Number of times cited according to CrossRef: 190

• 
  Shyam
  Narain Pandey, Murtaza Abid and Mirza Mohammad Abid Ali Khan, Diversity,
  Functions, and Stress Responses of Soil Microorganisms, Plant
  Microbiome: Stress Response, 10.1007/978-981-10-5514-0_1, (1-19),
  (2018).
  Crossref
  
  



• 
  Kapudeep
  Karmakar, Utpal Nath, Karaba
  N. Nataraja and Dipshikha Chakravortty,
  Root mediated uptake of Salmonella is different from phyto-pathogen and associated
  with the colonization of edible organs, BMC Plant Biology, 10.1186/s12870-018-1578-9, 18, 1,
  (2018).
  Crossref
  
  



• 
  Agnieszka
  Klonowska, Rémy Melkonian, Lucie
  Miché, Pierre Tisseyre and Lionel
  Moulin, Transcriptomic profiling of Burkholderia phymatum STM815,
  Cupriavidus taiwanensis LMG19424 and Rhizobium mesoamericanum STM3625 in response
  to Mimosa pudica root exudates illuminates the molecular basis of their nodulation
  competitiveness and symbiotic evolutionary history,
  BMC Genomics,
  10.1186/s12864-018-4487-2,
  19, 1,
  (2018).
  Crossref
  
  



• 
  Roxane
  Roquigny, Amy Novinscak, Adrien
  Biessy and Martin Filion, Pseudomonadaceae:
  From Biocontrol to Plant Growth Promotion, Rhizotrophs:
  Plant Growth Promotion to Bioremediation, 10.1007/978-981-10-4862-3_3, (39-68), (2017).
  Crossref
  
  



• 
  Andrew
  D. Farr, Philippe Remigi and Paul B. Rainey, Adaptive evolution
  by spontaneous domain fusion and protein relocalization,
  Nature Ecology & Evolution,
  10.1038/s41559-017-0283-7,
  1, 10,
  (1562-1568), (2017).
  Crossref
  
  


• 
  Peter
  A Lind, Andrew D Farr and Paul
  B Rainey, Evolutionary convergence in experimental Pseudomonas
  populations, The
  ISME Journal, 11, 3,
  (589), (2017).
  Crossref
  
  


• 
  Katty
  Ogata-Gutiérrez, Carolina Chumpitaz-Segovia,
  Jesus Lirio-Paredes, Mariella
  M. Finetti-Sialer and Doris Zúñiga-Dávila,
  Characterization and potential of plant growth promoting rhizobacteria isolated
  from native Andean crops, World
  Journal of Microbiology and Biotechnology, 33, 11,
  (2017).
  Crossref
  
  


• 
  Gaurav
  Yadav, Kanchan Vishwakarma, Shivesh Sharma, Vivek
  Kumar, Neha Upadhyay, Nitin
  Kumar, Rishi Kumar Verma, Rohit
  Mishra, Durgesh Kumar Tripathi and R. G. Upadhyay, Emerging Significance
  of Rhizospheric Probiotics and Its Impact on Plant Health: Current Perspective Towards
  Sustainable Agriculture, Probiotics and Plant
  Health, 10.1007/978-981-10-3473-2_10, (233-251),
  (2017).
  Crossref
  
  


• 
  Yunhao
  Liu, Chaitanya S. Gokhale, Paul
  B. Rainey and Xue‐Xian Zhang,
  Unravelling the complexity and redundancy of carbon catabolic repression in
  Pseudomonas fluorescens SBW25, Molecular
  Microbiology, 105, 4,
  (589-605), (2017).
  Wiley Online Library
  
  


• 
  Ramya
  Krishnan, Rahul Ravikumar Menon, Naoto Tanaka, Hans-Jürgen
  Busse, Srinivasan Krishnamurthi, Natarajan Rameshkumar and Pankaj
  Kumar Arora, Arthrobacter pokkalii sp nov, a Novel Plant Associated
  Actinobacterium with Plant Beneficial Properties, Isolated from Saline Tolerant Pokkali
  Rice, Kerala, India, PLOS
  ONE, 11, 3,
  (e0150322), (2016).
  Crossref
  
  


• 
  Simone
  Nübling, Herbert Schmidt and Agnes Weiss, Variation of the Pseudomonas
  community structure on oak leaf lettuce during storage detected by culture-dependent
  and -independent methods, International
  Journal of Food Microbiology, 216, (95),
  (2016).
  Crossref
  
  


• 
  Giancarlo
  Renella and Laura Giagnoni,
  Light dazzles from the black box: whole-cell biosensors are ready to inform
  on fundamental soil biological processes, Chemical and Biological Technologies in Agriculture, 3,
  1, (2016).
  Crossref
  
  


• 
  Jun
  Li, Wei Zhen, Dengkai
  Long, Ling Ding, Anhui
  Gong, Chenghong Xiao, Weike
  Jiang, Xiaoqing Liu, Tao
  Zhou, Luqi Huang and Gao-Feng
  Qiu, De Novo Sequencing and Assembly Analysis of the Pseudostellaria
  heterophylla Transcriptome, PLOS
  ONE, 11, 10,
  (e0164235), (2016).
  Crossref
  
  


• 
  José
  Miguel Quesada, Matilde Fernández, María Isabel Soriano, Laura
  Barrientos‐Moreno, María Antonia Llamas and
  Manuel Espinosa‐Urgel, Rhizosphere
  selection of Pseudomonas putida KT2440 variants with increased fitness associated
  to changes in gene expression, Environmental
  Microbiology Reports, 8, 5,
  (842-850), (2016).
  Wiley Online Library
  
  


• 
  Hajime
  Morimoto, Ryosuke Kadoya, Kazuhiro
  Takahashi and Yasuhiro Kasahara,
  Proteome analysis of Pseudomonas putida F1 genes induced in soil environments, Environmental Microbiology
  Reports, 8, 5,
  (825-832), (2016).
  Wiley Online Library
  
  


• 
  Marta
  Martini, Serena Moruzzi, Paolo
  Ermacora, Nazia Loi and Giuseppe
  Firrao, Quantitative real-time PCR and high-resolution melting
  (HRM) analysis for strain-specific monitoring of fluorescent pseudomonads used as
  biocontrol agents against soil-borne pathogens of food crops,
  Trends in Food Science & Technology, 46,
  2, (277), (2015).
  Crossref
  
  


• 
  Jenna
  Gallie, Eric Libby, Frederic
  Bertels, Philippe Remigi, Christian
  B. Jendresen, Gayle C. Ferguson, Nicolas Desprat, Marieke
  F. Buffing, Uwe Sauer, Hubertus
  J. E. Beaumont, Jan Martinussen, Mogens Kilstrup, Paul
  B. Rainey and Michael T. Laub,
  Bistability in a Metabolic Network Underpins the De Novo Evolution of Colony
  Switching in Pseudomonas fluorescens, PLOS Biology, 13, 3,
  (e1002109), (2015).
  Crossref
  
  


• 
  A
  Srivastava, Soil Fertility Dynamics vis-à-vis Climate Change in
  Citrus, Climate Dynamics in Horticultural Science,
  Volume Two, 10.1201/b18038-12, (179-211),
  (2015).
  Crossref
  
  


• 
  Brittan
  S. Scales, John R. Erb-Downward, Ian M. Huffnagle, John
  J. LiPuma and Gary B. Huffnagle,
  Comparative genomics of Pseudomonas fluorescens subclade III strains from human
  lungs, BMC Genomics, 16,
  1, (2015).
  Crossref
  
  


• 
  Taoufik
  Ghrairi, Olfa Ben Braiek and Khaled Hani, Detection and characterization
  of a bacteriocin, putadicin T01, produced byPseudomonas putidaisolated from hot spring
  water, APMIS, 123,
  3, (260), (2015).
  Crossref
  
  


