Analysis of the Rhizobium meliloti exoH/exoK/exoL fragment: ExoK shows homology to excreted endo-beta-1,3-1,4-glucanases and ExoH resembles membrane proteins
BECKER A, KLEICKMANN A, Arnold W, Pühler A (1993)
Mol Gen Genet 238(1-2): 145-154.
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Einrichtung
Abstract / Bemerkung
Nucleotide sequencing of a 4.15 kb DNA fragment from megaplasmid 2 of Rhizobium meliloti 2011 revealed the location of the genes exoH, exoK and exoL. The putative proteins encoded by these genes have molecular weights of 41, 30, and 44 kDa, respectively. The hydrophobicity profile of the ExoH amino acid sequence resembles that of transmembrane proteins. The predicted exoL gene product does not contain hydrophobic regions, indicating a cytoplasmic localization. The exoK gene product is characterized by a putative signal peptide and exhibits significant homology to endo-beta-1,3-1,4-glucanases of bacilli and Clostridium thermocellum. R. meliloti exoK mutants induced pink nodules and synthesized a reduced amount of exopolysaccharide (EPS). Colonies of this mutant showed a delay in the appearance of the Calcofluor white fluorescence. In addition, the formation of the characteristic halo was strongly delayed. R. meliloti exoL and exoH mutants induced pseudonodules. The exoH, but not the exoL mutant, synthesized an EPS that could be precipitated by cetyl pyridinium chloride (CPC) and also by ethanol. Plasmid integration mutagenesis revealed promoter regions preceding exoH, exoK and exoL.
Stichworte
ENDO-BETA-1;
ACIDIC EXOPOLYSACCHARIDE (EPS);
RHIZOBIUM-MELILOTI;
ALFALFA NODULE;
NUCLEOTIDE SEQUENCE;
INFECTION;
3-1;
4-GLUCANASE
Erscheinungsjahr
1993
Zeitschriftentitel
Mol Gen Genet
Band
238
Ausgabe
1-2
Seite(n)
145-154
ISSN
0026-8925
Page URI
https://pub.uni-bielefeld.de/record/1645781
Zitieren
BECKER A, KLEICKMANN A, Arnold W, Pühler A. Analysis of the Rhizobium meliloti exoH/exoK/exoL fragment: ExoK shows homology to excreted endo-beta-1,3-1,4-glucanases and ExoH resembles membrane proteins. Mol Gen Genet. 1993;238(1-2):145-154.
BECKER, A., KLEICKMANN, A., Arnold, W., & Pühler, A. (1993). Analysis of the Rhizobium meliloti exoH/exoK/exoL fragment: ExoK shows homology to excreted endo-beta-1,3-1,4-glucanases and ExoH resembles membrane proteins. Mol Gen Genet, 238(1-2), 145-154. https://doi.org/10.1007/BF00279541
BECKER, A, KLEICKMANN, A, Arnold, Walter, and Pühler, Alfred. 1993. “Analysis of the Rhizobium meliloti exoH/exoK/exoL fragment: ExoK shows homology to excreted endo-beta-1,3-1,4-glucanases and ExoH resembles membrane proteins”. Mol Gen Genet 238 (1-2): 145-154.
BECKER, A., KLEICKMANN, A., Arnold, W., and Pühler, A. (1993). Analysis of the Rhizobium meliloti exoH/exoK/exoL fragment: ExoK shows homology to excreted endo-beta-1,3-1,4-glucanases and ExoH resembles membrane proteins. Mol Gen Genet 238, 145-154.
BECKER, A., et al., 1993. Analysis of the Rhizobium meliloti exoH/exoK/exoL fragment: ExoK shows homology to excreted endo-beta-1,3-1,4-glucanases and ExoH resembles membrane proteins. Mol Gen Genet, 238(1-2), p 145-154.
A. BECKER, et al., “Analysis of the Rhizobium meliloti exoH/exoK/exoL fragment: ExoK shows homology to excreted endo-beta-1,3-1,4-glucanases and ExoH resembles membrane proteins”, Mol Gen Genet, vol. 238, 1993, pp. 145-154.
BECKER, A., KLEICKMANN, A., Arnold, W., Pühler, A.: Analysis of the Rhizobium meliloti exoH/exoK/exoL fragment: ExoK shows homology to excreted endo-beta-1,3-1,4-glucanases and ExoH resembles membrane proteins. Mol Gen Genet. 238, 145-154 (1993).
BECKER, A, KLEICKMANN, A, Arnold, Walter, and Pühler, Alfred. “Analysis of the Rhizobium meliloti exoH/exoK/exoL fragment: ExoK shows homology to excreted endo-beta-1,3-1,4-glucanases and ExoH resembles membrane proteins”. Mol Gen Genet 238.1-2 (1993): 145-154.
GenBank
Daten bereitgestellt von European Bioinformatics Institute (EBI)
UNIPROT
3 Einträge gefunden, die diesen Artikel zitieren
Endo-1,3-1,4-beta-glycanase ExoK (UNIPROT: P33693)
Organism: Rhizobium meliloti (strain 1021)
Download in FASTA format
Organism: Rhizobium meliloti (strain 1021)
Download in FASTA format
Succinoglycan biosynthesis protein ExoL (UNIPROT: P33694)
Organism: Rhizobium meliloti (strain 1021)
Download in FASTA format
Organism: Rhizobium meliloti (strain 1021)
Download in FASTA format
Succinoglycan biosynthesis protein ExoH (UNIPROT: P33692)
Organism: Rhizobium meliloti (strain 1021)
Download in FASTA format
Organism: Rhizobium meliloti (strain 1021)
Download in FASTA format
EMBL
1 Eintrag gefunden, die diesen Artikel zitieren
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Long S, Reed JW, Himawan J, Walker GC., J. Bacteriol. 170(9), 1988
PMID: 2842306
Long S, Reed JW, Himawan J, Walker GC., J. Bacteriol. 170(9), 1988
PMID: 2842306
Physical and genetic characterization of symbiotic and auxotrophic mutants of Rhizobium meliloti induced by transposon Tn5 mutagenesis.
Meade HM, Long SR, Ruvkun GB, Brown SE, Ausubel FM., J. Bacteriol. 149(1), 1982
PMID: 6274841
Meade HM, Long SR, Ruvkun GB, Brown SE, Ausubel FM., J. Bacteriol. 149(1), 1982
PMID: 6274841
Prediction of the secondary structure of proteins from their amino acid sequence.
Chou PY, Fasman GD., Adv. Enzymol. Relat. Areas Mol. Biol. 47(), 1978
PMID: 364941
Chou PY, Fasman GD., Adv. Enzymol. Relat. Areas Mol. Biol. 47(), 1978
PMID: 364941
A family of high-copy-number plasmid vectors with single end-label sites for rapid nucleotide sequencing.
Arnold W, Puhler A., Gene 70(1), 1988
PMID: 2907323
Arnold W, Puhler A., Gene 70(1), 1988
PMID: 2907323
Structure of the Clostridium thermocellum gene licB and the encoded beta-1,3-1,4-glucanase. A catalytic region homologous to Bacillus lichenases joined to the reiterated domain of clostridial cellulases.
Schimming S, Schwarz WH, Staudenbauer WL., Eur. J. Biochem. 204(1), 1992
PMID: 1740123
Schimming S, Schwarz WH, Staudenbauer WL., Eur. J. Biochem. 204(1), 1992
PMID: 1740123
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