Plant Carbohydrate Scavenging through TonB-Dependent Receptors: A Feature Shared by Phytopathogenic and Aquatic Bacteria

TonB-dependent receptors (TBDRs) are outer membrane proteins mainly known for the active transport of iron siderophore complexes in Gram-negative bacteria. Analysis of the genome of the phytopathogenic bacterium Xanthomonas campestris pv. campestris (Xcc), predicts 72 TBDRs. Such an overrepresentation is common in Xanthomonas species but is limited to only a small number of bacteria. Here, we show that one Xcc TBDR transports sucrose with a very high affinity, suggesting that it might be a sucrose scavenger. This TBDR acts with an inner membrane transporter, an amylosucrase and a regulator to utilize sucrose, thus defining a new type of carbohydrate utilization locus, named CUT locus, involving a TBDR for the transport of substrate across the outer membrane. This sucrose CUT locus is required for full pathogenicity on Arabidopsis, showing its importance for the adaptation to host plants. A systematic analysis of Xcc TBDR genes and a genome context survey suggested that several Xcc TBDRs belong to other CUT loci involved in the utilization of various plant carbohydrates. Interestingly, several Xcc TBDRs and CUT loci are conserved in aquatic bacteria such as Caulobacter crescentus, Colwellia psychrerythraea, Saccharophagus degradans, Shewanella spp., Sphingomonas spp. or Pseudoalteromonas spp., which share the ability to degrade a wide variety of complex carbohydrates and display TBDR overrepresentation. We therefore propose that TBDR overrepresentation and the presence of CUT loci designate the ability to scavenge carbohydrates. Thus CUT loci, which seem to participate to the adaptation of phytopathogenic bacteria to their host plants, might also play a very important role in the biogeochemical cycling of plant-derived nutrients in marine environments. Moreover, the TBDRs and CUT loci identified in this study are clearly different from those characterized in the human gut symbiont Bacteroides thetaiotaomicron, which allow glycan foraging, suggesting a convergent evolution of TBDRs in Proteobacteria and Bacteroidetes.

[1]  E. Birney,et al.  Pfam: the protein families database , 2013, Nucleic Acids Res..

[2]  R. Amann,et al.  Whole genome analysis of the marine Bacteroidetes'Gramella forsetii' reveals adaptations to degradation of polymeric organic matter. , 2006, Environmental microbiology.

[3]  P. Genschik,et al.  Ralstonia solanacearum requires F-box-like domain-containing type III effectors to promote disease on several host plants , 2006, Proceedings of the National Academy of Sciences.

[4]  L. Zou,et al.  Elucidation of the hrp Clusters of Xanthomonas oryzae pv. oryzicola That Control the Hypersensitive Response in Nonhost Tobacco and Pathogenicity in Susceptible Host Rice , 2006, Applied and Environmental Microbiology.

[5]  U. Bonas,et al.  Specific Binding of the Xanthomonas campestris pv. vesicatoria AraC-Type Transcriptional Activator HrpX to Plant-Inducible Promoter Boxes , 2006, Journal of bacteriology.

[6]  Christian Boucher,et al.  PopF1 and PopF2, Two Proteins Secreted by the Type III Protein Secretion System of Ralstonia solanacearum, Are Translocators Belonging to the HrpF/NopX Family , 2006, Journal of bacteriology.

[7]  T. Schweder,et al.  Proteomic identification of a two-component regulatory system in Pseudoalteromonas haloplanktis TAC125 , 2006, Extremophiles.

[8]  D. Shultis,et al.  Outer Membrane Active Transport: Structure of the BtuB:TonB Complex , 2006, Science.

[9]  M. Allaire,et al.  Structure of TonB in Complex with FhuA, E. coli Outer Membrane Receptor , 2006, Science.

[10]  A. Furutani,et al.  Gene Involved in Transcriptional Activation of the hrp Regulatory Gene hrpG in Xanthomonas oryzae pv. oryzae , 2006, Journal of bacteriology.

