Let's arrange the steps of recombinant DNA technology in the correct sequence:
(A) Isolation of desired DNA fragments: The first step involves isolating the specific DNA fragment that contains the gene of interest. This is done by using restriction enzymes to cut the DNA at specific locations.
(D) Ligation of DNA fragment into vector: The isolated DNA fragment is then inserted into a vector, such as a plasmid, using the process of ligation (using the enzyme ligase). This forms a recombinant DNA molecule.
(E) Transferring of recombinant DNA to host: The recombinant DNA is introduced into a host cell (like an E. coli bacterium) through methods like transformation, making it capable of replicating the recombinant DNA.
(B) Culturing the host cells: The host cells, now containing the recombinant DNA, are cultured in a suitable medium. This allows the host cells to multiply and replicate the recombinant DNA.
(C) Extraction of desired product: After culturing, the desired product (such as a protein) is extracted from the cultured cells, completing the process.
Thus, the correct sequence is:
(A) Isolation of desired DNA fragments, (D) Ligation of DNA fragment into vector, (E) Transferring of recombinant DNA to host, (B) Culturing the host cells, and (C) Extraction of desired product.
The correct answer is (2) (A), (D), (E), (B), (C).
The correct order is: (A) Isolation of desired DNA fragments, (D) Ligation of DNA fragment into vector, (E) Transferring recombinant DNA to host, (B) Culturing host cells, and (C) Extraction of the desired product. This sequence follows the typical recombinant DNA methodology.