Advertisements
Advertisements
प्रश्न
Why is the coding sequence of an enzyme β-galactosidase a preferred selectable marker in comparison to the ones named above?
Advertisements
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
Write the role of ‘restriction sites’ in the cloning vector pBR322.
Explain the importance of ‘Selectable marker’, with the help of a suitable example.
Answer the following question.
β galactosidase enzyme is considered a better selectable marker. Justify the statement.
Answer the following question.
Expand ‘YAC’ and mention what it was used for.
Which of the following is correctly matched?
Which of the following statement is not true for a clone?
A suitable vector for gene cloning in higher organism is ______.
Which of the following is not a genetic vector?
Describe the role of CaCl2 in the preparation of competent cells?
For selection of recombinants, insertional inactivation of antibiotic marker has been superceded by insertional inactivation of a marker gene coding for a chromogenic substrate.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.