[11]  J. M. Dow,et al.  Cell-cell signaling in Xanthomonas campestris involves an HD-GYP domain protein that functions in cyclic di-GMP turnover. , 2006, Proceedings of the National Academy of Sciences of the United States of America.

[12]  Paul Gillingham,et al.  Feo – Transport of Ferrous Iron into Bacteria , 2006, Biometals.

[13]  C. Vandenbroucke-Grauls,et al.  The Heterologous Siderophores Ferrioxamine B and Ferrichrome Activate Signaling Pathways in Pseudomonas aeruginosa , 2006, Journal of bacteriology.

[14]  B. Mikami,et al.  Engineered membrane superchannel improves bioremediation potential of dioxin-degrading bacteria , 2006, Nature Biotechnology.

[15]  A. Nordheim,et al.  ExbBD-Dependent Transport of Maltodextrins through the Novel MalA Protein across the Outer Membrane of Caulobacter crescentus , 2005, Journal of bacteriology.

[16]  S. Payne,et al.  Iron and Fur Regulation in Vibrio cholerae and the Role of Fur in Virulence , 2005, Infection and Immunity.

[17]  S. Schuster,et al.  Insights into Genome Plasticity and Pathogenicity of the Plant Pathogenic Bacterium Xanthomonas campestris pv. vesicatoria Revealed by the Complete Genome Sequence , 2005, Journal of bacteriology.

[18]  Masaru Takeya,et al.  Genome Sequence of Xanthomonas oryzae pv. oryzae Suggests Contribution of Large Numbers of Effector Genes and Insertion Sequences to Its Race Diversity , 2005 .

[19]  B. Mikami,et al.  Proteomics-based identification of outer-membrane proteins responsible for import of macromolecules in Sphingomonas sp. A1: alginate-binding flagellin on the cell surface. , 2005, Biochemistry.

[20]  Victor de Lorenzo,et al.  Genetically modified organisms for the environment: stories of success and failure and what we have learned from them. , 2005, International microbiology : the official journal of the Spanish Society for Microbiology.

[21]  V. Braun,et al.  Transmembrane transcriptional control (surface signalling) of the Escherichia coli Fec type. , 2005, FEMS microbiology reviews.

[22]  R. Koebnik TonB-dependent trans-envelope signalling: the exception or the rule? , 2005, Trends in microbiology.

[23]  R. Sonti,et al.  Growth deficiency of a Xanthomonas oryzae pv. oryzae fur mutant in rice leaves is rescued by ascorbic acid supplementation. , 2005, Molecular plant-microbe interactions : MPMI.

[24]  Liam J. McGuffin,et al.  Protein structure prediction servers at University College London , 2005, Nucleic Acids Res..

[25]  C. Menck,et al.  Non-gamma-proteobacteria gene islands contribute to the Xanthomonas genome. , 2005, Omics : a journal of integrative biology.

[26]  Zhijian Yao,et al.  Comparative and functional genomic analyses of the pathogenicity of phytopathogen Xanthomonas campestris pv. campestris. , 2005, Genome research.

[27]  D. Roby,et al.  Optimization of pathogenicity assays to study the Arabidopsis thaliana-Xanthomonas campestris pv. campestris pathosystem. , 2005, Molecular plant pathology.

[28]  M. Whalen,et al.  Functional analysis of the early chlorosis factor gene. , 2005, Molecular plant-microbe interactions : MPMI.

[29]  F. Bäckhed,et al.  Host-Bacterial Mutualism in the Human Intestine , 2005, Science.

[30]  Benjamin P. Westover,et al.  Glycan Foraging in Vivo by an Intestine-Adapted Bacterial Symbiont , 2005, Science.

[31]  Hyungtae Kim,et al.  The genome sequence of Xanthomonas oryzae pathovar oryzae KACC10331, the bacterial blight pathogen of rice , 2005, Nucleic acids research.

[32]  B. Mikami,et al.  Structure and Function of Bacterial Super-Biosystem Responsible for Import and Depolymerization of Macromolecules , 2005, Bioscience, biotechnology, and biochemistry.

