Monday, September 4, 2017

Mutation and Genetic Engineering

Exposing organisms to agents such as mustard chemicals, ultraviolet light, and x-rays increases mutation rate by damaging chromosomes. In strain development through mutagenesis, the idea is to limit the mutagen exposure to kill about 99 percent of the organisms. The few survivors of this intense treatment are usually mutants. Most of the mutations are harmful to the cell, but a very small number may have economic importance in that impaired cellular control may result in better yields of product. The key is to have a procedure for selecting out the useful mutants. Screening of many strains to find the very few worthy of further study is tedious and expensive. Such screening that was so very important to biotechnology a few decades ago is becoming obsolete because of genetic improvements based on recombinant DNA technology.

Whereas mutagenic agents delete or scramble genes, recombinant DNA techniques add desirable genetic material from very different cells. The genes may come from plant, animal, or microbial cells, or in a few instances they may be synthesized in the laboratory from known nucleic acid sequences in natural genes. Opening a chromosome and splicing in foreign DNA is simple in concept, but there are complications.

Genes in fragments of DNA must have control signals from other nucleic acid sequences in order to function. Both the gene and its controls must be spliced into the chromosomes of the receiving culture.

Bacterial chromosomes (circular DNA molecules) are cut open with enzymes, mixed with the new fragments to be incorporated, and closed enzymatically. The organism will acquire new traits. This technique is referred to as recombinant technology.

There are many tricks and some art in genetic engineering. Examples would be using bacteriophage infection to introduce a gene for producing a new enzyme in a cell. Certain strains of E. coli, B. subtilis, yeast, and streptomyces are the usual working organisms (cloning vectors) to which genes are added. The reason for this is that the genetics of these organisms is well understood and the methodology has become fairly routine.

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1 comment:

Neo said...

Hey! Thank you so much for making things so simple and easily understandable... :)