple restriction sites for gene insertion
C) Prevent transformation
D) Enhance bacterial metabolism

A

A: B) Provide multiple restriction sites for gene insertion.

20
Q

Which of the following is NOT a feature of plasmids used in genetic engineering?
A) Origin of replication
B) Antibiotic resistance gene
C) Mitochondrial DNA
D) Restriction enzyme sites

A

A: C) Mitochondrial DNA.

21
Q

What is a common bacterial host for cloning plasmids?
A) Staphylococcus aureus
B) Escherichia coli
C) Saccharomyces cerevisiae
D) Mycobacterium tuberculosis

A

A: B) Escherichia coli.

22
Q

What is a key step in recombinant insulin production?
A) Inserting the human insulin gene into a bacterial plasmid
B) Using bacteria to synthesize viral proteins
C) Growing human cells in a bioreactor
D) Producing insulin in fungal spores

A

A: A) Inserting the human insulin gene into a bacterial plasmid.

23
Q

A researcher uses restriction enzymes to cut a plasmid and insert a foreign gene. What enzyme is needed to join the fragments?

A

A: DNA ligase.

24
Q

A scientist introduces a plasmid containing an antibiotic resistance gene into bacteria. How can they confirm successful transformation?

A

A: Grow bacteria on antibiotic-containing media to select for transformed cells.

25
A genetic engineer needs bacteria to produce a human protein. What essential plasmid feature should they include?
A: A strong promoter for gene expression.
26
Define transformation in bacterial genetics:
The process by which exogenous DNA is introduced into a bacterial cell and replicated.
27
Define gene cloning:
The process of isolating and amplifying a specific DNA sequence using plasmids.
28
Define restriction digest:
A laboratory technique where restriction enzymes cut DNA at specific sites.
29
Define recombinant protein production:
The process of using genetically modified organisms to synthesize specific proteins for medical and industrial use.