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प्रश्न
Why is the coding sequence of an enzyme β-galactosidase a preferred selectable marker in comparison to the ones named above?
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उत्तर १
The gene for the enzyme β-galactosidase is an alternative selectable marker. When the foreign gene is inserted within the β-galactosidase gene, the enzyme β- galactosidase gets inactivated. Then the bacteria are grown on a chromogenic substrate. Non-recombinants will produce blue-coloured colonies, while recombinants will produce colourless colonies.
उत्तर २
The coding sequence of the enzyme β-galactosidase is a preferred selectable marker compared to antibiotic resistance markers like those in pBR322 because it simplifies the identification of recombinants. Antibiotic-based selection is cumbersome as it requires plating on multiple antibiotic-containing media. In contrast, insertional inactivation of β-galactosidase allows differentiation based on colour. When recombinant DNA is inserted within the β-galactosidase gene, it inactivates the enzyme, resulting in colourless colonies on media with a chromogenic substrate, while non-recombinants produce blue colonies. This visual distinction makes β-galactosidase an efficient and convenient selectable marker for identifying transformants.
संबंधित प्रश्न
State how has Agrobacterium tumifaciens been made a useful cloning vector to transfer DNA to plant cells.
Answer the following question.
Expand ‘YAC’ and mention what it was used for.
Which of the following statement is not true for a clone?
Plasmids are suitable vectors for gene cloning because these ______.
Plasmid pBR322 has a PstI restriction enzyme site within gene ampR that confers ampicillin resistance. If this enzyme is used for inserting a gene for β-galactoside production and the recombinant plasmid is inserted in an E.coli strain.
What does ‘competent’ refer to in competent cells used in transformation experiments?
For selection of recombinants, insertional inactivation of antibiotic marker has been superceded by insertional inactivation of a marker gene coding for a chromogenic substrate. Give reasons.
Describe the role of Agrobacterium tumefaciens in transforming a plant cell.
Which of the following enzyme(s) are NOT essential for gene cloning?
- Restriction enzymes
- DNA ligase
- DNA mutase
- DNA recombinase
- DNA polymerase
Choose the correct answer from the options given below:
The following diagram showing restriction sites in E. coli cloning vector pBR322. Find the role of ‘X’ and ‘Y’ genes:

