The symbiotic defect of Rhizobium meliloti exopolysaccharide mutants is suppressed by lpsZ+, a gene involved in lipopolysaccharide biosynthesis
- 1 May 1990
- journal article
- research article
- Published by American Society for Microbiology in Journal of Bacteriology
- Vol. 172 (5) , 2622-2632
- https://doi.org/10.1128/jb.172.5.2622-2632.1990
Abstract
Exo mutants of Rhizobium meliloti SU47, which fail to secrete acidic extracellular polysaccharide (EPS), induce Fix- nodules on alfalfa. However, mutants of R. meliloti Rm41 carrying the same exo lesions induce normal Fix+ nodules. We show that such induction is due to a gene from strain Rm41, which we call lpsZ+, that is missing in strain SU47. lpsZ+ does not restore EPS production but instead alters the composition and structure of lipopolysaccharide. In both SU47 and Rm41, either lpsZ+ or exo+ is sufficient for normal nodulation. This suggests that in R. meliloti EPS and lipopolysaccharide can perform the same function in nodule development. ImagesThis publication has 48 references indexed in Scilit:
- A novel exopolysaccharide can function in place of the Calcofluor-binding exopolysaccharide in nodulation of alfalfa by Rhizobium melilotiCell, 1989
- Rhizobium meliloti mutants that fail to succinylate their Calcofluor-binding exopolysaccharide are defective in nodule invasionCell, 1987
- Plasmids related to the broad host range vector, pRK290, useful for gene cloning and for monitoring gene expressionPlasmid, 1985
- Rhizobium meliloti carries two megaplasmidsPlasmid, 1985
- Cloning of Rhizobium meliloti nodulation genes by direct complementation of Nod− mutantsNature, 1982
- Structural elucidation, using h.p.l.c.-m.s. and g.l.c.-m.s., of the acidic polysaccharide secreted by rhizobium meliloti strain 1021Carbohydrate Research, 1981
- A general method for site-directed mutagenesis in prokaryotesNature, 1981
- Trimethoprim R Factors in Enterobacteria from Clinical SpecimensJournal of Medical Microbiology, 1974
- Bacteriophage ReceptorsAnnual Review of Microbiology, 1973
- A procedure for the isolation of deoxyribonucleic acid from micro-organismsJournal of Molecular Biology, 1961