Recombinant DNA Technology

Recombinant DNA Technology - joining of DNA molecules from two different species that are
inserted into a host organism to produce new

Recombinant DNA (rDNA), - the general name for a piece of DNA that has been created by the
combination of at least two different DNA strands.
They are DNA molecules formed by laboratory methods of genetic recombination to bring together
genetic material from multiple sources, creating sequences that would not otherwise be found in the
genome.
Steps of Genetic Recombination Technology
1. Isolation of Genetic Material - it must be separated and purified which involves enzymes such as
restriction enzymes.
2. Restriction Enzymes Digestion - The technique ‘Agarose Gel Electrophoresis’
Reveals the progress of the restriction enzyme digestion.
‘Agarose Gel Electrophoresis’ - This technique involves running out the DNA on an agarose gel.
On the application of current, the negatively charged DNA travels to the positive electrode and is
separated out based on size. This allows separating and cutting out the digested DNA fragments. The
vector DNA is also processed using the same procedure.
3. Amplification Using PCR - Polymerase Chain Reaction or PCR is a method of
making multiple copies of a DNA sequence using the enzyme – DNA polymerase
in vitro.
It helps to amplify a single copy or a few copies of DNA into thousands
to millions of copies.
PCR reactions are run on thermal cyclers using the following components:
a.)Template – DNA to be amplified
b.)Primers – small, chemically synthesized oligonucleotides that are complementary to a region of
the DNA.
c.) Enzyme – DNA polymerase
d.)Nucleotides – needed to extend the primers by the enzyme.
e.) The cut fragments of DNA can be amplified using PCR and then ligated with the cut vector.
4. Ligation of DNA Molecules – The purified DNA and the vector of interest are cut with the same
restriction enzyme. This gives us the cut fragment of DNA andt he cut vector that is now open. The
process of joining these two pieces together using the enzyme DNA ligase is ligation. The
resulting DNA molecule is a hybridof two DNA molecules – the interest molecule and the vector. In
the terminologyof genetics this intermixing of different DNA strands is called recombination.
Hence, this new hybrid DNA molecule is also called a recombinant DNA molecule and the
technology is referred to as the recombinant DNA technology
.5. Insertion of Recombinant DNA into Host - In this step, the recombinant DNA is introduced into a
recipient host cell mostly, a bacterial cell. This process is called transformation. Bacterial cells do not
accept foreign DNA easily. Therefore, they are treated to make them competent to accept new DNA.
The processes used may be thermal shock, Ca++ ion treatment, and electroporation.
6. Isolation of Recombinant Cells-The transformation process generates a mixed population of

transformed and non-transformed host cells. The selection process involves filtering the
transformed host cells only. For isolation of recombinant cells from non-recombinant cells, a marker
gene of the plasmid vector is employed.
7. Obtaining or culturing the Foreign Gene product - When you insert a piece of alien DNA into a
cloning vector and transfer it into a bacterial cell, the alien DNA gets multiplied. The ultimate aim is
to produce a desirable protein expression. The cells harboring cloned genes of interest are grown on
a small scale in the laboratory. These cell cultures are used for extracting the desired protein using
various separation techniques.
Importance of Recombinant DNA Technology

Recombinant DNA technology is playing a vital role in improving health conditions by developing
new vaccines and pharmaceuticals. The treatment strategies are also improved by developing
diagnostic kits, monitoring devices, and new therapeutic approaches. Synthesis of synthetic human
insulin and erythropoietin by genetically modified bacteria and the production of new types of
experimental mutant mice for research purposes are some one of the leading examples of genetic
engineering in health. Likewise, genetic engineering strategies have been employed to tackle
environmental issues such as converting wastes into biofuels and bioethanol, cleaning the oil spills,
carbon, and other toxic wastes, and detecting arsenic and other contaminants in drinking water. The
genetically modified microbes are also effectively used in biomining and bioremediation.

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Recombinant DNA Technology

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Recombinant DNA Technology - joining of DNA molecules from two different species that are

inserted into a host organism to produce new

6. Isolation of Recombinant Cells-The transformation process generates a mixed population of

Importance of Recombinant DNA Technology

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