Literature DB >> 8986807

The common nodABC genes of Rhizobium meliloti are host-range determinants.

P Roche1, F Maillet, C Plazanet, F Debellé, M Ferro, G Truchet, J C Promé, J Dénarié.   

Abstract

Symbiotic bacteria of the genus Rhizobium synthesize lipo-chitooligosaccharides, called Nod factors (NFs), which act as morphogenic signal molecules on legume hosts. The common nodABC genes, present in all Rhizobium species, are required for the synthesis of the core structure of NFs. NodC is an N-acetylglucosaminyltransferase, and NodB is a chitooligosaccharide deacetylase; NodA is involved in N-acylation of the aminosugar backbone. Specific nod genes are involved in diverse NF substitutions that confer plant specificity. We transferred to R. tropici, a broad host-range tropical symbiont, the ability to nodulate alfalfa, by introducing nod genes of R. meliloti. In addition to the specific nodL and nodFE genes, the common nodABC genes of R. meliloti were required for infection and nodulation of alfalfa. Purified NFs of the R. tropici hybrid strain, which contained chitin tetramers and were partly N-acylated with unsaturated C16 fatty acids, were able to elicit nodule formation on alfalfa. Inactivation of the R. meliloti nodABC genes suppressed the ability of the NFs to nodulate alfalfa. Studies of NFs from nodA, nodB, nodC, and nodI mutants indicate that (i) NodA of R. meliloti, in contrast to NodA of R. tropici, is able to transfer unsaturated C16 fatty acids onto the chitin backbone and (ii) NodC of R. meliloti specifies the synthesis of chitin tetramers. These results show that allelic variation of the common nodABC genes is a genetic mechanism that plays an important role in signaling variation and in the control of host range.

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Year:  1996        PMID: 8986807      PMCID: PMC26400          DOI: 10.1073/pnas.93.26.15305

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  33 in total

Review 1.  Signaling and host range variation in nodulation.

Authors:  J Dénarié; F Debellé; C Rosenberg
Journal:  Annu Rev Microbiol       Date:  1992       Impact factor: 15.500

2.  The NodA proteins of Rhizobium meliloti and Rhizobium tropici specify the N-acylation of Nod factors by different fatty acids.

Authors:  F Debellé; C Plazanet; P Roche; C Pujol; A Savagnac; C Rosenberg; J C Promé; J Dénarié
Journal:  Mol Microbiol       Date:  1996-10       Impact factor: 3.501

3.  Identification of a Rhizobium meliloti pSym2011 region controlling the host specificity of root hair curling and nodulation.

Authors:  G Truchet; F Debellé; J Vasse; B Terzaghi; A M Garnerone; C Rosenberg; J Batut; F Maillet; J Dénarié
Journal:  J Bacteriol       Date:  1985-12       Impact factor: 3.490

4.  In vitro sulfotransferase activity of Rhizobium meliloti NodH protein: lipochitooligosaccharide nodulation signals are sulfated after synthesis of the core structure.

Authors:  M Schultze; C Staehelin; H Röhrig; M John; J Schmidt; E Kondorosi; J Schell; A Kondorosi
Journal:  Proc Natl Acad Sci U S A       Date:  1995-03-28       Impact factor: 11.205

5.  Structural identification of metabolites produced by the NodB and NodC proteins of Rhizobium leguminosarum.

Authors:  H P Spaink; A H Wijfjes; K M van der Drift; J Haverkamp; J E Thomas-Oates; B J Lugtenberg
Journal:  Mol Microbiol       Date:  1994-09       Impact factor: 3.501

6.  Broad host range DNA cloning system for gram-negative bacteria: construction of a gene bank of Rhizobium meliloti.

Authors:  G Ditta; S Stanfield; D Corbin; D R Helinski
Journal:  Proc Natl Acad Sci U S A       Date:  1980-12       Impact factor: 11.205

7.  The NodC protein of Azorhizobium caulinodans is an N-acetylglucosaminyltransferase.

Authors:  R A Geremia; P Mergaert; D Geelen; M Van Montagu; M Holsters
Journal:  Proc Natl Acad Sci U S A       Date:  1994-03-29       Impact factor: 11.205

8.  Genes controlling early and late functions in symbiosis are located on a megaplasmid in Rhizobium meliloti.

Authors:  C Rosenberg; P Boistard; J Dénarié; F Casse-Delbart
Journal:  Mol Gen Genet       Date:  1981

9.  Biosynthesis of Rhizobium meliloti lipooligosaccharide Nod factors: NodA is required for an N-acyltransferase activity.

