"What do you understand by Recombinant DNA Technology?

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“What do you understand by Recombinant DNA Technology?

Discuss the Moral, Ethical, Social, Economic and Environmental Issues Associated with the Technology, giving your views.”

          The discovery of DNA is attributed to the research of three scientists in 1951; Francis Crick, Maurice Wilkins, and James Dewey Watson. They were all later accredited with the Nobel Prize in physiology and medicine in 1962. Thanks to their discovery science has been able to research and learn from DNA blueprints and use recombinant DNA technology to discover answers, vaccines and build immunity for many viruses. In recent years science has been using this new technology to genetically modify animals, plants and possibly the main aim being to modify the DNA of humans. Recombinant DNA technology or genetic engineering as it is more commonly known is a “method of changing the inherited characteristics of an organism in a predetermined way by altering its genetic material.” It involves “the combination of DNA from one organism with DNA from another organism.”

          Before the process of Recombinant DNA can begin there are two substances in bacterial cells that are required. The first is located in the cytoplasm of the bacterial cell, where there are small circular pieces of DNA known as plasmids these are used as vectors.  The second is the desired gene. There are three ways of isolating the gene; using DNA probes, working backwards from the protein or using messenger RNA. When the gene has been isolated it has to be cut from its DNA chain, this is done using Restriction Endonucleases (restriction enzymes).  These cut DNA molecules at specific sites. By choosing the correct restriction enzyme, DNA molecules from different organisms can be cut at predictable sites to extract specific genes from lengths of DNA. The desired gene is then spliced into a vector. A vector being a gene carrier is used to get the desired gene into the target organism.

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The desired gene and the plasmids are both cut using the same restriction enzyme so that they both have the same ‘sticky ends’.  The two ends are joined together, with the help of an enzyme called ligase. A new molecule is formed that contains genes from both the plasmid and another organism. This is recombinant DNA; this DNA formed is then introduced into the host cell and using antibiotics the cells containing the DNA are selected. The vectors then multiply and produce genetically identical daughter cells which also produce the desired protein. This is recombinant DNA; this DNA formed ...

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