• 
  Zeynab
  Khatamidoost, Salar Jamali, Mohammad Moradi and Roohollah
  Saberi Riseh, Effect of Iranian strains ofPseudomonasspp. on the
  control of root-knot nematodes on Pistachios, Biocontrol Science and Technology,
  25, 3,
  (291), (2015).
  Crossref
  
  


• 
  Matthew
  G. Bakker, Jacqueline M. Chaparro, Daniel K. Manter and Jorge
  M. Vivanco, Impacts of bulk soil microbial community structure
  on rhizosphere microbiomes of Zea mays, Plant and Soil, 392, 1-2,
  (115), (2015).
  Crossref
  
  


• 
  Peter
  A Lind, Andrew D Farr and Paul
  B Rainey, Experimental evolution reveals hidden diversity in evolutionary
  pathways, eLife, 4,
  (2015).
  Crossref
  
  


• 
  S.S. Boycheva, F.B. Pichler, B.D.
  Heijstra, K.E.M. Lau and S.J.
  Turner, The genetic toolbox for Acidovorax temperans, Journal of Microbiological
  Methods, 115, (129),
  (2015).
  Crossref
  
  


• 
  Shubham
  Chakravarty and Gregory Anderson,
  The Genus Pseudomonas, Practical Handbook
  of Microbiology, Third Edition, 10.1201/b17871-24,
  (321-344), (2015).
  Crossref
  
  


• 
  James
  L. O. McKellar, Jordan J. Minnell and Monica L. Gerth, A high‐throughput
  screen for ligand binding reveals the specificities of three amino acid chemoreceptors
  from seudomonas syringae pv. actinidiae, Molecular Microbiology,
  96, 4,
  (694-707), (2015).
  Wiley Online Library
  
  


• 
  Yunhao Liu, Paul
  B. Rainey and Xue‐Xian Zhang,
  Molecular mechanisms of xylose utilization by seudomonas fluorescens: overlapping
  genetic responses to xylose, xylulose, ribose and mannitol,
  Molecular Microbiology,
  98, 3,
  (553-570), (2015).
  Wiley Online Library
  
  


• 
  Susan F. Bailey, Aaron Hinz and Rees
  Kassen, Adaptive synonymous mutations in an experimentally evolved
  Pseudomonas fluorescens population, Nature
  Communications, 5, (2014).
  Crossref
  
  


• 
  C.
  E. Calderon, V. J. Carrion, A. de Vicente and F.
  M. Cazorla, darR and darS are regulatory genes that modulate 2-hexyl,
  5-propyl resorcinol transcription in Pseudomonas chlororaphis PCL1606, Microbiology, 160,
  Pt_12, (2670), (2014).
  Crossref
  
  


• 
  Elena
  Algar, F. Javier Gutierrez-Mañero, Ana Garcia-Villaraco, Daniel
  García-Seco, J. Antonio Lucas and Beatriz Ramos-Solano, The role of
  isoflavone metabolism in plant protection depends on the rhizobacterial MAMP that
  triggers systemic resistance against Xanthomonas axonopodis pv. glycines in Glycine
  max (L.) Merr. cv. Osumi, Plant
  Physiology and Biochemistry, 82, (9),
  (2014).
  Crossref
  
  


• 
  Juliana
  Almario, Davide Gobbin, Geneviève
  Défago, Yvan Moënne-Loccoz and Fabio Rezzonico, Prevalence of type
  III secretion system in effective biocontrol pseudomonads,
  Research in Microbiology,
  165, 4,
  (300), (2014).
  Crossref
  
  


• 
  Abdullah
  S. Alsohim, Tiffany B. Taylor, Glyn A. Barrett, Jenna
  Gallie, Xue‐Xian Zhang, Astrid
  E. Altamirano‐Junqueira, Louise J. Johnson,
  Paul B. Rainey and Robert
  W. Jackson, The biosurfactant viscosin produced by seudomonas
  fluorescens SBW25 aids spreading motility and plant growth promotion,
  Environmental Microbiology,
  16, 7,
  (2267-2281), (2014).
  Wiley Online Library
  
  


• 
  Brittan
  S. Scales, Robert P. Dickson, John J. LiPuma and Gary
  B. Huffnagle, Microbiology, Genomics, and Clinical Significance
  of the Pseudomonas fluorescens Species Complex, an Unappreciated Colonizer of Humans, Clinical Microbiology Reviews, 27,
  4, (927), (2014).
  Crossref
  
  


• 
  Matthieu
  Barret, Frank Egan, Jennifer
  Moynihan, John P. Morrissey, Olivier Lesouhaitier and Fergal
  O'Gara, Characterization of the SPI‐1 and Rsp type three secretion
  systems in seudomonas fluorescens F113, Environmental Microbiology Reports,
  5, 3,
  (377-386), (2013).
  Wiley Online Library
  
  


• 
  Estrella
  Duque, Jesús de la Torre, Patricia
  Bernal, M. Antonia Molina‐Henares, Miguel Alaminos, Manuel
  Espinosa‐Urgel, Amalia Roca, Matilde Fernández, Sophie
  de Bentzmann and Juan‐Luis Ramos,
  Identification of reciprocal adhesion genes in pathogenic and non‐pathogenic
  Pseudomonas, Environmental
  Microbiology, 15, 1,
  (36-48), (2012).
  Wiley Online
  Library
  
  


• 
  Carla Spence and Harsh
  Bais, Probiotics for Plants: Rhizospheric Microbiome and Plant
  Fitness, Molecular Microbial Ecology of the
  Rhizosphere,
  (713-721), (2013).
  Wiley Online Library
  
  


• 
  Sergio
  Álvarez-Pérez, Clara de Vega, Carlos M. Herrera and Martin
  Heil, Multilocus Sequence Analysis of Nectar Pseudomonads Reveals
  High Genetic Diversity and Contrasting Recombination Patterns,
  PLoS ONE, 8, 10,
  (e75797), (2013).
  Crossref
  
  


• 
  W.
  Radzki, F. J. Gutierrez Mañero, E. Algar, J.
  A. Lucas García, A. García-Villaraco and
  B. Ramos Solano, Bacterial
  siderophores efficiently provide iron to iron-starved tomato plants in hydroponics
  culture, Antonie
  van Leeuwenhoek, 104, 3,
  (321), (2013).
  Crossref
  
  


• 
  Katila
  Varivarn, Lindsey A Champa, Mark W Silby and Eduardo
  A Robleto, Colonization strategies of Pseudomonas fluorescens
  Pf0-1: activation of soil-specific genes important for diverse and specific environments, BMC Microbiology, 10.1186/1471-2180-13-92,
  13, 1,
  (92), (2013).
  Crossref
  
  


• 
  Matthieu
  Barret, Pascale Frey‐Klett, Anne‐Yvonne Guillerm‐Erckelboudt, Morgane
  Boutin, Gregory Guernec, Muriel
  Marchi, Stéphanie Daval and Alain Sarniguet, Combined Effects
  of Wheat Roots and Pathogenic Fungus Gaeumannomyces graminis var. tritici on Gene
  Expression of the Biocontrol Bacterium Pseudomonas fluorescens Pf29Arp, Molecular Microbial Ecology of the Rhizosphere, (643-653),
  (2013).
  Wiley Online Library
  
  


• 
  Martha
  G. López‐Guerrero, Miguel Á. Ramírez and
  Esperanza Martínez‐Romero,
  Rhizobial Genetic Repertoire to Inhabit Legume and Nonlegume Rhizospheres,
  Molecular Microbial Ecology of the Rhizosphere, (495-500),
  (2013).
  Wiley Online Library
  
  


• 
  María‐Isabel
  Ramos‐González, Miguel A. Matilla, José‐Miguel Quesada, Juan
  L. Ramos and Manuel Espinosa‐Urgel,
  Using Genomics to Unveil Bacterial Determinants of Rhizosphere Life Style,
  Molecular Microbial Ecology of the Rhizosphere, (5-16),
  (2013).
  Wiley Online Library
  
  


