AEM
Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Thompson, J. K.
Right arrow Articles by Collins, M. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Thompson, J. K.
Right arrow Articles by Collins, M. A.
Agricola
Right arrow Articles by Thompson, J. K.
Right arrow Articles by Collins, M. A.

 Previous Article  |  Next Article 

Applied and Environmental Microbiology, May 1999, p. 1910-1914, Vol. 65, No. 5
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

Potential of Conjugal Transfer as a Strategy for the Introduction of Recombinant Genetic Material into Strains of Lactobacillus helveticus

J. K. Thompson,1,* K. J. McConville,1 C. McReynolds,1 and M. A. Collins1,2

Department of Food Science (Food Microbiology), Department of Agriculture for Northern Ireland,1 and the Queen's University of Belfast,2 Belfast BT9 5PX, Northern Ireland, United Kingdom

Received 8 July 1998/Accepted 9 February 1999

Cointegrates generated between a plasmid pIP501 deletion derivative (pVA797) and nonconjugative shuttle vector pSA3 were confirmed as capable of exconjugation from lactococci into a range of strains of Lactobacillus helveticus with the concomitant expression of a recombinant gene. The plasmid cointegrate that was formed appeared to be segregationally stable at 37°C in some host strains. In all strains, however, the plasmid became increasingly unstable as the incubation temperature was raised. The technique offers not only a generalized method for the introduction of novel genetic material into this important industrial microbe but also the possibility of exploiting the thermal sensitivity of the plasmid to enable it to act as a delivery system for the integration of cloned genes into the bacterial chromosome, at restrictive temperatures, by recombination at regions of homology.


* Corresponding author. Mailing address: Department of Food Science (Food Microbiology), Department of Agriculture for Northern Ireland, Newforge Ln., Belfast BT9 5PX, Northern Ireland, United Kingdom. Phone: 44.1232.255616. Fax: 44.1232.668376. E-mail: keith.thompson{at}dani.gov.uk.


Applied and Environmental Microbiology, May 1999, p. 1910-1914, Vol. 65, No. 5
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
J. Bacteriol. Microbiol. Mol. Biol. Rev. Eukaryot. Cell All ASM Journals

Copyright © 1999 by the American Society for Microbiology. All rights reserved.