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

Explain briefly: Chitinase

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प्रश्न

Explain briefly:

Chitinase

स्पष्ट करा
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उत्तर

Chitinase is a class of enzymes used for the degradation of chitin, which forms a significant component of the fungal cell wall. Therefore, to isolate the DNA enclosed within the cell membrane of the fungus, the enzyme chitinase is used to break the cell to release its genetic material.

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पाठ 9: Biotechnology : Principles and Processes - EXERCISES [पृष्ठ १७६]

APPEARS IN

एनसीईआरटी Biology [English] Class 12
पाठ 9 Biotechnology : Principles and Processes
EXERCISES | Q 11. (c) | पृष्ठ १७६
नूतन Biology [English] Class 12 ISC
पाठ 11 Principles and Processes of Biotechnology
NCERT EXERCISES WITH ANSWERS | Q 10. (c) | पृष्ठ ५३६

संबंधित प्रश्‍न

Name two commonly used bioreactors.


Suggest and describe a technique to obtain multiple copies of a gene of interest in vitro.


Draw a labelled sketch of sparged-stirred-tank bioreactor. Write its application.


Can you list 10 recombinant proteins which are used in medical practice? Find out where they are used as therapeutics (use the internet).


Explain briefly:

PCR


State the importance of using a bioreactor.


Describe the process of amplification of the “gene of interest” using the PCR technique.


Which of the following term used for defining a viral genome incorporated into host DNA?


DNA fragments generated by the restriction endonuclease in a chemical reaction can be separated by ______.


PCR and restriction fragment length polymorphism are the methods for ______.


A single strand of nucleic acid tagged with a radioactive molecule is called ______.


PCR proceeds mthree distinct steps governed by temperature, they are in order of ______.


In addition to the Taq polymerase enzyme, which other thermostable DNA polymerases have been isolated to be used in PCR?


Which of the following steps are catalysed by Taq DNA polymerase in a PCR reaction?


A bacterial cell was transformed with a recombinant DNA molecule that was generated using a human gene. However, the transformed cells did not produce the desired protein. Reasons could be ______.


Which of the following should be chosen for best yield if one were to produce a recombinant protein in large amounts?


How is copy number of the plasmid vector related to yield of recombinant protein?


While doing a PCR, ‘denaturation’ step is missed. What will be its effect on the process?


Do biomolecules (DNA, protein) exhibit biological activity in anhydrous conditions?


Identify and explain steps ‘A’, ‘B’ and ‘C’ in the PCR diagram given below.


Illustrate the design of a bioreactor. Highlight the difference between a flask in your laboratory and a bioreactor which allows cells to grow in a continuous culture system.


Read the following paragraph and answer the questions that follow:

Biotechnology revolves around the "gene of interest", with an objective to open various avenues for human welfare in health, medicine, pharma, agriculture etc. using different techniques, tools and processes. One of the breakthroughs of biotechnology in medicine is the gene therapy.
  1. Name the human disease for which the gene therapy was used for the first time.
  2. Explain the steps of gene therapy carried to cure the disease using the lymphocytes of the patient. Why is this therapy not a permanent cure of the disease?
  3. Write the possible permanent cure of the disease by the gene therapy that is in progress. 

Given below are two statements:

Statement I: The DNA fragments extracted from gel electrophoresis can be used in construction of recombinant DNA.

Statement II: Smaller size DNA fragments are observed near anode while larger fragments are found near the wells in an agarose gel.

In the light of the above statements, choose the most appropriate answer from the options given below:


Which of the following statements is incorrect?


Main steps in the formation of Recombinant DNA are given below. Arrange these steps in a correct sequence.

  1. Insertion of recombinant DNA into the host cell.
  2. Cutting of DNA at specific location by restriction enzyme.
  3. Isolation of desired DNA fragment.
  4. Amplification of gene of interest using PCR. 

Choose the correct answer from the options given below:


What is the primary definition of recombinant DNA technology?


Which enzymes act as 'molecular scissors' to cut purified DNA precisely at specific target sites?


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