Affiliation:
1. Department of Microbiology and Immunology, Dartmouth Medical School, Hanover, New Hampshire 03755
Abstract
ABSTRACT
A tool kit of vectors was designed to manipulate and express genes from a wide range of gram-negative species by using in vivo recombination.
Saccharomyces cerevisiae
can use its native recombination proteins to combine several amplicons in a single transformation step with high efficiency. We show that this technology is particularly useful for vector design. Shuttle, suicide, and expression vectors useful in a diverse group of bacteria are described and utilized. This report describes the use of these vectors to mutate
clpX
and
clpP
of the opportunistic pathogen
Pseudomonas aeruginosa
and to explore their roles in biofilm formation and surface motility. Complementation of the rhamnolipid biosynthetic gene
rhlB
is also described. Expression vectors are used for controlled expression of genes in two pseudomonad species. To demonstrate the facility of building complicated constructs with this technique, the recombination of four PCR-generated amplicons in a single step at >80% efficiency into one of these vectors is shown. These tools can be used for genetic studies of pseudomonads and many other gram-negative bacteria.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
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