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कर्नाटक बोर्ड पी.यू.सी.पीयूसी विज्ञान 2nd PUC Class 12

Would you choose an exonuclease while producing a recombinant DNA molecule?

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प्रश्न

Would you choose an exonuclease while producing a recombinant DNA molecule?

Would you like to choose an exonuclease enzyme while producing a recombinant DNA molecule?

अति संक्षिप्त उत्तर
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उत्तर

No, as exonuclease acts on the free ends of linear DNA molecule. Therefore, instead of producing DNA fragments with sticky ends, it will shorten or completely degrade the DNA fragment containing the gene of interest, and the circular plasmid (vector) will not get cut as it lacks free ends.

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अध्याय 11: Biotechnology : Principles and Processes - VERY SHORT ANSWER [पृष्ठ ७८]

APPEARS IN

एनसीईआरटी एक्झांप्लर Biology Exemplar [English] Class 12
अध्याय 11 Biotechnology : Principles and Processes
VERY SHORT ANSWER | Q 2. | पृष्ठ ७८
नूतन Biology [English] Class 12 ISC
अध्याय 11 Principles and Processes of Biotechnology
Test Your Progress | Q 21. | पृष्ठ ५३३

संबंधित प्रश्न

How does a restriction nuclease function? Explain


Make a chart (with diagrammatic representation) showing a restriction enzyme, the substrate DNA on which it acts, the site at which it cuts DNA and the product it produces.


Collect 5 examples of palindromic DNA sequences. Better try to create a palindromic sequence by following base-pair rules.


Distinguish between exonuclease and endonuclease.


Give a reason why :
Single cloning site is preferred in a vector.


The total number of nucleotide sequences of DNA that code for a hormone is 1530. The proportion of different bases in the sequence is found to be Adenine = 34%, Guanine = 19%, Cytosine = 23%, Thymine = 19%.

Applying Chargaff’s rule, what conclusion can be drawn?


Restriction enzymes ______.


There is a restriction endonudease called as EcoRI. What does co part in it stands for?


Molecular scissors, which cut DNA at specific site is ______.


'Restriction' in restriction enzyme refers to


In agarose gel electrophoresis, DNA molecules are separated on the basis of their ______.


Restriction enzymes that are used in the construction of recombinant DNA are endonucleases which cut the DNA at ‘specific-recognition sequence’. What would be the disadvantage if they do not cut the DNA at specific-recognition sequence?


A mixture of fragmented DNA was electrophoresed in an agarose gel. After staining the gel with ethidium bromide, no DNA bands were observed. What could be the reason?


CTTAAG
GAATTC

  1. What are such sequences called? Name the enzyme used that recognizes such nucleotide sequences.
  2. What is their significance in biotechnology?

What is elution?


State the importance of elution in this process.


Given below is the restriction site of a restriction endonuclease Pst-I and the cleavage sites on a DNA molecule.

\[\ce{5' C - T - G - C - A \overset{\downarrow}{-}{G 3'}}\]

\[\ce{3' G\underset{\uparrow}{-} A - C - G - T - C 5'}\]

Choose the option that gives the correct resultant fragments by the action of the enzyme Pst-I.


'EcoRI' has played a very significant role in rDNA technology.

  1. Explain the convention for naming EcoRI.
  2. Write the recognition site and the cleavage sites of this restriction endonuclease.

What are the protruding and hanging stretches of DNA produced by these restriction enzymes called? Describe their role in the formation of rDNA.


State the principle involved in separation of DNA fragments using gel electrophoresis.


What is the precise definition of a palindromic sequence in DNA?


Which of the following was the very first restriction endonuclease to be isolated and characterized?


In the standard nomenclature convention for restriction endonucleases, what do the second and third letters signify?


Which of the following represents the specific palindromic recognition sequence cleaved by the restriction endonuclease EcoRI?


Why is it mandatory to cut both the vector DNA and the foreign source DNA with the exact same restriction enzyme when constructing recombinant DNA?


How are separated DNA bands visualized following agarose gel electrophoresis?


What is the process called when desired, separated DNA bands are physically cut out from the agarose gel and extracted from the gel piece?


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