scholarly article | Q13442814 |
P2093 | author name string | Alok Pandey | |
Ramesh V Sonti | |||
P2860 | cites work | The genome sequence of Xanthomonas oryzae pathovar oryzae KACC10331, the bacterial blight pathogen of rice | Q22065983 |
Comparison of the genomes of two Xanthomonas pathogens with differing host specificities | Q22122346 | ||
CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice | Q24286950 | ||
GUS fusions: beta-glucuronidase as a sensitive and versatile gene fusion marker in higher plants | Q24555861 | ||
Siderophore-based iron acquisition and pathogen control | Q24681774 | ||
Basic local alignment search tool | Q25938991 | ||
Characterization of staphyloferrin A biosynthetic and transport mutants in Staphylococcus aureus | Q27655314 | ||
Molecular properties of bacterial multidrug transporters | Q28139376 | ||
PSORTb v.2.0: expanded prediction of bacterial protein subcellular localization and insights gained from comparative proteome analysis | Q28289386 | ||
Xanthomonas campestris cell-cell communication involves a putative nucleotide receptor protein Clp and a hierarchical signalling network | Q28488500 | ||
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 | Q29615259 | ||
Feo--transport of ferrous iron into bacteria. | Q30159790 | ||
Facing the challenges of Cu, Fe and Zn homeostasis in plants | Q30499973 | ||
Mutants of Xanthomonas oryzae pv. oryzae deficient in general secretory pathway are virulence deficient and unable to secrete xylanase | Q30855602 | ||
Identification and characterization of pvuA, a gene encoding the ferric vibrioferrin receptor protein in Vibrio parahaemolyticus | Q31036094 | ||
rpfF mutants of Xanthomonas oryzae pv. oryzae are deficient for virulence and growth under low iron conditions | Q44009999 | ||
Export of the siderophore enterobactin in Escherichia coli: involvement of a 43 kDa membrane exporter | Q44030868 | ||
Erwinia chrysanthemi requires a second iron transport route dependent of the siderophore achromobactin for extracellular growth and plant infection | Q45197055 | ||
OsFRDL1 is a citrate transporter required for efficient translocation of iron in rice | Q46245101 | ||
Growth deficiency of a Xanthomonas oryzae pv. oryzae fur mutant in rice leaves is rescued by ascorbic acid supplementation | Q46617094 | ||
Characterization of a ferric uptake regulator (fur) gene from Xanthomonas campestris pv. phaseoli with unusual primary structure, genome organization, and expression patterns. | Q47914817 | ||
The csbX gene of Azotobacter vinelandii encodes an MFS efflux pump required for catecholate siderophore export. | Q48218795 | ||
Universal chemical assay for the detection and determination of siderophores. | Q50905929 | ||
Involvement of the Vibrio parahaemolyticus pvsC gene in export of the siderophore vibrioferrin. | Q51102207 | ||
A novel Porphyromonas gingivalis FeoB plays a role in manganese accumulation. | Q51462032 | ||
Identification and analysis of a siderophore biosynthetic gene cluster from Agrobacterium tumefaciens C58. | Q52561075 | ||
Coupled expression of MhpE aldolase and MhpF dehydrogenase in Escherichia coli. | Q53617331 | ||
Small, stable shuttle vectors for use in Xanthomonas. | Q54327800 | ||
Escherichia coli K-12 ferrous iron uptake mutants are impaired in their ability to colonize the mouse intestine. | Q54660430 | ||
The molecular genetics of virulence of Xanthomonas campestris | Q64449422 | ||
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) | Q73836714 | ||
Iron acquisition and virulence in Helicobacter pylori: a major role for FeoB, a high-affinity ferrous iron transporter | Q74130037 | ||
Xanthomonas oryzae pathovars: model pathogens of a model crop | Q84315614 | ||
Bacterial genes induced within the nodule during the Rhizobium-legume symbiosis | Q31317183 | ||
Plant carbohydrate scavenging through tonB-dependent receptors: a feature shared by phytopathogenic and aquatic bacteria | Q33274647 | ||