• 
  A.
  Lagzian, R. Saberi Riseh, P.
  Khodaygan, E. Sedaghati and H. Dashti, IntroducedPseudomonas fluorescensVUPf5
  as an important biocontrol agent for controllingGaeumannomyces graminisvar.triticithe
  causal agent of take-all disease in wheat, Archives Of Phytopathology And Plant Protection, 46,
  17, (2104), (2013).
  Crossref
  
  


• 
  Ana
  Segura and Juan Luis Ramos,
  Plant–bacteria interactions in the removal of pollutants,
  Current Opinion in Biotechnology, 10.1016/j.copbio.2012.09.011, 24,
  3, (467-473), (2013).
  Crossref
  
  



• 
  Y.
  Kroupitski, M. T. Brandl, R.
  Pinto, E. Belausov, D.
  Tamir-Ariel, S. Burdman and S. Sela (Saldinger),
  Identification of
  Salmonella enterica
  Genes with a Role in Persistence on Lettuce Leaves During Cold Storage by Recombinase-Based
  In Vivo Expression Technology
  , Phytopathology, 10.1094/PHYTO-10-12-0254-FI, 103,
  4, (362-372), (2013).
  Crossref
  
  


• 
  Rafael
  Rivilla, Francisco Martínez‐Granero and Marta Martín, Motility, Biofilm Formation,
  and Rhizosphere Colonization by Pseudomonas fluorescens F113, Molecular
  Microbial Ecology of the Rhizosphere, (723-732), (2013).
  Wiley
  Online Library
  
  


• 
  Yongliang Yan, Wei
  Lu, Ming Chen, Jin
  Wang, Wei Zhang, Yunhua
  Zhang, Shuzhen Ping, Claudine
  Elmerich and Min Lin, Genome
  Transcriptome Analysis and Functional Characterization of a Nitrogen‐Fixation Island
  in Root‐Associated Pseudomonas stutzeri
  , Molecular Microbial Ecology of the Rhizosphere, (851-863),
  (2013).
  Wiley Online Library
  
  


• 
  Matthieu
  Barret, Hao Tan, Frank
  Egan, John P. Morrissey, Jerry
  Reen and Fergal O'Gara, Exploiting
  New Systems‐Based Strategies to Elucidate Plant–Bacterial Interactions in the Rhizosphere,
  Molecular Microbial Ecology of the Rhizosphere, (57-68),
  (2013).
  Wiley Online Library
  
  


• 
  Robert
  W. Jackson, Xue‐Xian Zhang and Mark W. Silby, Identification and
  Mutational Activation of Niche‐Specific Genes Provide Insight into Regulatory Networks
  and Bacterial Function in Complex Environments, Molecular
  Microbial Ecology of the Rhizosphere, (875-882), (2013).
  Wiley
  Online Library
  
  


• 
  Xue‐Xian Zhang and Paul
  B. Rainey, EXPLORING THE SOCIOBIOLOGY OF PYOVERDIN‐PRODUCING PSEUDOMONAS, Evolution, 67,
  11, (3161-3174), (2013).
  Wiley Online Library
  
  


• 
  Rodrigo
  Mendes, Paolina Garbeva and Jos M. Raaijmakers, The rhizosphere
  microbiome: significance of plant beneficial, plant pathogenic, and human pathogenic
  microorganisms, FEMS
  Microbiology Reviews, 37, 5,
  (634-663), (2013).
  Wiley Online Library
  
  


• 
  Xu
  Cheng, Irene Bruijn, Menno
  Voort, Joyce E. Loper and Jos
  M. Raaijmakers, The Gac regulon of seudomonas fluorescens SBW25, Environmental Microbiology
  Reports, 5, 4,
  (608-619), (2013).
  Wiley Online Library
  
  


• 
  Claudia
  E. Calderón, Alejandro Pérez-García, Antonio de Vicente and Francisco
  M. Cazorla, ThedarGenes ofPseudomonas chlororaphisPCL1606 Are
  Crucial for Biocontrol Activity via Production of the Antifungal Compound 2-Hexyl,
  5-Propyl Resorcinol, Molecular
  Plant-Microbe Interactions, 26, 5,
  (554), (2013).
  Crossref
  
  


• 
  Luke
  A. Moe, Amino acids in the rhizosphere: From plants to microbes, American Journal of Botany, 100,
  9, (1692-1705), (2013).
  Wiley Online Library
  
  


• 
  Gayle
  C. Ferguson, Frederic Bertels and Paul B. Rainey,
  Adaptive Divergence in Experimental Populations of
  Pseudomonas fluorescens
  . V. Insight into the Niche Specialist Fuzzy Spreader Compels Revision of the Model
  Pseudomonas
  Radiation
  , Genetics, 10.1534/genetics.113.154948, 195,
  4, (1319-1335), (2013).
  Crossref
  
  


• 
  Xue‐Xian
  Zhang, Hao Chang, Sieu
  L. Tran, Jonathan C. Gauntlett, Gregory M. Cook and Paul
  B. Rainey, Variation in transport explains polymorphism of histidine
  and urocanate utilization in a natural Pseudomonas population,
  Environmental Microbiology,
  14, 8,
  (1941-1951), (2012).
  Wiley Online Library
  
  


• 
  Monica
  L. Gerth, Matteo P. Ferla and Paul B. Rainey, The origin and ecological
  significance of multiple branches for histidine utilization in Pseudomonas aeruginosa
  PAO1, Environmental
  Microbiology, 14, 8,
  (1929-1940), (2012).
  Wiley Online
  Library
  
  


• 
  Susan F. Bailey and Rees
  Kassen, Spatial Structure of Ecological Opportunity Drives Adaptation
  in a Bacterium, The
  American Naturalist, 180, 2,
  (270), (2012).
  Crossref
  
  


• 
  Christos
  Zamioudis and Corné M. J. Pieterse,
  Modulation of Host Immunity by Beneficial Microbes,
  Molecular Plant-Microbe Interactions, 25,
  2, (139), (2012).
  Crossref
  
  


• 
  Sandrine
  Ghirardi, Fabrice Dessaint, Sylvie Mazurier, Thérèse
  Corberand, Jos M. Raaijmakers, Jean-Marie Meyer, Yves
  Dessaux and Philippe Lemanceau,
  Identification of Traits Shared by Rhizosphere-Competent Strains of Fluorescent
  Pseudomonads, Microbial
  Ecology, 64, 3,
  (725), (2012).
  Crossref
  
  


• 
  Monica
  L. Gerth, Laura V. Nigon and Wayne M. Patrick, Characterization
  of the indole-3-glycerol phosphate synthase from Pseudomonas aeruginosa PAO1, The Protein Journal, 31,
  5, (359), (2012).
  Crossref
  
  


• 
  Joyce
  E. Loper, Karl A. Hassan, Dmitri
  V. Mavrodi, Edward W. Davis, Chee Kent Lim, Brenda
  T. Shaffer, Liam D. H. Elbourne, Virginia O. Stockwell, Sierra
  L. Hartney, Katy Breakwell, Marcella D. Henkels, Sasha
  G. Tetu, Lorena I. Rangel, Teresa
  A. Kidarsa, Neil L. Wilson, Judith E. van de Mortel, Chunxu
  Song, Rachel Blumhagen, Diana
  Radune, Jessica B. Hostetler, Lauren M. Brinkac, A.
  Scott Durkin, Daniel A. Kluepfel, W. Patrick Wechter, Anne
  J. Anderson, Young Cheol Kim, Leland S. Pierson, Elizabeth
  A. Pierson, Steven E. Lindow, Donald Y. Kobayashi, Jos
  M. Raaijmakers, David M. Weller, Linda S. Thomashow, Andrew
  E. Allen, Ian T. Paulsen and David S. Guttman, Comparative Genomics
  of Plant-Associated Pseudomonas spp.: Insights into Diversity and Inheritance of Traits
  Involved in Multitrophic Interactions, PLoS Genetics, 8, 7,
  (e1002784), (2012).
  Crossref
  
