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

From what you have learnt, can you tell whether enzymes are bigger or DNA is bigger in molecular size? How did you know?

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प्रश्न

From what you have learnt, can you tell whether enzymes are bigger or DNA is bigger in molecular size? How did you know?

लघु उत्तर
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उत्तर

Both DNA (deoxyribonucleic acid) and enzymes are macromolecules. DNA is a polymer of deoxyribonucleotides, and enzymes are proteins; hence, these are polymers of amino acids. But DNA is larger in molecular size than proteins because protein synthesis is regulated by small segments of DNA, called genes, and a single DNA molecule can encode many proteins.

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पाठ 9: Biotechnology : Principles and Processes - EXERCISES [पृष्ठ १७५]

APPEARS IN

एनसीईआरटी Biology [English] Class 12
पाठ 9 Biotechnology : Principles and Processes
EXERCISES | Q 3. | पृष्ठ १७५
नूतन Biology [English] Class 12 ISC
पाठ 11 Principles and Processes of Biotechnology
NCERT EXERCISES WITH ANSWERS | Q 3. | पृष्ठ ५३५

संबंधित प्रश्‍न

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.


Explain briefly:

Chitinase


Answer the following question:
Describe the formation of recombinant DNA by the action of EcoRI.


In a pathological lab, a series of steps were undertaken for finding the gene of interest. Describe the steps, or make a flow chart showing the process of amplification of this gene of interest.


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


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


The first step in recombinant DNA technology is


Rising of dough is due to ______.


Which of the following contributed in popularising the PCR (polymerase chain reactions) technique?


Significance of 'heat shock' method in bacterial transformation is to facilitate ______.


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


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. 

Write the scientific name of the source organism of the thermostable DNA polymerase used in PCR.


Bioreactors are the containment vehicles of any biotechnology-based production process. For large scale production and for economic reasons the final success of biotechnological process depends on the efficiency of the bioreactor.

Answer the following questions w.r.t. the given paragraph:

  1. List the operational guidelines that must be adhered to so as to achieve optimisation of the bioreactor system. Enlist any four.
  2. Mention the phase of the growth we refer to in the statement "Optimisation of growth and metabolic activity of the cells".
  3. Is the biological product formed in the bioreactor suitable for the intended use immediate? Give reason in support of your answer.

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:


Upon exposure to UV radiation, DNA stained with ethidium bromide will show ______.


What is the primary definition of recombinant DNA technology?


In agarose gel electrophoresis, why do DNA fragments move toward the positive electrode?


What is the process of cutting out and recovering a separated DNA band from an agarose gel called?


In the provided agarose gel electrophoresis image, what is represented in lane 1 compared to lanes 2 through 4?


Which enzyme is responsible for joining the desired gene to a carrier vector DNA to form recombinant DNA?


How are bacterial cells typically made competent to facilitate the uptake of recombinant DNA during transformation?


Which of the following are direct methods used for introducing recombinant DNA into host cells besides chemical transformation?


Which series of operations is collectively referred to as 'downstream processing'?


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