Fine-tuning of galactoglucan biosynthesis in Sinorhizobium meliloti by differential wggR (expG)-, PhoB-, and mucR-dependent regulation of two promoters

Bahlawane C, Baumgarth B, Serrania J, Rueberg S, Becker A (2008)
JOURNAL OF BACTERIOLOGY 190(10): 3456-3466.

Zeitschriftenaufsatz | Veröffentlicht | Englisch
 
Download
Es wurden keine Dateien hochgeladen. Nur Publikationsnachweis!
DOI
Autor*in
Bahlawane, Christelle; Baumgarth, Birgit; Serrania, Javier; Rueberg, Silvia; Becker, Anke
Einrichtung
Centrum für Biotechnologie > Institut für Genomforschung und Systembiologie
Erscheinungsjahr
2008
Zeitschriftentitel
JOURNAL OF BACTERIOLOGY
Band
190
Ausgabe
10
Seite(n)
3456-3466
ISSN
0021-9193
Page URI
https://pub.uni-bielefeld.de/record/1588013

Zitieren

Bahlawane C, Baumgarth B, Serrania J, Rueberg S, Becker A. Fine-tuning of galactoglucan biosynthesis in Sinorhizobium meliloti by differential wggR (expG)-, PhoB-, and mucR-dependent regulation of two promoters. JOURNAL OF BACTERIOLOGY. 2008;190(10):3456-3466.
Bahlawane, C., Baumgarth, B., Serrania, J., Rueberg, S., & Becker, A. (2008). Fine-tuning of galactoglucan biosynthesis in Sinorhizobium meliloti by differential wggR (expG)-, PhoB-, and mucR-dependent regulation of two promoters. JOURNAL OF BACTERIOLOGY, 190(10), 3456-3466. https://doi.org/10.1128/JB.00062-08
Bahlawane, Christelle, Baumgarth, Birgit, Serrania, Javier, Rueberg, Silvia, and Becker, Anke. 2008. “Fine-tuning of galactoglucan biosynthesis in Sinorhizobium meliloti by differential wggR (expG)-, PhoB-, and mucR-dependent regulation of two promoters”. JOURNAL OF BACTERIOLOGY 190 (10): 3456-3466.
Bahlawane, C., Baumgarth, B., Serrania, J., Rueberg, S., and Becker, A. (2008). Fine-tuning of galactoglucan biosynthesis in Sinorhizobium meliloti by differential wggR (expG)-, PhoB-, and mucR-dependent regulation of two promoters. JOURNAL OF BACTERIOLOGY 190, 3456-3466.
Bahlawane, C., et al., 2008. Fine-tuning of galactoglucan biosynthesis in Sinorhizobium meliloti by differential wggR (expG)-, PhoB-, and mucR-dependent regulation of two promoters. JOURNAL OF BACTERIOLOGY, 190(10), p 3456-3466.
C. Bahlawane, et al., “Fine-tuning of galactoglucan biosynthesis in Sinorhizobium meliloti by differential wggR (expG)-, PhoB-, and mucR-dependent regulation of two promoters”, JOURNAL OF BACTERIOLOGY, vol. 190, 2008, pp. 3456-3466.
Bahlawane, C., Baumgarth, B., Serrania, J., Rueberg, S., Becker, A.: Fine-tuning of galactoglucan biosynthesis in Sinorhizobium meliloti by differential wggR (expG)-, PhoB-, and mucR-dependent regulation of two promoters. JOURNAL OF BACTERIOLOGY. 190, 3456-3466 (2008).
Bahlawane, Christelle, Baumgarth, Birgit, Serrania, Javier, Rueberg, Silvia, and Becker, Anke. “Fine-tuning of galactoglucan biosynthesis in Sinorhizobium meliloti by differential wggR (expG)-, PhoB-, and mucR-dependent regulation of two promoters”. JOURNAL OF BACTERIOLOGY 190.10 (2008): 3456-3466.

