Recombinant DNA and the Birth of BiotechRecombinant DNA in the Lab
In a series of experiments, between 1972 and 1974, Stanley Cohen, Herbert Boyer, and their colleagues, at Stanford University and the University of California, San Francisco built on the work of recombinant DNA pioneers such as Paul Berg to develop techniques that would form the basis of recombinant DNA technology. These experiments helped spur the birth of the biotechnology industry.
Since 1959, scientists knew that bacteria contain extra loops of DNA called “plasmids” in addition to their chromosome. In nature, bacteria can swap these plasmids with one another, quickly transferring beneficial genes like those that code for antibiotic resistance. By the early 1970s, investigators had isolated several plasmids as well as special enzymes known as “restriction endonucleases” that work like scissors to cut open the loops of plasmids.
Herbert Boyer had expertise with restriction endonucleases and Stanley Cohen studied plasmids, and after meeting at a conference in 1972, the two decided to combine their research efforts. After preliminary experiments in 1973, the Cohen-Boyer team was able to cut open a plasmid loop from one species of bacteria, insert a gene from different bacterial species and close the plasmid. This created a recombinant DNA molecule-- a plasmid containing recombined DNA from two different sources. Next, they inserted the plasmid into bacteria and demonstrated that the recombinant DNA could be used by bacteria. The team had created the first genetically modified organisms.
|Stanley Cohen’s laboratory installed in NMAH’s exhibit Science in American Life, which ran from 1994-2012. Credit:Flickr user Ryan Somma|
A year later, they would use this technique to insert a gene from a frog into bacteria, proving that it was possible to transfer genes between two very different organisms. The technology for creating these “molecular chimeras” was patented on December 2, 1980 (US Patent 4,237,224.) Below are a number of objects used in the Cohen lab during the recombinant DNA experiments.
"Recombinant DNA and the Birth of Biotech - Recombinant DNA in the Lab" showing 1 items.
- Description (Brief)
- This case held electron microscope (EM) grids used in the lab of Stanley Cohen at Stanford University. Made from tiny circles of copper mesh, EM grids are analogous to the glass slides used to mount samples for viewing under a light microscope. These grids were used to support recombinant bacteria and recombinant plasmids for study and analysis under the electron microscope. One of the grids contains a sample of Cohen and Boyer’s first recombinant plasmid. Photographic images of the first recombinant plasmids used in publications on Cohen and Boyer’s research were made from these grids.
- For more information on the Cohen/Boyer experiments with recombinant DNA, see object 1987.0757.01
- Accession File
- “EM Grid Preparation.” Purdue University. Accessed December 2012. http://bilbo.bio.purdue.edu/~baker/documentation/sample_and_prep/b2.htm
- Currently not on view
- Cohen, Stanley N.
- ID Number
- catalog number
- accession number
- Data Source
- National Museum of American History, Kenneth E. Behring Center