[33]  Y. Hashidoko Ecochemical Studies of Interrelationships between Epiphytic Bacteria and Host Plants via Secondary Metabolites , 2005, Bioscience, biotechnology, and biochemistry.

[34]  V. Abratt,et al.  Sucrose utilisation in bacteria: genetic organisation and regulation , 2005, Applied Microbiology and Biotechnology.

[35]  Dorothea K. Thompson,et al.  Transcriptomic and Proteomic Characterization of the Fur Modulon in the Metal-Reducing Bacterium Shewanella oneidensis , 2004, Journal of bacteriology.

[36]  S. Brunak,et al.  Improved prediction of signal peptides: SignalP 3.0. , 2004, Journal of molecular biology.

[37]  C. Boucher,et al.  Inventory and functional analysis of the large Hrp regulon in Ralstonia solanacearum: identification of novel effector proteins translocated to plant host cells through the type III secretion system , 2004, Molecular microbiology.

[38]  J. Mattick,et al.  tonB3 Is Required for Normal Twitching Motility and Extracellular Assembly of Type IV Pili , 2004, Journal of bacteriology.

[39]  Michael Y. Galperin,et al.  Bacterial signal transduction network in a genomic perspective. , 2004, Environmental microbiology.

[40]  G. Crooks,et al.  WebLogo: a sequence logo generator. , 2004, Genome research.

[41]  C. Boucher,et al.  Characterization of the cis-Acting Regulatory Element Controlling HrpB-Mediated Activation of the Type III Secretion System and Effector Genes in Ralstonia solanacearum , 2004, Journal of bacteriology.

[42]  A. Pühler,et al.  What can bacterial genome research teach us about bacteria-plant interactions? , 2004, Current opinion in plant biology.

[43]  Alison K. Hottes,et al.  Transcriptional Profiling of Caulobacter crescentus during Growth on Complex and Minimal Media , 2004, Journal of bacteriology.

[44]  J. Graham,et al.  The leucine-responsive regulatory protein (lrp) gene for characterization of the relationship among Xanthomonas species. , 2004, International journal of systematic and evolutionary microbiology.

[45]  S. Heu,et al.  Molecular and Functional Characterization of a Unique Sucrose Hydrolase from Xanthomonas axonopodis pv. glycines , 2004, Journal of bacteriology.

[46]  J. M. Dow,et al.  Genetic and molecular analysis of a cluster of rpf genes involved in positive regulation of synthesis of extracellular enzymes and polysaccharide in Xanthomonas campestris pathovar campestris , 1991, Molecular and General Genetics MGG.

[47]  Ji-Liang Tang,et al.  Cloning of genes involved in negative regulation of production of extracellular enzymes and polysaccharide of Xanthomonas campestris pathovar campestris , 1990, Molecular and General Genetics MGG.

[48]  K. Hantke Selection procedure for deregulated iron transport mutants (fur) in Escherichia coli K 12: fur not only affects iron metabolism , 1987, Molecular and General Genetics MGG.

[49]  S. Miyoshi,et al.  Identification and Characterization of Genes Required for Biosynthesis and Transport of the Siderophore Vibrioferrin in Vibrio parahaemolyticus , 2003, Journal of bacteriology.

[50]  H. Nikaido Molecular Basis of Bacterial Outer Membrane Permeability Revisited , 2003, Microbiology and Molecular Biology Reviews.

[51]  W. Yue,et al.  Structural evidence for iron-free citrate and ferric citrate binding to the TonB-dependent outer membrane transporter FecA. , 2003, Journal of molecular biology.

[52]  J. M. Dow,et al.  Biofilm dispersal in Xanthomonas campestris is controlled by cell–cell signaling and is required for full virulence to plants , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[53]  J. Gordon,et al.  Honor thy symbionts , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[54]  R. Kadner,et al.  Touch and go: tying TonB to transport , 2003, Molecular microbiology.

[55]  David P. Chimento,et al.  Substrate-induced transmembrane signaling in the cobalamin transporter BtuB , 2003, Nature Structural Biology.