20 Zitationen in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

Expression of the small regulatory RNA gene mmgR is regulated negatively by AniA and positively by NtrC in Sinorhizobium meliloti 2011.
Ceizel Borella G, Lagares A, Valverde C., Microbiology 164(1), 2018
PMID: 29214973
Novel Genes and Regulators That Influence Production of Cell Surface Exopolysaccharides in Sinorhizobium meliloti.
Barnett MJ, Long SR., J Bacteriol 200(3), 2018
PMID: 29158240
Identifying the region responsible for Brucella abortus MucR higher-order oligomer formation and examining its role in gene regulation.
Pirone L, Pitzer JE, D'Abrosca G, Fattorusso R, Malgieri G, Pedone EM, Pedone PV, Roop RM, Baglivo I., Sci Rep 8(1), 2018
PMID: 30467359
A conserved α-proteobacterial small RNA contributes to osmoadaptation and symbiotic efficiency of rhizobia on legume roots.
Robledo M, Peregrina A, Millán V, García-Tomsig NI, Torres-Quesada O, Mateos PF, Becker A, Jiménez-Zurdo JI., Environ Microbiol 19(7), 2017
PMID: 28401641
Cyclic Di-GMP Regulates Multiple Cellular Functions in the Symbiotic Alphaproteobacterium Sinorhizobium meliloti.
Schäper S, Krol E, Skotnicka D, Kaever V, Hilker R, Søgaard-Andersen L, Becker A., J Bacteriol 198(3), 2016
PMID: 26574513
Classification of phenotypic subpopulations in isogenic bacterial cultures by triple promoter probing at single cell level.
Schlüter JP, Czuppon P, Schauer O, Pfaffelhuber P, McIntosh M, Becker A., J Biotechnol 198(), 2015
PMID: 25661839
The prokaryotic zinc-finger: structure, function and comparison with the eukaryotic counterpart.
Malgieri G, Palmieri M, Russo L, Fattorusso R, Pedone PV, Isernia C., FEBS J 282(23), 2015
PMID: 26365095
Cell cycle transition from S-phase to G1 in Caulobacter is mediated by ancestral virulence regulators.
Fumeaux C, Radhakrishnan SK, Ardissone S, Théraulaz L, Frandi A, Martins D, Nesper J, Abel S, Jenal U, Viollier PH., Nat Commun 5(), 2014
PMID: 24939058
Sinorhizobium meliloti 1021 Exopolysaccharide as a Flocculant Improving Chromium(III) Oxide Removal from Aqueous Solutions.
Szewczuk-Karpisz K, Wiśniewska M, Pac M, Choma A, Komaniecka I., Water Air Soil Pollut 225(), 2014
PMID: 25132693
Sticky situations: key components that control bacterial surface attachment.
Petrova OE, Sauer K., J Bacteriol 194(10), 2012
PMID: 22389478
Role of specific quorum-sensing signals in the regulation of exopolysaccharide II production within Sinorhizobium meliloti spreading colonies.
Gao M, Coggin A, Yagnik K, Teplitski M., PLoS One 7(8), 2012
PMID: 22912712
Complex regulation of symbiotic functions is coordinated by MucR and quorum sensing in Sinorhizobium meliloti.
Mueller K, González JE., J Bacteriol 193(2), 2011
PMID: 21057009
Protective efficacy and safety of Brucella melitensis 16MΔmucR against intraperitoneal and aerosol challenge in BALB/c mice.
Arenas-Gamboa AM, Rice-Ficht AC, Kahl-McDonagh MM, Ficht TA., Infect Immun 79(9), 2011
PMID: 21708998
Environmental signals and regulatory pathways that influence exopolysaccharide production in rhizobia.
Janczarek M., Int J Mol Sci 12(11), 2011
PMID: 22174640
Absence of functional TolC protein causes increased stress response gene expression in Sinorhizobium meliloti.
Santos MR, Cosme AM, Becker JD, Medeiros JM, Mata MF, Moreira LM., BMC Microbiol 10(), 2010
PMID: 20573193
Genetic and biochemical properties of an alkaline phosphatase PhoX family protein found in many bacteria.
Zaheer R, Morton R, Proudfoot M, Yakunin A, Finan TM., Environ Microbiol 11(6), 2009
PMID: 19245529
Null mutations in Sinorhizobium meliloti exoS and chvI demonstrate the importance of this two-component regulatory system for symbiosis.
Bélanger L, Dimmick KA, Fleming JS, Charles TC., Mol Microbiol 74(5), 2009
PMID: 19843226
Novel Sinorhizobium meliloti quorum sensing positive and negative regulatory feedback mechanisms respond to phosphate availability.
McIntosh M, Meyer S, Becker A., Mol Microbiol 74(5), 2009
PMID: 19889097
Competitive and cooperative effects in quorum-sensing-regulated galactoglucan biosynthesis in Sinorhizobium meliloti.
McIntosh M, Krol E, Becker A., J Bacteriol 190(15), 2008
PMID: 18515420
Sinorhizobium meliloti regulator MucR couples exopolysaccharide synthesis and motility.
Bahlawane C, McIntosh M, Krol E, Becker A., Mol Plant Microbe Interact 21(11), 2008
PMID: 18842098

58 References

Daten bereitgestellt von Europe PubMed Central.


