Unusual structure of the tonB-exb DNA region of Xanthomonas campestris pv. campestris: tonB, exbB, and exbD1 are essential for ferric iron uptake, but exbD2 is not

Wiggerich HG, Klauke B, Koplan R, Priefer UB, Pühler A (1997)
JOURNAL OF BACTERIOLOGY 179(22): 7103-7110.

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Autor*in
Wiggerich, HG; Klauke, B; Koplan, R; Priefer, UB; Pühler, AlfredUniBi
Abstract / Bemerkung
The nucleotide sequence of a 3.6-kb HindIII-SmaI DNA fragment of Xanthomonas campestris pv. campestris revealed four open reading frames which, based on sequence homologies, were designated tonB, exbB, exbD1, and exbD2. Analysis of translational fusions to alkaline phosphatase and beta-galactosidase confirmed that the TonB, ExbB, ExbD1, and ExbD2 proteins are anchored in the cytoplasmic membrane. The TonB protein of X. campestris pv. campestris lacks the conserved (Glu-Pro)(n) and (Lys-Pro)(m) repeats but harbors a 13-fold repeat of proline residues. By mutational analysis, the tonB, exbB, and exbD1 genes were shown to be essential for ferric iron import in X. campestris pv. campestris. In contrast, the exbD2 gene is not involved in the uptake of ferric iron.
Erscheinungsjahr
1997
Zeitschriftentitel
JOURNAL OF BACTERIOLOGY
Band
179
Ausgabe
22
Seite(n)
7103-7110
ISSN
0021-9193
Page URI
https://pub.uni-bielefeld.de/record/1626887

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Wiggerich HG, Klauke B, Koplan R, Priefer UB, Pühler A. Unusual structure of the tonB-exb DNA region of Xanthomonas campestris pv. campestris: tonB, exbB, and exbD1 are essential for ferric iron uptake, but exbD2 is not. JOURNAL OF BACTERIOLOGY. 1997;179(22):7103-7110.
Wiggerich, H. G., Klauke, B., Koplan, R., Priefer, U. B., & Pühler, A. (1997). Unusual structure of the tonB-exb DNA region of Xanthomonas campestris pv. campestris: tonB, exbB, and exbD1 are essential for ferric iron uptake, but exbD2 is not. JOURNAL OF BACTERIOLOGY, 179(22), 7103-7110. https://doi.org/10.1128/jb.179.22.7103-7110.1997
Wiggerich, HG, Klauke, B, Koplan, R, Priefer, UB, and Pühler, Alfred. 1997. “Unusual structure of the tonB-exb DNA region of Xanthomonas campestris pv. campestris: tonB, exbB, and exbD1 are essential for ferric iron uptake, but exbD2 is not”. JOURNAL OF BACTERIOLOGY 179 (22): 7103-7110.
Wiggerich, H. G., Klauke, B., Koplan, R., Priefer, U. B., and Pühler, A. (1997). Unusual structure of the tonB-exb DNA region of Xanthomonas campestris pv. campestris: tonB, exbB, and exbD1 are essential for ferric iron uptake, but exbD2 is not. JOURNAL OF BACTERIOLOGY 179, 7103-7110.
Wiggerich, H.G., et al., 1997. Unusual structure of the tonB-exb DNA region of Xanthomonas campestris pv. campestris: tonB, exbB, and exbD1 are essential for ferric iron uptake, but exbD2 is not. JOURNAL OF BACTERIOLOGY, 179(22), p 7103-7110.
H.G. Wiggerich, et al., “Unusual structure of the tonB-exb DNA region of Xanthomonas campestris pv. campestris: tonB, exbB, and exbD1 are essential for ferric iron uptake, but exbD2 is not”, JOURNAL OF BACTERIOLOGY, vol. 179, 1997, pp. 7103-7110.
Wiggerich, H.G., Klauke, B., Koplan, R., Priefer, U.B., Pühler, A.: Unusual structure of the tonB-exb DNA region of Xanthomonas campestris pv. campestris: tonB, exbB, and exbD1 are essential for ferric iron uptake, but exbD2 is not. JOURNAL OF BACTERIOLOGY. 179, 7103-7110 (1997).
Wiggerich, HG, Klauke, B, Koplan, R, Priefer, UB, and Pühler, Alfred. “Unusual structure of the tonB-exb DNA region of Xanthomonas campestris pv. campestris: tonB, exbB, and exbD1 are essential for ferric iron uptake, but exbD2 is not”. JOURNAL OF BACTERIOLOGY 179.22 (1997): 7103-7110.

