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Q.The organism used in construction of the first artificial recombinant DNA by Cohen and Boyer in 1972 was :

(a) E. coli
(b) Salmonella typhimurium
(c) Agrobacterium tumefaciens
(d) Bacillus thuringiensis
CBSECBSE Class XII Board 2023MCQ· 1mImportance★★★★★
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The first artificial recombinant DNA was constructed using the bacterium Salmonella typhimurium as the source of the plasmid, not E. coli.

The year 1972 marks a watershed moment in biology. Stanley Cohen and Herbert Boyer performed the experiment that gave birth to genetic engineering. They took a plasmid from one bacterium, cut it, inserted a piece of foreign DNA, and then put this hybrid molecule back into a living cell. The result was the first artificial recombinant DNA — a molecule that combined genetic material from two different sources.

The key to their success was choosing the right raw materials. For the plasmid — the circular DNA that would serve as the vector — they did not use the common lab workhorse E. coli. Instead, they turned to a different bacterium: Salmonella typhimurium. This species carried a plasmid that had a single recognition site for the restriction enzyme EcoRI, making it ideal for cutting and inserting a foreign gene. The foreign DNA they inserted came from a different Salmonella species, and the entire construct was then introduced into E. coli cells, which replicated the recombinant plasmid.

Note

The textbook (NCERT Class 12 Biology, Chapter 11: Biotechnology: Principles and Processes) explicitly states that Cohen and Boyer used the plasmid from Salmonella typhimurium for this landmark experiment. The common misconception that E. coli was the source of the first recombinant plasmid arises because E. coli was the host cell that ultimately carried and multiplied the recombinant DNA.

Why does this detail matter? Because it highlights a core principle of genetic engineering: the vector (the carrier DNA) and the host (the cell that replicates it) are often different organisms. The plasmid from Salmonella typhimurium had the right properties — a single EcoRI site, the ability to replicate independently, and a selectable marker (antibiotic resistance) — that made it the perfect tool for this first proof-of-concept. …

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