Literature DB >> 2826389

Rhizobium japonicum USDA 191 has two nodD genes that differ in primary structure and function.

E R Appelbaum1, D V Thompson, K Idler, N Chartrain.   

Abstract

Several Rhizobium genes (designated nod genes) are involved in early steps in nodule formation. Here we present the results of DNA sequence and functional analysis of two nodD genes from the symbiotic plasmid of USDA 191, a fast-growing strain that forms nitrogen-fixing nodules on soybeans. Both genes encoded full-length nodD-related polypeptides, which were 69% homologous to each other. One of these genes, nodD1, complemented a Rhizobium trifolii nodD::Tn5 mutant for clover nodulation; the other gene, nodD2, did not. The nodD1 coding region was preceded by a conserved DNA sequence previously noted in other rhizobia, but no such sequence was found in front of nodD2. Plants inoculated with a nodD1 insertion mutant appeared to be nitrogen starved and had a greatly reduced nodule number. Plants inoculated with a nodD2 mutant had a partially nitrogen-starved appearance and normal nodule number, were slightly delayed in nodule formation, and formed nodules that contained reduced levels of nodulin-35 and had fewer bacteroids per infected plant cell. Thus, both of these genes are involved in symbiosis. USDA 191 carrying extra copies of nodD2 on a plasmid vector had an altered colony morphology that suggested inhibition of exopolysaccharide synthesis. The predicted gene products of nodD1 and nodD2 both showed homology to LysR, an E. coli regulatory protein. We conclude that nodD1 probably has the same function as nodD in temperate rhizobia, namely, activation of nodABC transcription in the presence of plant signals. nodD2 may be involved in regulation of exopolysaccharide synthetic genes.

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Year:  1988        PMID: 2826389      PMCID: PMC210599          DOI: 10.1128/jb.170.1.12-20.1988

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  36 in total

1.  Phaseolin gene from bean is expressed after transfer to sunflower via tumor-inducing plasmid vectors.

Authors:  N Murai; J D Kemp; D W Sutton; M G Murray; J L Slightom; D J Merlo; N A Reichert; C Sengupta-Gopalan; C A Stock; R F Barker; T C Hall
Journal:  Science       Date:  1983-11-04       Impact factor: 47.728

2.  Expression of symbiotic genes of Rhizobium japonicum USDA 191 in other rhizobia.

Authors:  E R Appelbaum; T J McLoughlin; M O'Connell; N Chartrain
Journal:  J Bacteriol       Date:  1985-07       Impact factor: 3.490

3.  Induction of the nodA promoter of Rhizobium leguminosarum Sym plasmid pRL1JI by plant flavanones and flavones.

Authors:  S A Zaat; C A Wijffelman; H P Spaink; A A van Brussel; R J Okker; B J Lugtenberg
Journal:  J Bacteriol       Date:  1987-01       Impact factor: 3.490

4.  Exopolysaccharide-deficient mutants of Rhizobium meliloti that form ineffective nodules.

Authors:  J A Leigh; E R Signer; G C Walker
Journal:  Proc Natl Acad Sci U S A       Date:  1985-09       Impact factor: 11.205

5.  Nodule initiation elicited by noninfective mutants of Rhizobium phaseoli.

Authors:  K A Vandenbosch; K D Noel; Y Kaneko; E H Newcomb
Journal:  J Bacteriol       Date:  1985-06       Impact factor: 3.490

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.  At least two nodD genes are necessary for efficient nodulation of alfalfa by Rhizobium meliloti.

Authors:  M Göttfert; B Horvath; E Kondorosi; P Putnoky; F Rodriguez-Quiñones; A Kondorosi
Journal:  J Mol Biol       Date:  1986-10-05       Impact factor: 5.469

8.  DNA sequence of the Rhizobium leguminosarum nodulation genes nodAB and C required for root hair curling.

Authors:  L Rossen; A W Johnston; J A Downie
Journal:  Nucleic Acids Res       Date:  1984-12-21       Impact factor: 16.971

9.  Nodulin-35: a subunit of specific uricase (uricase II) induced and localized in the uninfected cells of soybean nodules.

Authors:  H Bergmann; E Preddie; D P Verma
Journal:  EMBO J       Date:  1983       Impact factor: 11.598

10.  The nodD gene of Rhizobium leguminosarum is autoregulatory and in the presence of plant exudate induces the nodA,B,C genes.

Authors:  L Rossen; C A Shearman; A W Johnston; J A Downie
Journal:  EMBO J       Date:  1985-12-16       Impact factor: 11.598

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  23 in total

Review 1.  Regulation of nodulation gene expression by NodD in rhizobia.

Authors:  H R Schlaman; R J Okker; B J Lugtenberg
Journal:  J Bacteriol       Date:  1992-08       Impact factor: 3.490

2.  Homology of the ligand-binding regions of Rhizobium symbiotic regulatory protein NodD and vertebrate nuclear receptors.

Authors:  Z Györgypal; A Kondorosi
Journal:  Mol Gen Genet       Date:  1991-04

3.  Relationship of the Presence and Copy Number of Plasmids to Exopolysaccharide Production and Symbiotic Effectiveness in Rhizobium fredii USDA 206.

Authors:  W M Barbour; G H Elkan
Journal:  Appl Environ Microbiol       Date:  1989-04       Impact factor: 4.792

4.  Sequence of the Pseudomonas aeruginosa trpI activator gene and relatedness of trpI to other procaryotic regulatory genes.

Authors:  M Chang; A Hadero; I P Crawford
Journal:  J Bacteriol       Date:  1989-01       Impact factor: 3.490

5.  A large family of bacterial activator proteins.

Authors:  S Henikoff; G W Haughn; J M Calvo; J C Wallace
Journal:  Proc Natl Acad Sci U S A       Date:  1988-09       Impact factor: 11.205

Review 6.  The Rhizobium-plant symbiosis.

Authors:  P van Rhijn; J Vanderleyden
Journal:  Microbiol Rev       Date:  1995-03

7.  Evidence that the transcription activator encoded by the Pseudomonas putida nahR gene is evolutionarily related to the transcription activators encoded by the Rhizobium nodD genes.

Authors:  M A Schell; M Sukordhaman
Journal:  J Bacteriol       Date:  1989-04       Impact factor: 3.490

8.  Infection of soybean and pea nodules by Rhizobium spp. purine auxotrophs in the presence of 5-aminoimidazole-4-carboxamide riboside.

Authors:  J D Newman; R J Diebold; B W Schultz; K D Noel
Journal:  J Bacteriol       Date:  1994-06       Impact factor: 3.490

9.  Expression of Rhizobium leguminosarum CFN42 genes for lipopolysaccharide in strains derived from different R. leguminosarum soil isolates.

Authors:  B A Brink; J Miller; R W Carlson; K D Noel
Journal:  J Bacteriol       Date:  1990-02       Impact factor: 3.490

10.  Phenotype conversion in Pseudomonas solanacearum due to spontaneous inactivation of PhcA, a putative LysR transcriptional regulator.

Authors:  S M Brumbley; B F Carney; T P Denny
Journal:  J Bacteriol       Date:  1993-09       Impact factor: 3.490

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