  


• 
  Eri
  Nishiyama, Yoshiyuki Ohtsubo, Yasuhiro Yamamoto, Yuji
  Nagata and Masataka Tsuda,
  Pivotal role of anthranilate dioxygenase genes in the adaptation of urkholderia
  multivorans ATCC 17616 in soil, FEMS
  Microbiology Letters, 330, 1,
  (46-55), (2012).
  Wiley Online
  Library
  
  


• 
  Fabiola G. Zuno-Floriano, Marion
  G. Miller, Maria L. Aldana-Madrid, Matt J. Hengel, Nilesh
  W. Gaikwad, Vladimir Tolstikov, Ana G. Contreras-Cortés and Gustavo
  Bonaventure, Effect of Acinetobacter sp on Metalaxyl Degradation
  and Metabolite Profile of Potato Seedlings (Solanum tuberosum L.) Alpha Variety, PLoS ONE,
  7, 2,
  (e31221), (2012).
  Crossref
  
  


• 
  Venant
  Nihorimbere, Hélène Cawoy, Alexandre
  Seyer, Alain Brunelle, Philippe
  Thonart and Marc Ongena, Impact
  of rhizosphere factors on cyclic lipopeptide signature from the plant beneficial strain
  acillus amyloliquefaciens S499, FEMS
  Microbiology Ecology, 79, 1,
  (176-191), (2011).
  Wiley Online
  Library
  
  


• 
  Anita H. Melnyk and Rees
  Kassen, ADAPTIVE LANDSCAPES IN EVOLVING POPULATIONS OF PSEUDOMONAS
  FLUORESCENS, Evolution, 65,
  11, (3048-3059), (2011).
  Wiley Online
  Library
  
  


• 
  Arif
  Tasleem Jan, Mudsser Azam, Arif
  Ali and Qazi Mohd. Rizwanul Haq,
  
  Novel approaches of beneficial
  Pseudomonas
  in mitigation of plant diseases – an appraisal
  , Journal of Plant
  Interactions, 10.1080/17429145.2010.541944, 6,
  4, (195-205), (2011).
  Crossref
  
  


• 
  Lisa
  Gorski, Jessica M. Duhé and Denise Flaherty, The Sigma B Operon
  Is a Determinant of Fitness for aListeria monocytogenesSerotype 4b Strain in Soil, Foodborne Pathogens and Disease, 8,
  6, (699), (2011).
  Crossref
  
  


• 
  Daniel
  P. Roberts, Scott M. Lohrke, Laurie McKenna, Dilip
  K. Lakshman, Hyesuk Kong and John Lydon, Mutation of adegSHomologue
  inEnterobacter cloacaeDecreases Colonization and Biological Control of Damping-Off
  on Cucumber, Phytopathology, 101,
  2, (271), (2011).
  Crossref
  
  


• 
  Matthieu
  Barret, John P. Morrissey and Fergal O’Gara, Functional genomics
  analysis of plant growth-promoting rhizobacterial traits involved in rhizosphere competence, Biology and Fertility of Soils, 47,
  7, (729), (2011).
  Crossref
  
  


• 
  DAFNA
  TAMIR‐ARIEL, TALLY ROSENBERG and SAUL BURDMAN, The Xanthomonas campestris
  pv. vesicatoria citH gene is expressed early in the infection process of tomato and
  is positively regulated by the TctDE two‐component regulatory system,
  Molecular Plant Pathology,
  12, 1,
  (57-71), (2010).
  Wiley Online Library
  
  


• 
  Mark
  W. Silby, Craig Winstanley, Scott A.C. Godfrey, Stuart
  B. Levy and Robert W. Jackson,
  Pseudomonas genomes: diverse and adaptable, FEMS Microbiology Reviews,
  35, 4,
  (652-680), (2011).
  Wiley Online Library
  
  


• 
  Xue‐Xian
  Zhang, Yun‐Hao Liu and Paul
  B. Rainey, CbrAB‐dependent regulation of pcnB, a poly(A) polymerase
  gene involved in polyadenylation of RNA in Pseudomonas fluorescens,
  Environmental Microbiology,
  12, 6,
  (1674-1683), (2010).
  Wiley Online Library
  
  


• 
  Eri
  Nishiyama, Yoshiyuki Ohtsubo, Yuji Nagata and Masataka
  Tsuda, Identification of Burkholderia multivorans ATCC 17616 genes
  induced in soil environment by in vivo expression technology,
  Environmental Microbiology,
  12, 9,
  (2539-2558), (2010).
  Wiley Online Library
  
  


• 
  C.
  G. Knight, X. X. Zhang, A.
  Gunn, T. Brenner, R.
  W. Jackson, S. R. Giddens, S.
  Prabhakar, N. Zitzmann and P.
  B. Rainey, Testing temperature‐induced proteomic changes in the
  plant‐associated bacterium Pseudomonas fluorescens SBW25,
  Environmental Microbiology Reports, 2,
  3, (396-402), (2009).
  Wiley Online
  Library
  
  


• 
  Jennifer Colburn-Clifford and Caitilyn
  Allen, Acbb3-Type CytochromeCOxidase Contributes toRalstonia solanacearumR3bv2
  Growth in Microaerobic Environments and to Bacterial Wilt Disease Development in Tomato, Molecular Plant-Microbe Interactions, 23,
  8, (1042), (2010).
  Crossref
  
  


• 
  N.
  Weyens, S. Monchy, J.
  Vangronsveld, S. Taghavi and D. van der Lelie, Plant-Microbe Partnerships,
  Handbook of Hydrocarbon and Lipid Microbiology, 10.1007/978-3-540-77587-4_189, (2545-2574),
  (2010).
  Crossref
  
  


• 
  Venant
  Nihorimbere, Patrick Fickers, Philippe Thonart and Marc
  Ongena, Ecological fitness of Bacillus subtilis BGS3 regarding
  production of the surfactin lipopeptide in the rhizosphere,
  Environmental Microbiology Reports, 1,
  2, (124-130), (2009).
  Wiley Online
  Library
  
  


• 
  Deepti Dwivedi, Bhavdish
  N. Johri, Kurt Ineichen, Victor
  Wray and Andres Wiemken, Impact
  of antifungals producing rhizobacteria on the performance of Vigna radiata in the
  presence of arbuscular mycorrhizal fungi, Mycorrhiza, 19, 8,
  (559), (2009).
  Crossref
  
  


• 
  Matthieu
  Barret, Pascale Frey-Klett, Anne-Yvonne Guillerm-Erckelboudt, Morgane
  Boutin, Gregory Guernec and Alain Sarniguet, Effect of Wheat Roots
  Infected with the Pathogenic FungusGaeumannomyces graminisvar.triticion Gene Expression
  of the Biocontrol BacteriumPseudomonas fluorescensPf29Arp,
  Molecular Plant-Microbe Interactions, 22,
  12, (1611), (2009).
  Crossref
  
  


• 
  Karen
  E. Gerhardt, Xiao-Dong Huang, Bernard R. Glick and Bruce
  M. Greenberg, Phytoremediation and rhizoremediation of organic
  soil contaminants: Potential and challenges, Plant Science, 176, 1,
  (20), (2009).
  Crossref
  
  


• 
  Andrew
  J. M. Howden, C. Jill Harrison and Gail M. Preston, A conserved mechanism
  for nitrile metabolism in bacteria and plants, The Plant Journal, 57, 2,
  (243-253), (2008).
  Wiley Online Library
  
  


• 
  Ana
  Segura, Sara Rodríguez‐Conde, Cayo Ramos and Juan
  L. Ramos, Bacterial responses and interactions with plants during
  rhizoremediation, Microbial
  Biotechnology, 2, 4,
  (452-464), (2009).
  Wiley Online
  Library
  
  


