हिंदी

Name the enzymes that are used for the isolation of DNA from bacterial and fungal cells for recombinant DNA technology.

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प्रश्न

Name the enzymes that are used for the isolation of DNA from bacterial and fungal cells for recombinant DNA technology.

अति संक्षिप्त उत्तर
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उत्तर

Lysozyme is used for the isolation of DNA from bacterial cells, chitinase is used for the isolation of DNA from fungal cells and cellulase is used for the isolation of DNA from plant cells.

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अध्याय 11: Principles and Processes of Biotechnology - Test Your Progress [पृष्ठ ५३२]

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नूतन Biology [English] Class 12 ISC
अध्याय 11 Principles and Processes of Biotechnology
Test Your Progress | Q 8. | पृष्ठ ५३२

संबंधित प्रश्न

How does a restriction nuclease function? Explain


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


Explain briefly:

Restriction enzymes and DNA


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


The DNA fragment separated on an agarose gel can be visualized by staining with ______.


DNA strands on a gel stained with ethidium bromide when viewed under UV radiation, appear as ______


Which of the following enzymes catalyse the removal of nucleotides from the ends of DNA?


Which of the following bacteria is not a source of restriction endonuclease?


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


CTTAAG
GAATTC

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

Given below is the stepwise schematic representation of the process of electrophoresis. Identify the 'alphabets' representing 

  1. Anode end
  2. smallest/lightest DNA strand in the matrix
  3. Agarose gel


State the importance of elution in this process.


'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.

How are DNA fragments visualised once they are separated by gel electrophoresis?


How do exonucleases differ fundamentally from endonucleases in their enzymatic site of action?


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?


What is the origin of agarose, the matrix most commonly used in gel electrophoresis?


According to the sieving effect of an agarose gel matrix, which DNA fragments move the farthest and fastest from the loading wells?


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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