Question:

In the process of insertional inactivation

Updated On: Jul 6, 2022
  • a recombinant $DNA$ is inserted within the coding sequence of enzyme $\beta$-galactosidase, resulting in inactivation of the enzyme
  • a recombinant $DNA$ is inserted within the coding sequence of proteins involved in the replication of the plasmid
  • a recombinant $DNA$ is inserted within the recognition site for EcoRI
  • none of the above
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The Correct Option is A

Solution and Explanation

Alternative selectable markers have been developed which differentiate recombinants from the non-recombinants on the basis of their ability to produce colour in the presence of a chromogenic substrate. In this, a recombinant $DNA$ is inserted within the coding sequence of an enzyme, $p$-galactosidase. This results into inactivation of the enzyme, which is referred to as insertional inactivation. The presence of a chromogenic substrate gives blue coloured colonies if the plasmid in the bacteria does not have an insert. Presence of insert results into insertional inactivation of the $P$-galactosidase and the colonies do not produce any colour, these are identified as recombinant colonies.
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Concepts Used:

Biotechnology

Biotechnology is a vast field of biology that involves the creation, production, and modification of useful products for human welfare using both the technology and the execution of living organisms and their components. An agricultural engineer, Karoly Ereky, coined the word "biotechnology" in 1919, achieving him the title of "Father of Biotechnology."

Principles of Biotechnology:

Among many, the two core techniques that entitled the birth of modern biotechnology are :

  1. Genetic Engineering is one of the methods of direct modifications of an organism's genome (i.e., DNA and RNA). It requires the introduction of new genes into host species to escalate function or trait, hence altering the host organism's phenotype.
  2. Bioprocess Engineering is one of the methods of maintaining sterile conditions to facilitate the growth of large quantities of desired microbes and other eukaryotic cells for the development of new or modified biotechnological products such as enzymes, vaccines, antibiotics, and other biotechnological products.