AUTHOR UNKNOWN, 1981
mucS, a gene involved in activation of galactoglucan (EPS II) synthesis gene expression in Rhizobium meliloti.
Astete SG, Leigh JA., Mol. Plant Microbe Interact. 9(5), 1996
PMID: 8672816
Regulation at complex bacterial promoters: how bacteria use different promoter organizations to produce different regulatory outcomes.
Barnard A, Wolfe A, Busby S., Curr. Opin. Microbiol. 7(2), 2004
PMID: 15063844
Specific binding of the regulatory protein ExpG to promoter regions of the galactoglucan biosynthesis gene cluster of Sinorhizobium meliloti--a combined molecular biology and force spectroscopy investigation.
Bartels FW, Baumgarth B, Anselmetti D, Ros R, Becker A., J. Struct. Biol. 143(2), 2003
PMID: 12972351
Detailed studies of the binding mechanism of the Sinorhizobium meliloti transcriptional activator ExpG to DNA.
Baumgarth B, Bartels FW, Anselmetti D, Becker A, Ros R., Microbiology (Reading, Engl.) 151(Pt 1), 2005
PMID: 15632443
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, Puhler A., Mol. Gen. Genet. 238(1-2), 1993
PMID: 8479421
Identification and analysis of the Rhizobium meliloti exoAMONP genes involved in exopolysaccharide biosynthesis and mapping of promoters located on the exoHKLAMONP fragment.
Becker A, Kleickmann A, Keller M, Arnold W, Puhler A., Mol. Gen. Genet. 241(3-4), 1993
PMID: 8246891
Extension of the Rhizobium meliloti succinoglycan biosynthesis gene cluster: identification of the exsA gene encoding an ABC transporter protein, and the exsB gene which probably codes for a regulator of succinoglycan biosynthesis.
Becker A, Kuster H, Niehaus K, Puhler A., Mol. Gen. Genet. 249(5), 1995
PMID: 8544814
Regulation of succinoglycan and galactoglucan biosynthesis in Sinorhizobium meliloti.
Becker A, Ruberg S, Baumgarth B, Bertram-Drogatz PA, Quester I, Puhler A., J. Mol. Microbiol. Biotechnol. 4(3), 2002
PMID: 11931545
The 32-kilobase exp gene cluster of Rhizobium meliloti directing the biosynthesis of galactoglucan: genetic organization and properties of the encoded gene products.
Becker A, Ruberg S, Kuster H, Roxlau AA, Keller M, Ivashina T, Cheng HP, Walker GC, Puhler A., J. Bacteriol. 179(4), 1997
PMID: 9023225
New gentamicin-resistance and lacZ promoter-probe cassettes suitable for insertion mutagenesis and generation of transcriptional fusions.
Becker A, Schmidt M, Jager W, Puhler A., Gene 162(1), 1995
PMID: 7557413
R factor transfer in Rhizobium leguminosarum.
Beringer JE., J. Gen. Microbiol. 84(1), 1974
PMID: 4612098
The Sinorhizobium meliloti MucR protein, which is essential for the production of high-molecular-weight succinoglycan exopolysaccharide, binds to short DNA regions upstream of exoH and exoY.
Bertram-Drogatz PA, Quester I, Becker A, Puhler A., Mol. Gen. Genet. 257(4), 1998
PMID: 9529524
The regulatory protein MucR binds to a short DNA region located upstream of the mucR coding region in Rhizobium meliloti.
Bertram-Drogatz PA, Ruberg S, Becker A, Puhler A., Mol. Gen. Genet. 254(5), 1997
PMID: 9197412

