BIOLOGY 3 Marks Question

Diagram of E.coli cloning vector pBR322 :

(a) In r-DNA technology, selectable markers are used to identify transformants and select successful transformants and they are helpful in eliminating nontransformants. These provide survival benefits to cells with exogenous DNA.
(b) The name of one such selectable marker considered useful for E. coli is—tetracycline, which is a gene that codes for resistance to antibiotics.
(c) It is called a beneficial selectable marker because it helps in identifying and selecting the transformant.

The main objective of almost all recombinant technologies is to produce the desired protein. For this, after cloning the desired gene and optimizing the conditions that induce the expression of the target protein, it is possible to produce them on a large scale. Cells harboring beneficial genes can be cultured in the laboratory on a small scale. The desired protein can be extracted from the culture and purified using various methods of separation. Cells can be multiplied in a continuous culture system, in which used medium is drained from one side and fresh medium is added from the other side so that the cells remain in their most functionally active log (exponential) phase. This culture method is useful for producing more biomass and producing more of the desired protein.
Bioreactors are used to produce these products in large quantities. Bioreactors are like vessels in which raw materials are converted into biologically specific products, individual enzymes etc. using microorganisms, plants, animals and human cells. The bioreactor provides optimum conditions to obtain the desired product. Temperature, pH, substrate, salts, vitamins, oxygen etc. are the optimum conditions for growth. Generally stirring type bioreactor is used the most.
Stirred tank bioreactors are cylindrical. Its curved base helps in mixing of the contents inside the bioreactor. The bioreactor has the availability of oxygen and a stirrer facility for mixing the mixture. Alternatively, air is sent into the bioreactor in the form of bubbles. The bioreactor is equipped with an agitator system, oxygen supply system, froth control system, pH control system, temperature control system and sampling ports from which a small amount of the culture can be taken out from time to time.

The technique in which recombinant DNA is obtained by introducing the DNA of one species into the DNA of another species is called genetic engineering.
In genetic engineering, recombinant DNA is created using gene cloning and gene transfer. The first recombinant DNA was created by adding an antibiotic-resistant transcription gene to the plasmid of Salmonella typhimarium. Stanley Cohen and Herbert Boyer’s work was accomplished in 1972 by cutting a piece of DNA from a plasmid, which contained the gene responsible for providing antibiotic resistance. The discovery of 'restriction enzymes' called molecular scissors made it possible to cut DNA at specific places. The cut DNA portion is combined with the plasmid DNA. This plasmid acts as a DNA vector which transfers the DNA attached to it. The work of connecting the antibiotic resistance gene with the vector is done by the enzyme DNA ligase, which works on the cut part of the DNA molecule and joins its ends. By this combination, new circular self-replicating DNA is formed in vitro, which is called recombinant DNA. When this DNA is transferred into Escherichia coli, it makes multiple copies by using the DNA polymerase enzyme of the new host. 

Taking a fragment of DNA from one organism and hybridizing it with the DNA of another organism is called recombinant DNA. In this technique, recombinant DNA is obtained by introducing the DNA of one species into the DNA of another species.
Microinjection : In this, DNA is injected under pressure into protoplasts or pollen grains or directly into the developing inflorescence.
Gene Gun : 1-3 micro mm diameter particles of gold or tungsten coated with DNA are fired into the target cells at high velocity by the bullet. Due to this, they penetrate the cell wall and enter inside the cell.

After gaining knowledge from bacteria and viruses, gene cloning was done in plants and animals also. Some types of bacteria and viruses were studied which are pathogens in plants and animals. For example, Agrobacterium tumifaciens is a pathogenic pathogen of many dicotyledonous plants. It transforms normal plant cells into tumors by transferring a segment of DNA called 'TDNA' and these tumor cells produce chemicals necessary for the pathogen. In the same way, retroviruses in animal cells transform normal cells into cancer cells. By understanding the art of gene transfer by pathogens in their eukaryote host, they can use this knowledge to transform these tools of pathogens into useful vectors for delivering genes of interest to humans. The Ti plasmid of Agrobacterium tumifaciens has now been adapted as a cloning vector that is not pathogenic to plants, but is used to transfer genes of interest to many plants. In the same  way, retrovirus is made harmless and used to modify desired genes in animal cells. In this way, when a gene or segment of DNA is attached to the appropriate vector, it is transferred to the bacterial, plant or animal host (where it continues to multiply).