The production of a large population of a DNA fragment in pure form is called as gene cloning.
It involves the formation of recombinant DNA and its introduction into the mother bacterial cell.
The recombinant DNA is formed by combining DNAs from two different organisms.
This process is called genetic engineering. A DNA fragment of one organism (called as Passenger DNA) is transferred into another organism by combining it with another DNA(called as Vehicle DNA).
Normally plasmid or bacteriophage DNA is used as Vehicle DNA. Both the passenger and vehicle DNA are cleaved by using restriction endonuclease enzyme and they are mixed under suitable conditions.
Their complementary sticky ends pair and their ends are sealed by ligase enzyme. The resulting DNA is called recombinant DNA.
The recombinant DNA is added to the culture containing growing host bacteria.
These bacteria take the recombinant DNA along with the nutrients.
This DNA replicates when the bacteria divide and produce a large clone of recombinant DNA.