The major facilitator superfamily-type transporter YmfE and the multidrug-efflux activator Mta mediate bacillibactin secretion in Bacillus subtilis | Q33337719 | ||
Bacterial solutions to the iron-supply problem | Q33594207 | ||
Bordetella AlcS transporter functions in alcaligin siderophore export and is central to inducer sensing in positive regulation of alcaligin system gene expression | Q33788545 | ||
Iron and oxidative stress in bacteria | Q33808433 | ||
Siderophores: Structure and Function of Microbial Iron Transport Compounds | Q34058117 | ||
Legionella pneumophila feoAB promotes ferrous iron uptake and intracellular infection | Q34132560 | ||
Whole-genome comparative analysis of three phytopathogenic Xylella fastidiosa strains | Q34156241 | ||
lbtA and lbtB are required for production of the Legionella pneumophila siderophore legiobactin | Q34353950 | ||
A widely distributed bacterial pathway for siderophore biosynthesis independent of nonribosomal peptide synthetases | Q34395738 | ||
The membrane protein FeoB contains an intramolecular G protein essential for Fe(II) uptake in bacteria | Q34415897 | ||
Genetics and assembly line enzymology of siderophore biosynthesis in bacteria | Q34647692 | ||
Structural biology of bacterial iron uptake | Q34698686 | ||
The complete genome, comparative and functional analysis of Stenotrophomonas maltophilia reveals an organism heavily shielded by drug resistance determinants | Q34770892 | ||
The versatility and adaptation of bacteria from the genus Stenotrophomonas. | Q34987030 | ||
Major role for FeoB in Campylobacter jejuni ferrous iron acquisition, gut colonization, and intracellular survival | Q35073883 | ||
Pyoverdin is essential for virulence of Pseudomonas aeruginosa | Q35468143 | ||
Genetic organization of the yersiniabactin biosynthetic region and construction of avirulent mutants in Yersinia pestis | Q35546294 | ||
Yersiniabactin is a virulence factor for Klebsiella pneumoniae during pulmonary infection | Q35689457 | ||
Induction of nitrogen-fixing nodules on clover requires only 32 kilobase pairs of DNA from the Rhizobium trifolii symbiosis plasmid | Q36212792 | ||
Relationship of siderophore-mediated iron assimilation to virulence in crown gall disease | Q36307542 | ||
The iron stimulon of Xylella fastidiosa includes genes for type IV pilus and colicin V-like bacteriocins | Q36540444 | ||
Comparative analysis of FUR regulons in gamma-proteobacteria | Q39516015 | ||
Rapid gene inactivation in Pseudomonas aeruginosa | Q39553995 | ||
Acquisition of Mn(II) in addition to Fe(II) is required for full virulence of Salmonella enterica serovar Typhimurium | Q39663606 | ||
Consensus-degenerate hybrid oligonucleotide primers for amplification of distantly related sequences | Q39723424 | ||
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. | Q39847951 | ||
Characterization of the ferrous iron uptake system of Escherichia coli | Q39937148 | ||
Outer membrane protein mediating iron uptake via pyoverdinpss, the fluorescent siderophore produced by Pseudomonas syringae pv. syringae | Q39956903 | ||
Identification and characterization of genes required for biosynthesis and transport of the siderophore vibrioferrin in Vibrio parahaemolyticus | Q40173872 | ||
Ralstonia solanacearum iron scavenging by the siderophore staphyloferrin B is controlled by PhcA, the global virulence regulator | Q40420407 | ||
Detection, isolation, and characterization of siderophores | Q40687475 | ||
Salicylic acid, yersiniabactin, and pyoverdin production by the model phytopathogen Pseudomonas syringae pv. tomato DC3000: synthesis, regulation, and impact on tomato and Arabidopsis host plants | Q42103491 | ||
The organization of intercistronic regions of the aerobactin operon of pColV-K30 may account for the differential expression of the iucABCD iutA genes | Q42596616 | ||
RecD plays an essential function during growth at low temperature in the antarctic bacterium Pseudomonas syringae Lz4W. | Q42659722 | ||
