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प्रश्न
| Oil spill is a major environmental issue. It has been found that different strains of Pseudomonas bacteria have genes to break down the four major groups of hydrocarbons in oil. Trials are underway to use different biotechnological tools to incorporate these genes and create a genetically engineered strain of Pseudomonas - a ‘super-bug’, to break down the four major groups of hydrocarbons in oil. Such bacteria might be sprayed onto surfaces polluted with oil to clean thin films of oil. |
(a) List two advantages of using bacteria for such biotechnological studies?
(b) For amplification of the gene of interest PCR was carried out. The PCR was run with the help of polymerase which was functional only at a very low temperature. How will this impact the efficiency of the PCR? Justify.
(c) If such bacteria are sprayed on water bodies with oil spills, how will this have a positive or negative effect on the environment? Discuss.
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उत्तर
(a) You can easily grow a large quantity of the bacteria/no ethical issues/have plasmids/can easily transform.
(b) PCR will not amplify the gene.
If the polymerase enzyme denatures at low temperatures, it will not be able to withstand high temperatures which is essential for separating/opening/unwinding/denaturing DNA strands to open. Thus subsequent step of extending the primers using the nucleotides provided in the reaction and the genomic DNA as the template will not occur.
(c) Positive effect: Oil spills can be treated and the environment becomes better/cleaner/water becomes more potable/safe for aquatic forms/safe for water birds like seagulls.
Negative effect: The bacteria can mutate/can harm other organisms/can conjugate with other non-virulent forms and make them super-bugs with detrimental effects/unpredictable/for a longer duration it may reduce the dissolved oxygen and lead to mortality of aquatic organisms.
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संबंधित प्रश्न
Distinguish between RNA and DNA.
Expand the following abbreviation: BAC
Identify the CORRECT sequence of steps in PCR.
DNA polymerase enzyme used in PCR is isolated from ____________ bacteria.
Following are the four statements regarding separation of DNA fragments using Gel electrophoresis. Identify the INCORRECT statements.
i. DNA is negatively charged molecule and so it is loaded on gel towards the Anode terminal.
ii. DNA fragments travel along the surface of the gel whose concentration does not affect movement of DNA.
iii. Smaller the size of DNA fragment, larger is the distance it travels through it.
iv. Pure DNA can be visualized directly by exposing to UV radiation.
In PCR technique, the organism providing thermostable DNA polymerase is a ____________.
The most important feature in a plasmid to serve as a vector in gene cloning experiment is ______.
What is the significance of adding proteases at the time of isolation of genetic material (DNA)?
Write steps involved in gene amplification.
Name the enzyme responsible for the transcription of genetic code to produce mRNA.