[56]  Lynn K. Carmichael,et al.  A Genomic View of the Human-Bacteroides thetaiotaomicron Symbiosis , 2003, Science.

[57]  J. Helmann,et al.  Recognition of DNA by Fur: a Reinterpretation of the Fur Box Consensus Sequence , 2002, Journal of bacteriology.

[58]  M. Lidstrom,et al.  Broad-host-range cre-lox system for antibiotic marker recycling in gram-negative bacteria. , 2002, BioTechniques.

[59]  J. Reilly,et al.  Proteomic analysis of the Caulobacter crescentus stalk indicates competence for nutrient uptake , 2002, Molecular microbiology.

[60]  P. Andrews,et al.  Profiling the alkaline membrane proteome of Caulobacter crescentus with two‐dimensional electrophoresis and mass spectrometry , 2002, Proteomics.

[61]  E. C. Teixeira,et al.  Comparison of the genomes of two Xanthomonas pathogens with differing host specificities , 2002, Nature.

[62]  K. Poole,et al.  Mutational Analysis of the TonB1 Energy Coupler of Pseudomonas aeruginosa , 2002, Journal of bacteriology.

[63]  Andrew D. Ferguson,et al.  Structural Basis of Gating by the Outer Membrane Transporter FecA , 2002, Science.

[64]  C. Boucher,et al.  A signal transfer system through three compartments transduces the plant cell contact-dependent signal controlling Ralstonia solanacearum hrp genes. , 2002, Molecular plant-microbe interactions : MPMI.

[65]  Kathleen Marchal,et al.  A higher-order background model improves the detection of promoter regulatory elements by Gibbs sampling , 2001, Bioinform..

[66]  C. Wandersman,et al.  Characterization of HasB, a Serratia marcescens TonB‐like protein specifically involved in the haemophore‐dependent haem acquisition system , 2001, Molecular microbiology.

[67]  R. Dutzler,et al.  Sucrose transport through maltoporin mutants of Escherichia coli. , 2001, Protein engineering.

[68]  U. Bonas,et al.  cDNA‐AFLP analysis unravels a genome‐wide hrpG‐regulon in the plant pathogen Xanthomonas campestris pv. vesicatoria , 2001, Molecular microbiology.

[69]  Jeremy S. Brown,et al.  A Streptococcus pneumoniae pathogenicity island encoding an ABC transporter involved in iron uptake and virulence , 2001, Molecular microbiology.

[70]  Kathleen Marchal,et al.  A Gibbs sampling method to detect over-represented motifs in the upstream regions of co-expressed genes , 2001, RECOMB.

[71]  J R Maddock,et al.  Analysis of the outer membrane proteome of Caulobacter crescentus by two‐dimensional electrophoresis and mass spectrometry , 2001, Proteomics.

[72]  Ian T. Paulsen,et al.  Complete genome sequence of Caulobacter crescentus , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[73]  S. Lindow,et al.  Appetite of an epiphyte: Quantitative monitoring of bacterial sugar consumption in the phyllosphere , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[74]  J. Michiels,et al.  Stable RK2-derived cloning vectors for the analysis of gene expression and gene function in gram-negative bacteria. , 2001, Molecular plant-microbe interactions : MPMI.

[75]  S. Payne,et al.  The two TonB systems of Vibrio cholerae: redundant and specific functions , 2001, Molecular microbiology.

[76]  M. Saier,et al.  An evolutionary alternative system for aryl beta-glucosides assimilation in bacteria. , 2001, Journal of molecular microbiology and biotechnology.

[77]  J. M. Dow,et al.  A two‐component system involving an HD‐GYP domain protein links cell–cell signalling to pathogenicity gene expression in Xanthomonas campestris , 2000, Molecular microbiology.

[78]  K. Geider,et al.  Molecular Analysis of Sucrose Metabolism ofErwinia amylovora and Influence on Bacterial Virulence , 2000, Journal of bacteriology.

[79]  Abigail A. Salyers,et al.  Characterization of Four Outer Membrane Proteins Involved in Binding Starch to the Cell Surface ofBacteroides thetaiotaomicron , 2000, Journal of bacteriology.