Dual role of desferrioxamine in Erwinia amylovora pathogenicity | Q42681514 | ||
P433 | issue | 12 | |
P921 | main subject | Xanthomonas oryzae | Q8043056 |
P304 | page(s) | 3187-3203 | |
P577 | publication date | 2010-04-09 | |
P1433 | published in | Journal of Bacteriology | Q478419 |
P1476 | title | Role of the FeoB protein and siderophore in promoting virulence of Xanthomonas oryzae pv. oryzae on rice | |
P478 | volume | 192 |
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Q33971189 | A novel manganese efflux system, YebN, is required for virulence by Xanthomonas oryzae pv. oryzae. |
Q38673867 | Bacterial ferrous iron transport: the Feo system |
Q34447422 | Catecholate siderophores protect bacteria from pyochelin toxicity |
Q35006045 | Cell wall degrading enzyme induced rice innate immune responses are suppressed by the type 3 secretion system effectors XopN, XopQ, XopX and XopZ of Xanthomonas oryzae pv. oryzae |
Q41471954 | Cell-cell signalling promotes ferric iron uptake in Xanthomonas oryzae pv. oryzicola that contribute to its virulence and growth inside rice |
Q36208325 | Co-regulation of Iron Metabolism and Virulence Associated Functions by Iron and XibR, a Novel Iron Binding Transcription Factor, in the Plant Pathogen Xanthomonas |
Q38293254 | Deciphering the regulon of a GntR family regulator via transcriptome and ChIP-exo analyses and its contribution to virulence in Xanthomonas citri |
Q90114188 | Different Cell Wall-Degradation Ability Leads to Tissue-Specificity between Xanthomonas oryzae pv. oryzae and Xanthomonas oryzae pv. oryzicola |
Q64121854 | Functional characterization of a putative DNA methyltransferase, EadM, in Xanthomonas axonopodis pv. glycines by proteomic and phenotypic analyses |
Q45213190 | Identification and structural characterization of serobactins, a suite of lipopeptide siderophores produced by the grass endophyte Herbaspirillum seropedicae |
Q34288184 | Nutritional immunity: transition metals at the pathogen-host interface |
Q91969393 | Phylogenomic Insights into Diversity and Evolution of Nonpathogenic Xanthomonas Strains Associated with Citrus |
Q46430349 | Proteome wide identification of iron binding proteins of Xanthomonas translucens pv. undulosa: focus on secretory virulent proteins. |
Q41910749 | Requirement of siderophore biosynthesis for plant colonization by Salmonella enterica |
Q35860232 | Rice Xa21 primed genes and pathways that are critical for combating bacterial blight infection |
Q46677878 | Role of DetR in defence is critical for virulence of Xanthomonas oryzae pv. oryzae |
Q38061497 | Role of iron homeostasis in the virulence of phytopathogenic bacteria: an 'à la carte' menu. |
Q43074388 | Siderophore-mediated iron acquisition influences motility and is required for full virulence of the xylem-dwelling bacterial phytopathogen Pantoea stewartii subsp. stewartii |
Q54328493 | The ColRS system of Xanthomonas oryzae pv. oryzae is required for virulence and growth in iron-limiting conditions. |
Q38264902 | The Lysobacter capsici AZ78 Genome Has a Gene Pool Enabling it to Interact Successfully with Phytopathogenic Microorganisms and Environmental Factors. |
Q58572807 | The Xylanase BcXyl1 Modulates Plant Immunity |
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Q57751873 | Toward a mechanistic understanding of Feo-mediated ferrous iron uptake |
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Q59666097 | Xanthoferrin, the α -hydroxycarboxylate-type siderophore of Xanthomonas campestris pv. campestris , is required for optimum virulence and growth inside cabbage |
Q60362569 | Xanthomonas oryzae pv. oryzae chemotaxis components and chemoreceptor Mcp2 are involved in the sensing of constituents of xylem sap and contribute to the regulation of virulence-associated functions and entry into rice |
Q34977331 | gltB/D mutants of Xanthomonas oryzae pv. oryzae are virulence deficient |
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