• 
  M. Barret, P.
  Frey‐Klett, M. Boutin, A.‐Y.
  Guillerm‐Erckelboudt, F. Martin, L. Guillot and A.
  Sarniguet, The plant pathogenic fungus Gaeumannomyces graminis
  var. tritici improves bacterial growth and triggers early gene regulations in the
  biocontrol strain Pseudomonas fluorescens Pf29Arp,
  New Phytologist,
  181, 2,
  (435-447), (2008).
  Wiley Online Library
  
  


• 
  Jan
  Sørensen, Mette Haubjerg Nicolaisen, Eliora Ron and Pascal
  Simonet, Molecular tools in rhizosphere microbiology—from single-cell
  to whole-community analysis, Plant
  and Soil, 10.1007/s11104-009-9946-8, 321,
  1-2, (483-512), (2009).
  Crossref
  
  



• 
  Mika
  T. Tarkka, Alain Sarniguet and Pascale Frey-Klett, Inter-kingdom
  encounters: recent advances in molecular bacterium–fungus interactions, Current Genetics, 10.1007/s00294-009-0241-2, 55,
  3, (233-243), (2009).
  Crossref
  
  



• 
  Michael
  J. McDonald, Stefanie M. Gehrig, Peter L. Meintjes, Xue-Xian
  Zhang and Paul B. Rainey,
  Adaptive Divergence in Experimental Populations of
  Pseudomonas fluorescens
  . IV. Genetic Constraints Guide Evolutionary Trajectories in a Parallel Adaptive Radiation
  , Genetics, 10.1534/genetics.109.107110, 183,
  3, (1041-1053), (2009).
  Crossref
  
  


• 
  Michelle
  Barr, Alison K. East, Mary
  Leonard, Tim H. Mauchline and Philip S. Poole, In vivo expression
  technology (IVET) selection of genes of Rhizobium leguminosarum biovar viciae A34
  expressed in the rhizosphere, FEMS
  Microbiology Letters, 282, 2,
  (219-227), (2008).
  Wiley Online
  Library
  
  


• 
  Xue‐Xian Zhang and Paul
  B. Rainey, Regulation of copper homeostasis in Pseudomonas fluorescens
  SBW25, Environmental
  Microbiology, 10, 12,
  (3284-3294), (2008).
  Wiley Online
  Library
  
  


• 
  LISA GORSKI, DENISE
  FLAHERTY and JESSICA M. DUHÉ,
  Comparison of the Stress Response of Listeria monocytogenes Strains with Sprout
  Colonization, Journal
  of Food Protection, 71, 8,
  (1556), (2008).
  Crossref
  
  


• 
  Marc
  Ongena and Philippe Jacques,
  Bacillus lipopeptides: versatile weapons for plant disease biocontrol, Trends in Microbiology, 16,
  3, (115), (2008).
  Crossref
  
  


• 
  J.
  Barriuso, B. Ramos Solano and F. J. Gutiérrez Mañero, Protection
  Against Pathogen and Salt Stress by Four Plant Growth-Promoting Rhizobacteria Isolated
  fromPinussp. onArabidopsis thaliana, Phytopathology, 98,
  6, (666), (2008).
  Crossref
  
  


• 
  Jorge
  Barriuso, Beatriz Ramos Solano, Rupert G. Fray, Miguel
  Cámara, Anton Hartmann and F.
  Javier Gutiérrez Mañero, Transgenic tomato plants alter quorum
  sensing in plant growth‐promoting rhizobacteria, Plant Biotechnology Journal,
  6, 5,
  (442-452), (2008).
  Wiley Online Library
  
  


• 
  Robert
  P. Ryan, Kieran Germaine, Ashley
  Franks, David J. Ryan and David
  N. Dowling, Bacterial endophytes: recent developments and applications, FEMS Microbiology Letters, 278,
  1, (1-9), (2007).
  Wiley Online
  Library
  
  


• 
  J. Barriuso, B.
  Ramos Solano, C. Santamaría, A. Daza and F.J.
  Gutiérrez Mañero, Effect of inoculation with putative plant growth‐promoting
  rhizobacteria isolated from Pinus spp. on Pinus pinea growth, mycorrhization and rhizosphere
  microbial communities, Journal
  of Applied Microbiology, 105, 5,
  (1298-1309), (2008).
  Wiley Online
  Library
  
  


• 
  Lotta Jäderlund, Maria
  Hellman, Ingvar Sundh, Mark
  J. Bailey and Janet K. Jansson,
  Use of a novel nonantibiotic triple marker gene cassette to monitor high survival
  of Pseudomonas fluorescens SBW25 on winter wheat in the field,
  FEMS Microbiology Ecology,
  63, 2,
  (156-168), (2007).
  Wiley Online Library
  
  


• 
  Dilfuza
  Egamberdiyeva and Khandakar R. Islam,
  Salt‐Tolerant Rhizobacteria: Plant Growth Promoting Traits and Physiological
  Characterization Within Ecologically Stressed Environments, Plant‐Bacteria
  Interactions,
  (257-281), (2008).
  Wiley Online Library
  
  


• 
  Christina
  D. Moon, Stephen R. Giddens, Xue‐Xian Zhang and Robert
  W. Jackson, Molecular Mechanisms Underpinning Colonization of
  a Plant by Plant Growth‐Promoting Rhizobacteria, Plant‐Bacteria
  Interactions,
  (111-128), (2008).
  Wiley Online Library
  
  


• 
  S.
  H. Miller, G. L. Mark, A.
  Franks and F. O'Gara, Pseudomonas–Plant
  Interactions, Pseudomonas, (353-376),
  (2008).
  Wiley Online Library
  
  


• 
  Marc
  Ongena, Emmanuel Jourdan, Akram
  Adam, Mathias Schäfer, Herbert
  Budzikiewicz and Philippe Thonart,
  Amino Acids, Iron, and Growth Rate as Key Factors Influencing Production of
  the Pseudomonas Putida BTP1 Benzylamine Derivative Involved in Systemic Resistance
  Induction in Different Plants, Microbial
  Ecology, 10.1007/s00248-007-9275-5, 55,
  2, (280-292), (2007).
  Crossref
  
  



• 
  Arvind
  Gulati, Praveen Rahi and Pratibha
  Vyas, Characterization of Phosphate-Solubilizing Fluorescent Pseudomonads
  from the Rhizosphere of Seabuckthorn Growing in the Cold Deserts of Himalayas, Current Microbiology, 10.1007/s00284-007-9042-3, 56,
  1, (73-79), (2007).
  Crossref
  
  



• 
  Velmurugan
  Ganesan, Rhizoremediation of Cadmium Soil Using a Cadmium-Resistant
  Plant Growth-Promoting Rhizopseudomonad, Current Microbiology, 10.1007/s00284-008-9099-7, 56, 4,
  (403-407), (2008).
  Crossref
  
  



• 
  Xue-Xian
  Zhang and Paul B. Rainey,
  Dual Involvement of CbrAB and NtrBC in the Regulation of Histidine Utilization in
  Pseudomonas fluorescens
  SBW25
  , Genetics, 10.1534/genetics.107.081984, 178,
  1, (185-195), (2008).
  Crossref
  
  


• 
  S.‐J.
  Ahn, C.‐H. Yang and D.A.
  Cooksey, Pseudomonas putida 06909 genes expressed during colonization
  on mycelial surfaces and phenotypic characterization of mutants,
  Journal of Applied Microbiology, 103,
  1, (120-132), (2006).
  Wiley Online
  Library
  
  


• 
  Ligang Wang, Xin
  Jiang, Dongyun Yan, Jinshui
  Wu, Yongrong Bian and Fang
  Wang, Behavior and fate of chlorpyrifos introduced into soil–crop
  systems by irrigation, Chemosphere, 66,
  3, (391), (2007).
  Crossref
  
  