31 Zitationen in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

Comparative transcription profiling of two fermentation cultures of Xanthomonas campestris pv. campestris B100 sampled in the growth and in the stationary phase.
Alkhateeb RS, Vorhölter FJ, Steffens T, Rückert C, Ortseifen V, Hublik G, Niehaus K, Pühler A., Appl Microbiol Biotechnol 102(15), 2018
PMID: 29858955
Systems and synthetic biology perspective of the versatile plant-pathogenic and polysaccharide-producing bacterium Xanthomonas campestris.
Schatschneider S, Schneider J, Blom J, Létisse F, Niehaus K, Goesmann A, Vorhölter FJ., Microbiology 163(8), 2017
PMID: 28795660
The Role of TonB Gene in Edwardsiella ictaluri Virulence.
Abdelhamed H, Lawrence ML, Karsi A., Front Physiol 8(), 2017
PMID: 29326601
Tn5 insertion in the tonB gene promoter affects iron-related phenotypes and increases extracellular siderophore levels in Gluconacetobacter diazotrophicus.
de Paula Soares C, Rodrigues EP, de Paula Ferreira J, Simões Araújo JL, Rouws LF, Baldani JI, Vidal MS., Arch Microbiol 197(2), 2015
PMID: 25323530
Characterization of the Burkholderia mallei tonB Mutant and Its Potential as a Backbone Strain for Vaccine Development.
Mott TM, Vijayakumar S, Sbrana E, Endsley JJ, Torres AG., PLoS Negl Trop Dis 9(6), 2015
PMID: 26114445
Molecular and cellular characterisation of the zinc uptake (Znu) system of Nostoc punctiforme.
Hudek L, Pearson LA, Michalczyk A, Neilan BA, Ackland ML., FEMS Microbiol Ecol 86(2), 2013
PMID: 23710564
Utilization of heme as an iron source by marine Alphaproteobacteria in the Roseobacter clade.
Roe KL, Hogle SL, Barbeau KA., Appl Environ Microbiol 79(18), 2013
PMID: 23872569
The ColRS system of Xanthomonas oryzae pv. oryzae is required for virulence and growth in iron-limiting conditions.
Subramoni S, Pandey A, Vishnu Priya MR, Patel HK, Sonti RV., Mol Plant Pathol 13(7), 2012
PMID: 22257308
The genome of Xanthomonas campestris pv. campestris B100 and its use for the reconstruction of metabolic pathways involved in xanthan biosynthesis.
Vorhölter FJ, Schneiker S, Goesmann A, Krause L, Bekel T, Kaiser O, Linke B, Patschkowski T, Rückert C, Schmid J, Sidhu VK, Sieber V, Tauch A, Watt SA, Weisshaar B, Becker A, Niehaus K, Pühler A., J Biotechnol 134(1-2), 2008
PMID: 18304669
Plant carbohydrate scavenging through tonB-dependent receptors: a feature shared by phytopathogenic and aquatic bacteria.
Blanvillain S, Meyer D, Boulanger A, Lautier M, Guynet C, Denancé N, Vasse J, Lauber E, Arlat M., PLoS One 2(2), 2007
PMID: 17311090
A mutation in an exbD gene reduces tagetitoxin production by Pseudomonas syringae pv. tagetis.
Kong H, Patterson CD, Mitchell RE, Buyer JS, Aime MC, Lydon J., Can J Microbiol 52(11), 2006
PMID: 17215893
Comprehensive analysis of the extracellular proteins from Xanthomonas campestris pv. campestris B100.
Watt SA, Wilke A, Patschkowski T, Niehaus K., Proteomics 5(1), 2005
PMID: 15619296
Comparative analyses of Xanthomonas and Xylella complete genomes.
Moreira LM, De Souza RF, Digiampietri LA, Da Silva AC, Setubal JC., OMICS 9(1), 2005
PMID: 15805778
Comparative genomics analyses of citrus-associated bacteria.
Moreira LM, de Souza RF, Almeida NF, Setubal JC, Oliveira JC, Furlan LR, Ferro JA, da Silva AC., Annu Rev Phytopathol 42(), 2004
PMID: 15283664
Gene expression profile of the plant pathogen Xylella fastidiosa during biofilm formation in vitro.
de Souza AA, Takita MA, Coletta-Filho HD, Caldana C, Yanai GM, Muto NH, de Oliveira RC, Nunes LR, Machado MA., FEMS Microbiol Lett 237(2), 2004
PMID: 15321682
Involvement of tonB-exbBD1D2 operon in infection of Xanthomonas campestris phage phi L7.
Hung CH, Yang CF, Yang CY, Tseng YH., Biochem Biophys Res Commun 302(4), 2003
PMID: 12646254
Comparison of two Xanthomonas campestris pathovar campestris genomes revealed differences in their gene composition.
Vorhölter FJ, Thias T, Meyer F, Bekel T, Kaiser O, Pühler A, Niehaus K., J Biotechnol 106(2-3), 2003
PMID: 14651861
Involvement of the TonB system in tolerance to solvents and drugs in Pseudomonas putida DOT-T1E.
Godoy P, Ramos-González MI, Ramos JL., J Bacteriol 183(18), 2001
PMID: 11514511
Bordetella pertussis TonB, a Bvg-independent virulence determinant.
Pradel E, Guiso N, Menozzi FD, Locht C., Infect Immun 68(4), 2000
PMID: 10722583
Requirement of the Pseudomonas aeruginosa tonB gene for high-affinity iron acquisition and infection.
Takase H, Nitanai H, Hoshino K, Otani T., Infect Immun 68(8), 2000
PMID: 10899848