[80]  Ju-Young Park,et al.  Phylogenetic affiliation of the pseudomonads based on 16S rRNA sequence. , 2000, International journal of systematic and evolutionary microbiology.

[81]  C. Boucher,et al.  A bacterial sensor of plant cell contact controls the transcriptional induction of Ralstonia solanacearum pathogenicity genes , 2000, The EMBO journal.

[82]  A. Pühler,et al.  The exbD2 gene as well as the iron-uptake genes tonB, exbB and exbD1 of Xanthomonas campestris pv. campestris are essential for the induction of a hypersensitive response on pepper (Capsicum annuum). , 2000, Microbiology.

[83]  Liam J. McGuffin,et al.  The PSIPRED protein structure prediction server , 2000, Bioinform..

[84]  S. Lindow,et al.  Role of Leaf Surface Sugars in Colonization of Plants by Bacterial Epiphytes , 2000, Applied and Environmental Microbiology.

[85]  D. Faure,et al.  The salCAB operon of Azospirillum irakense, required for growth on salicin, is repressed by SalR, a transcriptional regulator that belongs to the LacI/GalR family , 2000, Molecular and General Genetics MGG.

[86]  S. Mongkolsuk,et al.  Characterization of a ferric uptake regulator (fur) gene from Xanthomonas campestris pv. phaseoli with unusual primary structure, genome organization, and expression patterns. , 1999, Gene.

[87]  D T Jones,et al.  Protein secondary structure prediction based on position-specific scoring matrices. , 1999, Journal of molecular biology.

[88]  S. Long,et al.  Bacterial genes induced within the nodule during the Rhizobium–legume symbiosis , 1999, Molecular microbiology.

[89]  V. de Lorenzo,et al.  Binding of the fur (ferric uptake regulator) repressor of Escherichia coli to arrays of the GATAAT sequence. , 1998, Journal of molecular biology.

[90]  C. Boucher,et al.  PrhA controls a novel regulatory pathway required for the specific induction of Ralstonia solanacearum hrp genes in the presence of plant cells , 1998, Molecular microbiology.

[91]  R. Overbeek,et al.  Searching for patterns in genomic data. , 1997, Trends in genetics : TIG.

[92]  J. Thompson,et al.  The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. , 1997, Nucleic acids research.

[93]  A. Pühler,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 , 1997, Journal of bacteriology.

[94]  V. Braun,et al.  Surface signaling: novel transcription initiation mechanism starting from the cell surface , 1997, Archives of Microbiology.

[95]  U. Bonas,et al.  Sequence and expression analysis of the hrpB pathogenicity operon of Xanthomonas campestris pv. vesicatoria which encodes eight proteins with similarity to components of the Hrp, Ysc, Spa, and Fli secretion systems. , 1995, Molecular plant-microbe interactions : MPMI.

[96]  B. Ahmer,et al.  Characterization of the exbBD operon of Escherichia coli and the role of ExbB and ExbD in TonB function and stability , 1995, Journal of bacteriology.

[97]  J. Swings,et al.  Reclassification of Xanthomonas , 1995 .

[98]  Steven E. Lindow,et al.  Coexistence among Epiphytic Bacterial Populations Mediated through Nutritional Resource Partitioning , 1994, Applied and environmental microbiology.

[99]  J. Thompson,et al.  CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. , 1994, Nucleic acids research.

[100]  R. Koebnik Structural organization of TonB-dependent receptors. , 1993, Trends in microbiology.

[101]  J. Lengeler,et al.  Molecular analysis of two ScrR repressors and of a ScrR–FruR hybrid repressor for sucrose and D‐fructose specific regulons from enteric bacteria , 1993, Molecular microbiology.

[102]  M. Hofnung A short course in bacterial genetics and a laboratory manual and handbook for Escherichia coli and related bacteria , 1993 .

[103]  S. Adhya,et al.  A family of bacterial regulators homologous to Gal and Lac repressors. , 1992, The Journal of biological chemistry.

