Briefly describe the various stages of recombination DNA technology of genetic engineering and its applications.

Explanation

Recombinant DNA Technology
Genetic engineering is alternately called as recombinant DNA technology or gene cloning. Paul Berg (1972) was awarded Nobel Prize in 1980 and is considered as father of genetic engincering. The first recombinant DNA (DNA) was constructed by Stanley Cohen and Herbert Boyer in 1972.
Recombinant DNA technology involves the following steps
(i) Isolation of the genetic material (DNA) is carried out as follows
(a) DNA is enclosed within the membranes. To release DNA along with other macromolecules -such as RNA, proteins, polysaccharides and lipids, bacterial cells/plant or animal tissue are treated with enzymes such as lysozyme (bacteria), cellulase (plant cells), chitinasc(fungus).
(b) Other molecules can be removed by appropriate treatments and purified DNA ultimately precipitates out as fine threads in the suspension after the addition of chilled ethanol.
(ii) Cutting of DNA at specific locations is done by using restriction enzymes. The purified DNA is incubated with the specific restriction enzyme at conditions optimum for the enzyme to act.
(iii) Isolation of desired DNA fragment is carried out using agarose gel electrophoresis.
(iv) Amplification of gene of interest using Polymerase Chain Reaction (PCR) is a reaction in which multiple copies of specific DNA (gene of interest) sequence are made (amplification) in-vitro.
(v) Ligation of DNA fragment into a vector requires a vector DNA and source DNA.
(a) These are cut with endonuclease to obtain sticky ends.
(b) Both are then ligated by mixing vector DNA, gene of interest and enzyme DNA ligase to form recombinant DNA.
(vi) Insertion of recombinant DNA into the host cell/organism occurs by several methods, before which the recipient cells are made competent to receive the DNA.
(a) If recombinant DNA carrying antibiotic resistance gene (e.g. ampicillin), is transferred into E. coli cells, the host cell is transformed
into ampicillin resistant cell.
(b) The ampicillin resistant gene can be called a selectable marker.
(c) When transformed cells are grown on agar plates containing ampicillin, only transformants will grow and others will dic.
(vii) Culturing the host cells The cell containing the foreign gene is cultured on an appropriate medium at optimal conditions. The DNA gets multiplied.
(viii) Extraction of desired gene product is carried out in the following steps
(a) A protein encoding gene expressed in a heterologous host is called recombinant protein.
(b) Cells having genes of interest can be grown on a small or on a large scale.