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What is polymerase chain reaction (PCR)? - Biology

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प्रश्न

What is polymerase chain reaction (PCR)?

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अति संक्षिप्त उत्तर
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उत्तर १

Polymerase chain reaction (PCR) is another device used for gene cloning or gene multiplication in vitro.

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उत्तर २

Polymerase Chain Reaction (PCR) is an in vitro technique used to generate millions of copies of a specific DNA segment rapidly. PCR involves three main steps repeated in cycles: denaturation (heating DNA to separate strands), annealing (binding of primers to target DNA), and extension (DNA polymerase synthesizes new DNA). The enzyme used is Taq polymerase, which is heat-stable and derived from Thermus aquaticus. PCR amplifies DNA to make numerous copies from a small initial sample, facilitating genetic research and diagnostics.

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अध्याय 13: Principles and Processes of Biotechnology - BOARD EXAMINATION QUESTIONS [पृष्ठ ५३३]

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नूतन Biology [English] Class 12 ISC
अध्याय 13 Principles and Processes of Biotechnology
BOARD EXAMINATION QUESTIONS | Q 10. a. | पृष्ठ ५३३

संबंधित प्रश्न

Explain the properties of a good or ideal cloning vector for rDNA technology.


Match the List I with List II and List ill. Select the correct option.

  List I   List II   List ill
i. Hind III a. Agarose ge 1. Six base pairs
ii. pBR322 b. Agrobacterium 2. Selectable marke
iii. T-DNA c. Ampicillin 3. Elution
iv. DNA d. Recognition sequenc 4. Transgenic  plant

The time taken to complete one cycle of PCR is around ______.


Which of the following device is required for PCR?


Nucleic acid segment tagged with a radioactive molecule is called ______.


Name a recombinant vaccine that is currently being used in vaccination programme.


What would happen when one grows a recombinant bacterium in a bioreactor but forget to add antibiotic to the medium in which the recombinant is growing?


Name the plant disease caused by Agrobacterium tumefaciens.


Oil spill is a major environmental issue. It has been found that different strains of Pseudomonas bacteria have genes to break down the four major groups of hydrocarbons in oil. Trials are underway to use different biotechnological tools to incorporate these genes and create a genetically engineered strain of Pseudomonas - a ‘super-bug’, to break down the four major groups of hydrocarbons in oil. Such bacteria might be sprayed onto surfaces polluted with oil to clean thin films of oil.

(a) List two advantages of using bacteria for such biotechnological studies?

(b) For amplification of the gene of interest PCR was carried out. The PCR was run with the help of polymerase which was functional only at a very low temperature. How will this impact the efficiency of the PCR? Justify.

(c) If such bacteria are sprayed on water bodies with oil spills, how will this have a positive or negative effect on the environment? Discuss.


Restriction enzymes were discovered by ______.


Which of the following enzyme catalyses the removal of nucleotides from the end of DNA molecules?


The given figure is the diagrammatic representation of the E. coli vector pBR322. Which one of the given options correctly indentites its certain component(s)?


How does EcoRI differ from an exonuclease?


Name the enzyme responsible for the transcription of genetic code to produce mRNA.


In vitro amplification of DNA segments is called______.


Expand YAC used in the field of Biotechnology.


Which one of the following enzymes is used to join DNA fragments? 


State the steps involved in the process of gene therapy for the treatment of ADA-deficiency.


David is a molecular biologist. He uses a technique to know the amino acids occupy the first and the last positions in the Chain - A and Chain - B of insulin. Name the scientist whose contribution made it possible for David to use this technique.


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