• 
  S.
  R. Giddens, R. W. Jackson, C.
  D. Moon, M. A. Jacobs, X.-X.
  Zhang, S. M. Gehrig and P.
  B. Rainey, Mutational activation of niche-specific genes provides
  insight into regulatory networks and bacterial function in a complex environment, Proceedings of the National
  Academy of Sciences, 104, 46,
  (18247), (2007).
  Crossref
  
  


• 
  Ben
  Lugtenberg and Johan Leveau,
  Biocontrol of Plant Pathogens, The Rhizosphere, 10.1201/9781420005585.ch10, (267-296),
  (2009).
  Crossref
  
  


• 
  Xue-Xian
  Zhang and Paul B. Rainey, The
  Role of a P1-Type ATPase fromPseudomonas fluorescensSBW25 in Copper Homeostasis and
  Plant Colonization, Molecular
  Plant-Microbe Interactions, 20, 5,
  (581), (2007).
  Crossref
  
  


• 
  Daniel
  P. Roberts, Laurie F. McKenna, Scott M. Lohrke, Stephen
  Rehner and Jorge T. de Souza,
  Pyruvate dehydrogenase activity is important for colonization of seeds and roots
  by Enterobacter cloacae, Soil
  Biology and Biochemistry, 39, 8,
  (2150), (2007).
  Crossref
  
  


• 
  Christine
  V. Hawkes, Kristen M. DeAngelis and Mary K. Firestone, Root Interactions
  with Soil Microbial Communities and Processes, The
  Rhizosphere, 10.1016/B978-012088775-0/50003-3, (1-29),
  (2007).
  Crossref
  
  


• 
  Xue-Xian
  Zhang and Paul B. Rainey, Construction
  and validation of a neutrally-marked strain of Pseudomonas fluorescens SBW25, Journal of Microbiological
  Methods, 71, 1,
  (78), (2007).
  Crossref
  
  


• 
  Louise
  A. O'Sullivan, Andrew J. Weightman, T. Hefin Jones, Angela
  M. Marchbank, James M. Tiedje and Eshwar Mahenthiralingam, Identifying
  the genetic basis of ecologically and biotechnologically useful functions of the bacterium
  Burkholderia vietnamiensis, Environmental
  Microbiology, 9, 4,
  (1017-1034), (2007).
  Wiley Online
  Library
  
  


• 
  Jacob Jones, David
  J. Studholme, Christopher G. Knight and Gail M. Preston, Integrated bioinformatic
  and phenotypic analysis of RpoN‐dependent traits in the plant growth‐promoting bacterium
  Pseudomonas fluorescens SBW25, Environmental
  Microbiology, 9, 12,
  (3046-3064), (2007).
  Wiley Online
  Library
  
  


• 
  Daniel
  P. Roberts, Laurie F. McKenna, Xiaojia Hu, Scott
  M. Lohrke, Hye Suk Kong, Jorge
  T. de Souza, C. Jacyn Baker and John Lydon, Mutation in cyaA in Enterobacter
  cloacae decreases cucumber root colonization, Archives of Microbiology,
  10.1007/s00203-006-0177-6,
  187, 2,
  (101-115), (2006).
  Crossref
  
  



• 
  Wei
  E. Huang, Mark J. Bailey, Ian
  P. Thompson, Andrew S. Whiteley and Andrew J. Spiers, Single-Cell Raman
  Spectral Profiles of Pseudomonas fluorescens SBW25 Reflects in vitro and in planta
  Metabolic History, Microbial
  Ecology, 10.1007/s00248-006-9138-5, 53,
  3, (414-425), (2007).
  Crossref
  
  



• 
  Tadashi
  Fukami, Hubertus J. E. Beaumont, Xue-Xian Zhang and Paul
  B. Rainey, Immigration history controls diversification in experimental
  adaptive radiation, Nature, 10.1038/nature05629,
  446, 7134, (436-439),
  (2007).
  Crossref
  
  



• 
  Susanne
  Ude, Mark J. Bailey, Wei
  E. Huang and Andrew J. Spiers,
  The Environmental Plasmid pQBR103 Alters the Single-Cell Raman Spectral Profile
  of Pseudomonas fluorescens SBW25, Microbial
  Ecology, 10.1007/s00248-006-9191-0, 53,
  3, (494-497), (2007).
  Crossref
  
  



• 
  B.
  Ramos Solano, M. T. Pereyra de la Iglesia,
  A. Probanza, J.
  A. Lucas García, M. Megías and F. J. Gutierrez Mañero, Screening
  for PGPR to improve growth of Cistus ladanifer seedlings for reforestation of degraded
  mediterranean ecosystems, First International
  Meeting on Microbial Phosphate Solubilization,
  10.1007/978-1-4020-5765-6_7,
  (59-68), (2007).
  Crossref
  
  



• 
  Jesús
  Mercado-Blanco and Peter A. H. M. Bakker,
  Interactions between plants and beneficial Pseudomonas spp.: exploiting bacterial
  traits for crop protection, Antonie
  van Leeuwenhoek, 10.1007/s10482-007-9167-1, 92,
  4, (367-389), (2007).
  Crossref
  
  



• 
  Adrian
  Tett, Andrew J Spiers, Lisa
  C Crossman, Duane Ager, Lena
  Ciric, J Maxwell Dow, John
  C Fry, David Harris, Andrew
  Lilley, Anna Oliver, Julian
  Parkhill, Michael A Quail, Paul
  B Rainey, Nigel J Saunders, Kathy Seeger, Lori
  A S Snyder, Rob Squares, Christopher
  M Thomas, Sarah L Turner, Xue-Xian
  Zhang, Dawn Field and Mark
  J Bailey, Sequence-based analysis of pQBR103; a representative
  of a unique, transfer-proficient mega plasmid resident in the microbial community
  of sugar beet, The
  ISME Journal, 10.1038/ismej.2007.47, 1,
  4, (331-340), (2007).
  Crossref
  
  



• 
  Xue-Xian
  Zhang and Paul B. Rainey,
  Genetic Analysis of the Histidine Utilization (
  hut
  ) Genes in
  Pseudomonas fluorescens
  SBW25
  , Genetics, 10.1534/genetics.107.075713, 176,
  4, (2165-2176), (2007).
  Crossref
  
  



• 
  Eleni
  Bantinaki, Rees Kassen, Christopher
  G. Knight, Zena Robinson, Andrew
  J. Spiers and Paul B. Rainey,
  
  Adaptive Divergence in Experimental Populations of
  Pseudomonas fluorescens
  . III. Mutational Origins of Wrinkly Spreader Diversity
  , Genetics, 10.1534/genetics.106.069906, 176,
  1, (441-453), (2007).
  Crossref
  
  


• 
  Rowan
  D. H. Barrett and Graham Bell,
  THE DYNAMICS OF DIVERSIFICATION IN EVOLVING PSEUDOMONAS POPULATIONS, Evolution, 60,
  3, (484-490), (2007).
  Wiley
  Online Library
  
  


• 
  S. Tarnawski, J.
  Hamelin, M. Jossi, M.
  Aragno and N. Fromin, Phenotypic
  structure of Pseudomonas populations is altered under elevated pCO2 in the rhizosphere
  of perennial grasses, Soil
  Biology and Biochemistry, 38, 6,
  (1193), (2006).
  Crossref
  
  


• 
  P.
  D. Kiely, J. M. Haynes, C.
  H. Higgins, A. Franks, G.
  L. Mark, J. P. Morrissey and F. O'Gara, Exploiting New Systems-Based
  Strategies to Elucidate Plant-Bacterial Interactions in the Rhizosphere, Microbial Ecology, 10.1007/s00248-006-9019-y, 51,
  3, (257-266), (2006).
  Crossref
  
  


• 
  P.
  R. Darrah, D. L. Jones, G.
  J. D. Kirk and T. Roose, Modelling
  the rhizosphere: a review of methods for ‘upscaling’ to the whole‐plant scale, European Journal of Soil Science, 57,
  1, (13-25), (2006).
  Wiley Online
  Library
  
  


