Transgenic bacteria contain foreign gene that is intentionally introduced into its genome. They are manipulated to express the desirable gene for the production of various commercially important products.
An example of transgenic bacteria is E.coli. In the plasmid of E.coli, the two DNA sequences corresponding to A and B chain of human insulin are inserted, so as to produce the respective human insulin chains. Hence, after the insertion of insulin gene into the bacterium, it becomes transgenic and starts producing chains of human insulin. Later on, these chains are extracted from E.coli and combined to form human insulin.
Transgenic bacteria, genetically modified with genes sourced from other organisms, are employed for large-scale production of desired gene products.
For example, after extracting the human insulin gene from the human genome and creating recombinant DNA (rDNA) containing this gene, the rDNA, consisting of vector DNA and the insulin gene, is inserted into E. coli bacteria. These modified bacterial cells, known as transgenic bacteria, are then utilized to produce insulin protein on a large scale.
The following diagram shown restriction sites in E. coli cloning vector pBR322. Find the role of ‘X’ and ‘Y’gens :
Annealing process of PCR is performed at \(\_\_\_\) temperature.
The correct IUPAC name of \([ \text{Pt}(\text{NH}_3)_2\text{Cl}_2 ]^{2+} \) is:
Biotechnology is the technology that utilizes biological systems, living organisms, or parts of this to develop or create different products.
For example, brewing and baking bread fall within the concept of biotechnology (use of yeast (= living organism) to produce the desired product).
Alternative to conventional farming: A possible solution is the use of genetically modified crops which is an alternative path to conventional farming.
In the area of healthcare, recombinant DNA technological processes have made an immense impact which enables the mass production of safe and more effective therapeutic drugs.
A collection of methods that allows the correction of a gene defect that has been diagnosed in a child/embryo is called Gene Therapy.
For editing genomes, CRISPR is a simple yet powerful tool which allows researchers to easily alter DNA sequences and modify gene function.