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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
A clone is a ______.
A suitable vector for gene cloning in higher organism is ______.
Describe the role of CaCl2 in the preparation of competent cells?
Describe the role of Agrobacterium tumefaciens in transforming a plant cell.
The following diagram showing restriction sites in E. coli cloning vector pBR322. Find the role of ‘X’ and ‘Y’ genes:

Which of the following is not a cloning vector?
What is the primary function of a vector in recombinant DNA technology?
What is the basic biological nature of plasmids when used as cloning vectors?
Which of the following describes the function of a selectable marker in a cloning vector?
Which vector derived from \(\textit{Agrobacterium tumefaciens}\) is utilized for delivering foreign genes into plants?