• 
  Genevieve
  L. Mark, John P. Morrissey, P. Higgins and Fergal
  O'Gara, Molecular‐based strategies to exploit Pseudomonas biocontrol
  strains for environmental biotechnology applications,
  FEMS Microbiology Ecology,
  56, 2,
  (167-177), (2006).
  Wiley Online Library
  
  


• 
  María
  Antonia Molina, Juan‐Luis Ramos and Manuel Espinosa‐Urgel, A two‐partner
  secretion system is involved in seed and root colonization and iron uptake by Pseudomonas
  putida KT2440, Environmental
  Microbiology, 8, 4,
  (639-647), (2005).
  Wiley Online
  Library
  
  


• 
  Rowan
  D. H. Barrett and Graham Bell,
  THE DYNAMICS OF DIVERSIFICATION IN EVOLVING PSEUDOMONAS POPULATIONS, Evolution, 10.1554/05-673.1,
  60, 3,
  (484), (2006).
  Crossref
  
  



• 
  Ramos
  Solano B., M. T. Pereyra de la Iglesia, A. Probanza, J.
  A. Lucas García, M. Megías and F. J. Gutierrez Mañero, Screening
  for PGPR to improve growth of Cistus ladanifer seedlings for reforestation of degraded
  mediterranean ecosystems, Plant
  and Soil, 10.1007/s11104-006-9055-x, 287,
  1-2, (59-68), (2006).
  Crossref
  
  



• 
  Jan
  Sørensen and Ole Nybroe, Reporter
  Genes in Bacterial Inoculants Can Monitor Life Conditions and Functions in Soil,
  Nucleic Acids and Proteins in Soil, 10.1007/3-540-29449-X_16, (375-395),
  (2006).
  Crossref
  
  



• 
  Patrick
  Goymer, Sophie G. Kahn, Jacob
  G. Malone, Stefanie M. Gehrig, Andrew J. Spiers and Paul
  B. Rainey,
  Adaptive Divergence in Experimental Populations of
  Pseudomonas fluorescens
  . II. Role of the GGDEF Regulator WspR in Evolution and Development of the Wrinkly
  Spreader Phenotype
  , Genetics, 10.1534/genetics.106.055863, 173,
  2, (515-526), (2006).
  Crossref
  
  


• 
  Mark
  J. Pallen, Scott A. Beatson and Christopher M. Bailey, Bioinformatics,
  genomics and evolution of non‐flagellar type‐III secretion systems: a Darwinian perpective⋆, FEMS Microbiology Reviews, 29,
  2, (201-229), (2008).
  Wiley Online
  Library
  
  


• 
  Lisa
  Gorski, Maria Brandl and Robert
  Mandrell, Attachment of Microorganisms to Fresh Produce,
  Microbiology of Fruits and Vegetables, 10.1201/9781420038934.ch2, (33-73),
  (2010).
  Crossref
  
  


• 
  G.
  L. Mark, J. M. Dow, P.
  D. Kiely, H. Higgins, J.
  Haynes, C. Baysse, A.
  Abbas, T. Foley, A.
  Franks, J. Morrissey and F.
  O'Gara, Transcriptome profiling of bacterial responses to root
  exudates identifies genes involved in microbe-plant interactions,
  Proceedings of the National Academy of Sciences, 102,
  48, (17454), (2005).
  Crossref
  
  


• 
  Fabio
  Rezzonico, Christian Binder, Geneviève Défago and Yvan
  Moënne-Loccoz, The Type III Secretion System of BiocontrolPseudomonas
  fluorescensKD Targets the Phytopathogenic ChromistaPythium ultimumand Promotes Cucumber
  Protection, Molecular
  Plant-Microbe Interactions, 18, 9,
  (991), (2005).
  Crossref
  
  


• 
  Joan
  G. Ehrenfeld, Beth Ravit and Kenneth Elgersma, FEEDBACK IN THE
  PLANT-SOIL SYSTEM, Annual
  Review of Environment and Resources, 30, 1,
  (75), (2005).
  Crossref
  
  


• 
  Elisa
  Gamalero, Guido Lingua, Riccardo
  Tombolini, Lorena Avidano, Barbara
  Pivato and Graziella Berta,
  Colonization of Tomato Root Seedling by Pseudomonas fluorescens 92rkG5: Spatio–temporal
  Dynamics, Localization, Organization, Viability, and Culturability,
  Microbial Ecology,
  50, 2,
  (289), (2005).
  Crossref
  
  


• 
  Rowan D. H.
  Barrett, R. Craig MacLean and Graham Bell, Experimental Evolution
  ofPseudomonas fluorescensin Simple and Complex Environments,
  The American Naturalist,
  166, 4,
  (470), (2005).
  Crossref
  
  


• 
  Maria L. Marco, Jennifer Legac and Steven
  E. Lindow, Pseudomonas syringae genes induced during colonization
  of leaf surfaces, Environmental
  Microbiology, 7, 9,
  (1379-1391), (2005).
  Wiley Online
  Library
  
  


• 
  J.
  Barriuso, M. T. Pereyra, J.
  A. Lucas García, M. Megías, F. J. Gutierrez Mañero and B.
  Ramos, Screening for Putative PGPR to Improve Establishment of
  the Symbiosis Lactarius deliciosus-Pinus sp., Microbial Ecology, 10.1007/s00248-004-0112-9, 50, 1,
  (82-89), (2005).
  Crossref
  
  


• 
  Alfred
  Pühler, Matthieu Arlat, Anke
  Becker, Michael Göttfert, John
  P Morrissey and Fergal O’Gara,
  What can bacterial genome research teach us about bacteria–plant interactions?, Current Opinion in Plant Biology, 7,
  2, (137), (2004).
  Crossref
  
  


• 
  E.
  Somers, J. Vanderleyden and M. Srinivasan, Rhizosphere Bacterial
  Signalling: A Love Parade Beneath Our Feet, Critical Reviews in Microbiology,
  30, 4,
  (205), (2004).
  Crossref
  
  


• 
  Shihui
  Yang, Nicole T. Perna, Donald
  A. Cooksey, Yasushi Okinaka, Steven E. Lindow, A.
  Mark Ibekwe, Noel T. Keen and Ching-Hong Yang, Genome-Wide Identification
  of Plant-Upregulated Genes ofErwinia chrysanthemi3937 Using a GFP-Based IVET Leaf
  Array, Molecular
  Plant-Microbe Interactions, 17, 9,
  (999), (2004).
  Crossref
  
  


• 
  Manuel
  Espinosa-Urgel, Plant-associated Pseudomonas populations: molecular
  biology, DNA dynamics, and gene transfer, Plasmid, 52, 3,
  (139), (2004).
  Crossref
  
  


• 
  Xue‐Xian
  Zhang, Andrew K. Lilley, Mark
  J. Bailey and Paul B. Rainey,
  The indigenous Pseudomonas plasmid pQBR103 encodes plant‐inducible genes, including
  three putative helicases, FEMS
  Microbiology Ecology, 51, 1,
  (9-17), (2006).
  Wiley Online
  Library
  
  


• 
  Elisa Gamalero, Guido
  Lingua, Flavia Giusy Caprì, Anna Fusconi, Graziella
  Berta and Philippe Lemanceau,
  Colonization pattern of primary tomato roots by Pseudomonas fluorescens A6RI
  characterized by dilution plating, flow cytometry, fluorescence, confocal and scanning
  electron microscopy, FEMS
  Microbiology Ecology, 48, 1,
  (79-87), (2006).
  Wiley Online
  Library
  
  


• 
  Darby G. Brown and Caitilyn
  Allen, Ralstonia solanacearum genes induced during growth in tomato:
  an inside view of bacterial wilt, Molecular
  Microbiology, 53, 6,
  (1641-1660), (2004).
  Wiley Online
  Library
  
  