AUTHOR UNKNOWN, 1973
Tandem DNA recognition by PhoB, a two-component signal transduction transcriptional activator.
Blanco AG, Sola M, Gomis-Ruth FX, Coll M., Structure 10(5), 2002
PMID: 12015152
The Rhizobium meliloti exoZl exoB fragment of megaplasmid 2: ExoB functions as a UDP-glucose 4-epimerase and ExoZ shows homology to NodX of Rhizobium leguminosarum biovar viciae strain TOM.
Buendia AM, Enenkel B, Koplin R, Niehaus K, Arnold W, Puhler A., Mol. Microbiol. 5(6), 1991
PMID: 1787800

AUTHOR UNKNOWN, 1987
Sinorhizobium meliloti differentiation during symbiosis with alfalfa: a transcriptomic dissection.
Capela D, Filipe C, Bobik C, Batut J, Bruand C., Mol. Plant Microbe Interact. 19(4), 2006
PMID: 16610739

AUTHOR UNKNOWN, 1979
The virC and virD operons of the Agrobacterium Ti plasmid are regulated by the ros chromosomal gene: analysis of the cloned ros gene.
Cooley MB, D'Souza MR, Kado CI., J. Bacteriol. 173(8), 1991
PMID: 2013576
Surface polysaccharide involvement in establishing the rhizobium-legume symbiosis.
Fraysse N, Couderc F, Poinsot V., Eur. J. Biochem. 270(7), 2003
PMID: 12653992
Infection and invasion of roots by symbiotic, nitrogen-fixing rhizobia during nodulation of temperate legumes.
Gage DJ., Microbiol. Mol. Biol. Rev. 68(2), 2004
PMID: 15187185
Rhizobium nod factor perception and signalling.
Geurts R, Bisseling T., Plant Cell 14 Suppl(), 2002
PMID: 12045280
A novel exopolysaccharide can function in place of the calcofluor-binding exopolysaccharide in nodulation of alfalfa by Rhizobium meliloti.
Glazebrook J, Walker GC., Cell 56(4), 1989
PMID: 2537152
Family of glycosyl transferases needed for the synthesis of succinoglycan by Rhizobium meliloti.
Glucksmann MA, Reuber TL, Walker GC., J. Bacteriol. 175(21), 1993
PMID: 8226645
Genes needed for the modification, polymerization, export, and processing of succinoglycan by Rhizobium meliloti: a model for succinoglycan biosynthesis.
Glucksmann MA, Reuber TL, Walker GC., J. Bacteriol. 175(21), 1993
PMID: 8226646
Rhizobium meliloti exopolysaccharides: synthesis and symbiotic function.
Gonzalez JE, York GM, Walker GC., Gene 179(1), 1996
PMID: 8955640
Rhizobium symbiosis: insight into Nod factor receptors.
Gough C., Curr. Biol. 13(24), 2003
PMID: 14680658
Expression of regulatory nif genes in Rhodobacter capsulatus.
Hubner P, Willison JC, Vignais PM, Bickle TA., J. Bacteriol. 173(9), 1991
PMID: 1902215
Molecular analysis of the Rhizobium meliloti mucR gene regulating the biosynthesis of the exopolysaccharides succinoglycan and galactoglucan.
Keller M, Roxlau A, Weng WM, Schmidt M, Quandt J, Niehaus K, Jording D, Arnold W, Puhler A., Mol. Plant Microbe Interact. 8(2), 1995
PMID: 7756693

AUTHOR UNKNOWN, 1992
Global transcriptional analysis of the phosphate starvation response in Sinorhizobium meliloti strains 1021 and 2011.
Krol E, Becker A., Mol. Genet. Genomics 272(1), 2004
PMID: 15221452
Web services at the European bioinformatics institute.
Labarga A, Valentin F, Anderson M, Lopez R., Nucleic Acids Res. 35(Web Server issue), 2007
PMID: 17576686
Exopolysaccharide-deficient mutants of Rhizobium meliloti that form ineffective nodules.
Leigh JA, Signer ER, Walker GC., Proc. Natl. Acad. Sci. U.S.A. 82(18), 1985
PMID: 3862129
Promoter prediction in the rhizobia.
MacLellan SR, MacLean AM, Finan TM., Microbiology (Reading, Engl.) 152(Pt 6), 2006
PMID: 16735738
DNA binding of PhoB and its interaction with RNA polymerase.
Makino K, Amemura M, Kawamoto T, Kimura S, Shinagawa H, Nakata A, Suzuki M., J. Mol. Biol. 259(1), 1996
PMID: 8648643
Identification of two quorum-sensing systems in Sinorhizobium meliloti.
Marketon MM, Gonzalez JE., J. Bacteriol. 184(13), 2002
PMID: 12057940
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
Environmental regulation of exopolysaccharide production in Sinorhizobium meliloti.
Mendrygal KE, Gonzalez JE., J. Bacteriol. 182(3), 2000
PMID: 10633091

