Abstract
THE discovery of recombination in Escherichia coli1,2 has given to bacterial genetics a much wider scope than it had before. Three years after its first publication, however, the results obtained by Leder-berg with the strain known as K 12 still stand alone, no other bacterial strain having been found to show a similar behaviour. This is partly due to the fact that demonstration of recombination is a slow business, owing to the work required for the preparation of suitable substrains. In fact, the only method known so far is still the original one of mixing substrains having different growth requirements on a minimal medium where neither parental strain can grow, but on which cells possessing some of the synthetic capacities of one strain and some of the other will be able to form colonies. As such colonies, called by Lederberg 'prototrophs', usually appear at a very low rate, care must be taken that recombination is not simulated by back-mutation in either parental strain.
This is a preview of subscription content, access via your institution
Access options
Subscribe to this journal
Receive 51 print issues and online access
$199.00 per year
only $3.90 per issue
Buy this article
- Purchase on Springer Link
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
Similar content being viewed by others
References
Lederberg, J., and Tatum, E. L., Nature, 158, 558 (1946).
Lederberg, J., Genetics, 32, 505 (1947).
Cavalli, L. L., 100th Meeting of the Genetical Society, Cambridge, 1949.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
CAVALLI, L., HESLOT, H. Recombination in Bacteria: Outcrossing Escherichia coli K 12. Nature 164, 1057–1058 (1949). https://doi.org/10.1038/1641057c0
Issue Date:
DOI: https://doi.org/10.1038/1641057c0
This article is cited by
Comments
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.