[104]  Jeffrey H. Miller A Short Course in Bacterial Genetics: A Laboratory Manual and Handbook for Escherichia coli and Rela , 1992 .

[105]  Jeffrey H. Miller,et al.  A short course in bacterial genetics , 1992 .

[106]  U. Singh,et al.  Black rot of crucifers. , 1992 .

[107]  C. Boucher,et al.  Xanthomonas campestris contains a cluster of hrp genes related to the larger hrp cluster of Pseudomonas solanacearum. , 1991, Molecular plant-microbe interactions : MPMI.

[108]  K. Schmid,et al.  The sugar‐specific outer membrane channel ScrY contains functional characteristics of general diffusion pores and substrate‐specific porins , 1991, Molecular microbiology.

[109]  J. Tommassen,et al.  Carboxy-terminal phenylalanine is essential for the correct assembly of a bacterial outer membrane protein. , 1991, Journal of molecular biology.

[110]  R. Kadner Vitamin B12 transport in Escherichia coli: energy coupling between membranes , 1990, Molecular microbiology.

[111]  J. M. Dow,et al.  Extracellular proteases from Xanthomonas campestris pv. campestris, the black rot pathogen , 1990, Applied and environmental microbiology.

[112]  J. M. Dow,et al.  Nucleotide sequence of the engXCA gene encoding the major endoglucanase of Xanthomonas campestris pv. campestris. , 1990, Gene.

[113]  B. Staskawicz,et al.  Bacterial blight of soybean: regulation of a pathogen gene determining host cultivar specificity. , 1989, Science.

[114]  F. Corpet Multiple sequence alignment with hierarchical clustering. , 1988, Nucleic acids research.

[115]  V. de Lorenzo,et al.  Metal ion regulation of gene expression. Fur repressor-operator interaction at the promoter region of the aerobactin system of pColV-K30. , 1988, Journal of molecular biology.

[116]  G. Sprenger,et al.  Analysis of sucrose catabolism in Klebsiella pneumoniae and in Scr+ derivatives of Escherichia coli K12. , 1988, Journal of general microbiology.

[117]  M. Bevan,et al.  GUS fusions: beta‐glucuronidase as a sensitive and versatile gene fusion marker in higher plants. , 1987, The EMBO journal.

[118]  J. Neilands,et al.  Ferric uptake regulation protein acts as a repressor, employing iron (II) as a cofactor to bind the operator of an iron transport operon in Escherichia coli. , 1987, Biochemistry.

[119]  V. de Lorenzo,et al.  Operator sequences of the aerobactin operon of plasmid ColV-K30 binding the ferric uptake regulation (fur) repressor , 1987, Journal of bacteriology.

[120]  J. Neilands,et al.  Universal chemical assay for the detection and determination of siderophores. , 1987, Analytical biochemistry.

[121]  R. Kadner,et al.  Nucleotide sequence of the gene for the ferrienterochelin receptor FepA in Escherichia coli. Homology among outer membrane receptors that interact with TonB. , 1986, The Journal of biological chemistry.

[122]  L. C. Loon,et al.  Mechanisms of Resistance to Plant Diseases , 2001, Advances in Agricultural Biotechnology.

[123]  R. Schmitt,et al.  Plasmid-mediated uptake and metabolism of sucrose by Escherichia coli K-12 , 1982, Journal of bacteriology.

[124]  Daniel E. Dykhuizen,et al.  IN ESCHERICHIA COLI , 1981 .

[125]  Paul H. Williams,et al.  Black rot: a continuing threat to world crucifers. , 1980 .

[126]  C. Bradbeer,et al.  Transport of vitamin B12 in Escherichia coli: energy dependence , 1976, Journal of bacteriology.

[127]  Jeffrey H. Miller Experiments in molecular genetics , 1972 .

[128]  P. M. Di Girolamo,et al.  Transport of Vitamin B12 in Escherichia coli , 1971 .

[129]  P. M. Di Girolamo,et al.  Transport of vitamin B 12 in Escherichia coli. , 1971, Journal of Bacteriology.