AUTHOR UNKNOWN, 1972
Multiconnection of identical zinc finger: implication for DNA binding affinity and unit modulation of the three zinc finger domain.
Nagaoka M, Kaji T, Imanishi M, Hori Y, Nomura W, Sugiura Y., Biochemistry 40(9), 2001
PMID: 11258905

AUTHOR UNKNOWN, 1993
A LuxR homolog controls production of symbiotically active extracellular polysaccharide II by Sinorhizobium meliloti.
Pellock BJ, Teplitski M, Boinay RP, Bauer WD, Walker GC., J. Bacteriol. 184(18), 2002
PMID: 12193623
Bacterial polysaccharide synthesis and gene nomenclature.
Reeves PR, Hobbs M, Valvano MA, Skurnik M, Whitfield C, Coplin D, Kido N, Klena J, Maskell D, Raetz CR, Rick PD., Trends Microbiol. 4(12), 1996
PMID: 9004408
Detailed structural characterization of succinoglycan, the major exopolysaccharide of Rhizobium meliloti Rm1021.
Reinhold BB, Chan SY, Reuber TL, Marra A, Walker GC, Reinhold VN., J. Bacteriol. 176(7), 1994
PMID: 8144468
Biosynthesis of the exopolysaccharide galactoglucan in Sinorhizobium meliloti is subject to a complex control by the phosphate-dependent regulator PhoB and the proteins ExpG and MucR.
Ruberg S, Puhler A, Becker A., Microbiology (Reading, Engl.) 145 ( Pt 3)(), 1999
PMID: 10217494

AUTHOR UNKNOWN, 1989
Small mobilizable multi-purpose cloning vectors derived from the Escherichia coli plasmids pK18 and pK19: selection of defined deletions in the chromosome of Corynebacterium glutamicum.
Schafer A, Tauch A, Jager W, Kalinowski J, Thierbach G, Puhler A., Gene 145(1), 1994
PMID: 8045426
High frequency mobilization of gram-negative bacterial replicons by the in vitro constructed Tn5-Mob transposon.
Simon R., Mol. Gen. Genet. 196(3), 1984
PMID: 6094969

AUTHOR UNKNOWN, 1983
Use of bacteriophage T7 RNA polymerase to direct selective high-level expression of cloned genes.
Studier FW, Moffatt BA., J. Mol. Biol. 189(1), 1986
PMID: 3537305
Genes coding for phosphotransacetylase and acetate kinase in Sinorhizobium meliloti are in an operon that is inducible by phosphate stress and controlled by phoB.
Summers ML, Denton MC, McDermott TR., J. Bacteriol. 181(7), 1999
PMID: 10094701
A bacteriophage T7 RNA polymerase/promoter system for controlled exclusive expression of specific genes.
Tabor S, Richardson CC., Proc. Natl. Acad. Sci. U.S.A. 82(4), 1985
PMID: 3156376
Genomics insights into symbiotic nitrogen fixation.
Weidner S, Puhler A, Kuster H., Curr. Opin. Biotechnol. 14(2), 2003
PMID: 12732321
Genome prediction of PhoB regulated promoters in Sinorhizobium meliloti and twelve proteobacteria.
Yuan ZC, Zaheer R, Morton R, Finan TM., Nucleic Acids Res. 34(9), 2006
PMID: 16717279
Regulation and properties of PstSCAB, a high-affinity, high-velocity phosphate transport system of Sinorhizobium meliloti.
Yuan ZC, Zaheer R, Finan TM., J. Bacteriol. 188(3), 2006
PMID: 16428413
Induction of the second exopolysaccharide (EPSb) in Rhizobium meliloti SU47 by low phosphate concentrations.
Zhan HJ, Lee CC, Leigh JA., J. Bacteriol. 173(22), 1991
PMID: 1938929
Export

Markieren/ Markierung löschen
Markierte Publikationen

Open Data PUB

Web of Science

Dieser Datensatz im Web of Science®
Quellen

PMID: 18344362
PubMed | Europe PMC

Suchen in

Google Scholar