53 References

Daten bereitgestellt von Europe PubMed Central.

DNA sequencing with chain-terminating inhibitors.
Sanger F, Nicklen S, Coulson AR., Proc. Natl. Acad. Sci. U.S.A. 74(12), 1977
PMID: 271968
Microbial iron compounds.
Neilands JB., Annu. Rev. Biochem. 50(), 1981
PMID: 6455965
Characterization of translational initiation sites in E. coli.
Stormo GD, Schneider TD, Gold LM., Nucleic Acids Res. 10(9), 1982
PMID: 7048258
A simple method for displaying the hydropathic character of a protein.
Kyte J, Doolittle RF., J. Mol. Biol. 157(1), 1982
PMID: 7108955
Rapid and sensitive protein similarity searches.
Lipman DJ, Pearson WR., Science 227(4693), 1985
PMID: 2983426
Promoter analysis of the Xanthomonas campestris pv. campestris gum operon directing biosynthesis of the xanthan polysaccharide.
Katzen F, Becker A, Zorreguieta A, Puhler A, Ielpi L., J. Bacteriol. 178(14), 1996
PMID: 8763965
The role of iron in plant host-pathogen interactions.
Expert D, Enard C, Masclaux C., Trends Microbiol. 4(6), 1996
PMID: 8795159
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
Mechanism and control of transcription initiation in prokaryotes.
McClure WR., Annu. Rev. Biochem. 54(), 1985
PMID: 3896120
The current status and portability of our sequence handling software.
Staden R., Nucleic Acids Res. 14(1), 1986
PMID: 3511446
Transcription termination and the regulation of gene expression.
Platt T., Annu. Rev. Biochem. 55(), 1986
PMID: 3527045
Universal chemical assay for the detection and determination of siderophores.
Schwyn B, Neilands JB., Anal. Biochem. 160(1), 1987
PMID: 2952030
Linkage map of Escherichia coli K-12, edition 8.
Bachmann BJ., Microbiol. Rev. 54(2), 1990
PMID: 2194094
Import-defective colicin B derivatives mutated in the TonB box.
Mende J, Braun V., Mol. Microbiol. 4(9), 1990
PMID: 2287276
TonB and the gram-negative dilemma.
Postle K., Mol. Microbiol. 4(12), 1990
PMID: 2150975
Evidence for a TonB-dependent energy transduction complex in Escherichia coli.
Skare JT, Postle K., Mol. Microbiol. 5(12), 1991
PMID: 1809832
Site-directed mutagenesis of virtually any plasmid by eliminating a unique site.
Deng WP, Nickoloff JA., Anal. Biochem. 200(1), 1992
PMID: 1595905
Membrane topology of the Escherichia coli ExbD protein.
Kampfenkel K, Braun V., J. Bacteriol. 174(16), 1992
PMID: 1644779
Topology of the ExbB protein in the cytoplasmic membrane of Escherichia coli.
Kampfenkel K, Braun V., J. Biol. Chem. 268(8), 1993
PMID: 8449962
The TonB protein of Yersinia enterocolitica and its interactions with TonB-box proteins.
Koebnik R, Baumler AJ, Heesemann J, Braun V, Hantke K., Mol. Gen. Genet. 237(1-2), 1993
PMID: 8384290
Characterization of the ferrous iron uptake system of Escherichia coli.
Kammler M, Schon C, Hantke K., J. Bacteriol. 175(19), 1993
PMID: 8407793
Role for the outer membrane ferric siderophore receptor PupB in signal transduction across the bacterial cell envelope.
Koster M, van Klompenburg W, Bitter W, Leong J, Weisbeek P., EMBO J. 13(12), 1994
PMID: 8026465
Construction of plasmids carrying the cI gene of bacteriophage lambda.
Backman K, Ptashne M, Gilbert W., Proc. Natl. Acad. Sci. U.S.A. 73(11), 1976
PMID: 1069307
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