1. | To replicate DNA fragments rapidly. |
2. | To cut DNA into smaller fragments using restriction enzymes. |
3. | To separate DNA fragments based on their size. |
4. | To join fragments of DNA from different sources. |
1. | Quickly synthesize small DNA fragments for gene therapy. |
2. | Amplify large quantities of DNA from a small sample. |
3. | Cut specific DNA fragments for cloning. |
4. | Directly insert genes into living cells. |
1. | Provide the starting point for DNA synthesis. |
2. | Help in cutting the DNA into smaller fragments. |
3. | Join the DNA fragments after amplification. |
4. | Act as selectable markers. |
1. | Adding alcohol to precipitate the DNA. |
2. | Heating the cell to denature DNA. |
3. | Using enzymes to cut the DNA into smaller fragments. |
4. | Exposing the cell to ultraviolet light. |
Assertion (A): | Downstream processing is vital in biotechnology for the purification of products. |
Reason (R): | It ensures that the products are of high purity and quality, suitable for industrial and clinical use. |
1. | Both (A) and (R) are True and (R) is the correct explanation of (A) |
2. | Both (A) and (R) are True but (R) is not the correct explanation of (A) |
3. | (A) is True but (R) is False |
4. | (A) is False but (R) is True |
Assertion (A): | A continuous culture is likely to produce more biomass in industrial production of recombinant products |
Reason (R): | In continuous culture, the microbes are continuously kept in their log phase of growth. |
1. | Both (A) and (R) are True and (R) correctly explains (A) |
2. | Both (A) and (R) are True but (R) does not correctly explain (A) |
3. | (A) is True, (R) is False |
4. | (A) is False, (R) is True |
Column I | Column II | ||
A. | DNA polymerase | 1. | Joining DNA fragments |
B. | Restriction endonuclease | 2. | Synthesizes new strands of DNA |
C. | DNA ligase | 3. | Cuts DNA at specific sequences |
D. | Reverse transcriptase | 4. | Synthesizes DNA from RNA template |
1. | amplifying DNA in the polymerase chain reaction (PCR). |
2. | creation of blunt ends in digested DNA fragments. |
3. | artificial synthesis of DNA in a template independent manner. |
4. | proof reading of newly synthesized DNA strands. |
1. | Thomas Cech | 2. | Fred Sanger |
3. | Kary Mullis | 4. | Millstein and Kohler |