Development of improved versatile broad-host-range vectors for use in methylotrophs and other Gram-negative bacteria The GenBank accession numbers for the sequences reported in this paper are AF327711, AF327712, AF327713, AF327714, AF327715, AF327716, AF327717, AF327718, AF327719 and AF327720.
Top Cited Papers
- 1 August 2001
- journal article
- Published by Microbiology Society in Microbiology
- Vol. 147 (8), 2065-2075
- https://doi.org/10.1099/00221287-147-8-2065
Abstract
Full exploitation of the information available in bacterial genome sequences requires the availability of facile tools for rapid genetic manipulation. One bacterium for which new genetic tools are needed is the methylotroph Methylobacterium extorquens AM1. IncQ and small IncP vectors were shown to be unsuitable for use in this bacterium, but a spontaneous mutant of a small IncP plasmid was isolated that functioned efficiently in M. extorquens AM1. This plasmid was sequenced and used as a base for developing improved broad-host-range cloning vectors. These vectors were found to replicate in a wide variety of bacterial species and have the following advantages: (1) high copy number in Escherichia coli; (2) small size (7·2 and 8·0 kb); (3) complete sequences; (4) variety of unique restriction sites; (5) blue–white screening via lacZα; (6) conjugative mobilization between bacterial species; and (7) readily adaptable into species-specific promoter-probe and expression vectors. Two low-background promoter-probe vectors were constructed based on these cloning vectors with either lacZ or xylE as reporter genes; these were shown to report gene expression effectively in M. extorquens AM1. Specific expression vectors were developed for use in M. extorquens AM1, which were shown to express foreign genes at significant levels, and a simple strategy is outlined to develop specific expression vectors for other bacteria. The strong mxaF promoter was used for expression, since E. coli lac-derived promoters were expressed at very low levels. This suite of genetic tools will enable a more sophisticated analysis of the physiology of M. extorquens AM1, and these vectors should also be valuable tools in the study of a variety of bacterial species.Keywords
This publication has 35 references indexed in Scilit:
- A vector for systematic gene inactivation in Bacillus subtilisMicrobiology, 1998
- Construction of insertion and deletion mxa mutants of Methylobacterium extorquens AM1 by electroporationFEMS Microbiology Letters, 1998
- Sequence and characterization ofmxaB, a response regulator involved in regulation of methanol oxidation, and ofmxaW, a methanol-regulated gene inMethylobacterium extorquensAM1FEMS Microbiology Letters, 1998
- Four new derivatives of the broad-host-range cloning vector pBBR1MCS, carrying different antibiotic-resistance cassettesGene, 1995
- Complete Nucleotide Sequence of Birmingham IncPα PlasmidsJournal of Molecular Biology, 1994
- Identification of methanol-regulated promoter sequences from the facultative methylotrophic bacterium Methylobacterium organophilum XXJournal of General Microbiology, 1993
- The Aeromonas hydrophila exeE gene, required both for protein secretion and normal outer membrane biogenesis, is a member of a general secretion pathwayMolecular Microbiology, 1992
- Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mpl8 and pUC19 vectorsGene, 1985
- Suppression of cole1 replication properties by the Inc P-1 plasmid RK2 in hybrid plasmids constructed in vitroJournal of Molecular Biology, 1979
- Methanol Assimilation by Hyphomicrobium sp.Journal of General Microbiology, 1973