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Byju's Answer
Standard XII
Biology
What is PCR
Any recombina...
Question
Any recombinant DNA with a desired gene is required in billion copies for commercial use. How is the amplification done? Explain.
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Solution
1. Amplification refers to the process of making multiple copies of the DNA segment in vitro.
2. It employs polymerase chain reaction (PCR).
3. The process was designed by K.Mullis.
4. This technique involves three main steps :
Denaturation
Primer annealing and
Extension of primers.
5. The double-stranded DNA is denatured by using high temperature.
6. Two sets of primers are used.Primers are the chemically synthesized short segments of DNA that are complementary to the segment of DNA.
7. DNA polymerase is the enzyme used to make copies of DNA by using the genomic template DNA and the primer.
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Q.
Arrange the given steps involved in recombinant DNA technology in the correct order.
A. Amplification of desired DNA sequence (gene of interest) with PCR modification
B. Ligation of gene of interest with the vector
C. Removal of RNA and proteins to purify DNA
D. Insertion of recombinant DNA into the host
E. Treatment of cell with cell wall digesting enzyme followed by disruption of the cell membrane
F. Digestion of DNA of interest and vector with suitable restriction enzyme
Q.
Given below are the steps of recombinant DNA technology.
(A) Introduction of desired gene into the host
(B) Identification of desired gene
(C) Transfer of desired gene to the progeny
(D) Isolation of desired gene
(E) Maintenance of introduced DNA into the host
Choose the correct sequence of events.
Q.
How is the amplification of gene done using the technique of PCR? Explain with the help of diagram.
Q.
Tom was trying to isolate a human gene (X) responsible for producing an enzyme (Y). His target was to synthesize Y on a large scale for commercial utility. Mention the correct order of the steps that he needs to perform in order to isolate his gene of interest.
I. Obtaining cell sample from desired tissue
II. Separation of desired DNA by gel electrophoresis
III. Cell lysis
IV. Amplification of desired DNA sequence by PCR
V. Isolation of genomic DNA
VI. Identification of desired band, cutting and elution of DNA from gel
Q.
Write any four ways used to introduce a desired DNA segment into a bacterial cell in recombinant technology experiments.
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