Authors:  E M Atkinson; M M Palcic; O Hindsgaul; S R Long
Journal:  Proc Natl Acad Sci U S A       Date:  1994-08-30       Impact factor: 11.205

10.  Host-specific regulation of nodulation genes in Rhizobium is mediated by a plant-signal, interacting with the nodD gene product.

Authors:  B Horvath; C W Bachem; J Schell; A Kondorosi
Journal:  EMBO J       Date:  1987-04       Impact factor: 11.598

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  28 in total

Review 1.  Nodulation gene regulation in Bradyrhizobium japonicum: a unique integration of global regulatory circuits.

Authors:  John Loh; Gary Stacey
Journal:  Appl Environ Microbiol       Date:  2003-01       Impact factor: 4.792

2.  A Medicago truncatula tobacco retrotransposon insertion mutant collection with defects in nodule development and symbiotic nitrogen fixation.

Authors:  Catalina I Pislariu; Jeremy D Murray; JiangQi Wen; Viviane Cosson; RajaSekhara Reddy Duvvuru Muni; Mingyi Wang; Vagner A Benedito; Andry Andriankaja; Xiaofei Cheng; Ivone Torres Jerez; Samuel Mondy; Shulan Zhang; Mark E Taylor; Million Tadege; Pascal Ratet; Kirankumar S Mysore; Rujin Chen; Michael K Udvardi
Journal:  Plant Physiol       Date:  2012-06-07       Impact factor: 8.340

3.  Nitrogen-fixing symbiosis between photosynthetic bacteria and legumes.

Authors:  Eric Giraud; Darrell Fleischman
Journal:  Photosynth Res       Date:  2004       Impact factor: 3.573

Review 4.  Molecular basis of symbiotic promiscuity.

Authors:  X Perret; C Staehelin; W J Broughton
Journal:  Microbiol Mol Biol Rev       Date:  2000-03       Impact factor: 11.056

5.  Ribosomal protein gene cluster analysis in eubacterium genomics: homology between Sinorhizobium meliloti strain 1021 and Bacillus subtilis.

Authors:  F Barloy-Hubler; V Lelaure; F Galibert
Journal:  Nucleic Acids Res       Date:  2001-07-01       Impact factor: 16.971

6.  Associations among rhizobial chromosomal background, nod genes, and host plants based on the analysis of symbiosis of indigenous rhizobia and wild legumes native to Xinjiang.

Authors:  Tian Xu Han; Chang Fu Tian; En Tao Wang; Wen Xin Chen
Journal:  Microb Ecol       Date:  2010-02       Impact factor: 4.552

7.  Three phylogenetic groups of nodA and nifH genes in Sinorhizobium and Mesorhizobium isolates from leguminous trees growing in Africa and Latin America.

Authors:  K Haukka; K Lindström; J P Young
Journal:  Appl Environ Microbiol       Date:  1998-02       Impact factor: 4.792

8.  Identification of essential amino acids in the Azorhizobium caulinodans fucosyltransferase NodZ.

Authors:  V Chazalet; K Uehara; R A Geremia; C Breton
Journal:  J Bacteriol       Date:  2001-12       Impact factor: 3.490

9.  Structural basis for regulation of rhizobial nodulation and symbiosis gene expression by the regulatory protein NolR.

Authors:  Soon Goo Lee; Hari B Krishnan; Joseph M Jez
Journal:  Proc Natl Acad Sci U S A       Date:  2014-04-14       Impact factor: 11.205

Review 10.  Emergence of β-rhizobia as new root nodulating bacteria in legumes and current status of the legume-rhizobium host specificity dogma.

Authors:  Ahmed Idris Hassen; Sandra C Lamprecht; Francina L Bopape
Journal:  World J Microbiol Biotechnol       Date:  2020-02-24       Impact factor: 3.312

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