• 
  Gail
  M. Preston,
  Plant perceptions of plant growth-promoting
  Pseudomonas
  , Philosophical
  Transactions of the Royal Society of London. Series B: Biological Sciences, 10.1098/rstb.2003.1384,
  359, 1446, (907-918),
  (2004).
  Crossref
  
  


• 
  Micaela
  Gal, Gail M. Preston, Ruth
  C. Massey, Andrew J. Spiers and Paul B. Rainey, Genes encoding a cellulosic
  polymer contribute toward the ecological success of Pseudomonas fluorescens SBW25
  on plant surfaces, Molecular
  Ecology, 12, 11,
  (3109-3121), (2003).
  Wiley Online
  Library
  
  


• 
  Dawn L. Arnold, Andrew
  Pitman and Robert W. Jackson,
  Pathogenicity and other genomic islands in plant pathogenic bacteria, Molecular Plant Pathology, 4,
  5, (407-420), (2003).
  Wiley Online
  Library
  
  


• 
  Pablo Vinuesa, Frauke
  Neumann-Silkow, Cristina Pacios-Bras, Herman P. Spaink, Esperanza
  Martínez-Romero and Dietrich Werner,
  Genetic Analysis of a pH-Regulated Operon fromRhizobium tropiciCIAT899 Involved
  in Acid Tolerance and Nodulation Competitiveness, Molecular Plant-Microbe Interactions,
  16, 2,
  (159), (2003).
  Crossref
  
  


• 
  F.
  PERSELLO‐CARTIEAUX, L. NUSSAUME and C. ROBAGLIA, Tales from the underground:
  molecular plant–rhizobacteria interactions, Plant, Cell & Environment,
  26, 2,
  (189-199), (2003).
  Wiley Online Library
  
  


• 
  Donald
  A. Phillips, Howard Ferris, Douglas R. Cook and Donald
  R. Strong, MOLECULAR CONTROL POINTS IN RHIZOSPHERE FOOD WEBS, Ecology,
  84, 4,
  (816-826), (2003).
  Wiley Online
  Library
  
  


• 
  Lucie Miché, Shimshon
  Belkin, Rachel Rozen and Jacques
  Balandreau, Rice seedling whole exudates and extracted alkylresorcinols
  induce stress‐response in Escherichia coli biosensors,
  Environmental Microbiology,
  5, 5,
  (403-411), (2003).
  Wiley Online Library
  
  


• 
  Gregor
  Reid, M. E. Sanders, H.
  Rex Gaskins, Glenn R. Gibson, Annick Mercenier, Robert
  Rastall, Marcel Roberfroid, Ian Rowland, Christine
  Cherbut and Todd R. Klaenhammer,
  New Scientific Paradigms for Probiotics and Prebiotics,
  Journal of Clinical Gastroenterology, 37,
  2, (105), (2003).
  Crossref
  
  


• 
  Bhavdish
  N. Johri, A. Sharma and J.
  S. Virdi, Rhizobacterial Diversity in India and Its Influence
  on Soil and Plant Health, Biotechnology in
  India I, 10.1007/3-540-36488-9_2, (49-89),
  (2003).
  Crossref
  
  


• 
  Jan
  Dirk Elsas and Mark J. Bailey,
  The ecology of transfer of mobile genetic elements,
  FEMS Microbiology Ecology,
  42, 2,
  (187-197), (2006).
  Wiley Online Library
  
  


• 
  S.L.
  Turner, M.J. Bailey, A.K.
  Lilley and C.M. Thomas, Ecological
  and molecular maintenance strategies of mobile genetic elements,
  FEMS Microbiology Ecology,
  42, 2,
  (177-185), (2006).
  Wiley Online Library
  
  


• 
  Isabelle
  Hautefort and Jay C.D. Hinton,
  4 Molecular methods for monitoring bacterial gene expression during infection,
  Molecular Cellular Microbiology, 10.1016/S0580-9517(02)31005-5, (55-91),
  (2002).
  Crossref
  
  



• 
  Seon-Woo
  Lee, In Vivo Expression Technology (IVET) and Its Application
  in Plant-Associated Bacteria, The
  Plant Pathology Journal, 10.5423/PPJ.2002.18.2.057, 18,
  2, (57-62), (2002).
  Crossref
  
  


• 
  G
  Carrillo-Castañeda, J Juárez Muños, J.R Peralta-Videa, E
  Gomez, K.J Tiemannb, M
  Duarte-Gardea and J.L Gardea-Torresdey,
  Alfalfa growth promotion by bacteria grown under iron limiting conditions, Advances in Environmental
  Research, 6, 3,
  (391), (2002).
  Crossref
  
  


• 
  Jens
  Boch, Vinita Joardar, Lisa
  Gao, Tara L. Robertson, Melisa
  Lim and Barbara N. Kunkel,
  Identification of Pseudomonas syringae pv. tomato genes induced
  during infection of Arabidopsis thaliana, Molecular Microbiology,
  44, 1,
  (73-88), (2002).
  Wiley Online Library
  
  


• 
  David
  J. Hodgson, Paul B. Rainey and Angus Buckling, Mechanisms linking
  diversity, productivity and invasibility in experimental bacterial communities, Proceedings of the Royal Society
  of London. Series B: Biological Sciences, 10.1098/rspb.2002.2146, 269, 1506,
  (2277-2283), (2002).
  Crossref
  
  


• 
  David
  Allaway, Neil A. Schofield, Mary E. Leonard, Liliana
  Gilardoni, Turlough M. Finan and Philip S. Poole, Use of differential
  fluorescence induction and optical trapping to isolate environmentally induced genes, Environmental Microbiology, 3,
  6, (397-406), (2001).
  Wiley Online
  Library
  
  


• 
  H.
  Antoun and J. Kloepper, Plant
  Growth Promoting Rhizobacteria (PGPR), Encyclopedia
  of Genetics, 10.1006/rwgn.2001.1636, (1477-1480),
  (2001).
  Crossref
  
  


• 
  E.
  Benizri, E. Baudoin and A.
  Guckert, Root Colonization by Inoculated Plant Growth-Promoting
  Rhizobacteria, Biocontrol
  Science and Technology, 11, 5,
  (557), (2001).
  Crossref
  
  


• 
  Adrian
  J Tett, Thomas R Turner and Philip S Poole, Genomics and the Rhizosphere,
  eLS, (2012).
  Wiley Online Library
  
  


• 
  Ben
  J. J. Lugtenberg, Linda Dekkers and Guido V. Bloemberg, MOLECULARDETERMINANTS
  OFRHIZOSPHERECOLONIZATION BYPSEUDOMONAS, Annual Review of Phytopathology,
  39, 1,
  (461), (2001).
  Crossref
  
  


• 
  Arthur
  H.F Hosie and Philip S Poole,
  Bacterial ABC transporters of amino acids, Research in Microbiology,
  152, 3-4, (259),
  (2001).
  Crossref
  
  


• 
  Guido
  V Bloemberg and Ben J.J Lugtenberg,
  Molecular basis of plant growth promotion and biocontrol by rhizobacteria, Current Opinion in Plant Biology, 4,
  4, (343), (2001).
  Crossref
  
  


• 
  Ultan
  F Walsh, John P Morrissey and Fergal O'Gara, Pseudomonas for biocontrol
  of phytopathogens: from functional genomics to commercial exploitation, Current Opinion in Biotechnology, 12,
  3, (289), (2001).
  Crossref
  
  


• 
  Ezékiel
  Baudoin, Emile Benizri and Armand
  Guckert, Metabolic fingerprint of microbial communities from distinct
  maize rhizosphere compartments, European
  Journal of Soil Biology, 37, 2,
  (85), (2001).
  Crossref
  
  


• 
  Heike
  Schmidt‐Eisenlohr, Michael Rittig, Susanne Preithner and Christian
  Baron, Biomonitoring of pJP4‐carrying Pseudomonas chlororaphis
  with Trb protein‐specific antisera, Environmental
  Microbiology, 3, 11,
  (720-730), (2002).
  Wiley Online
  Library
  
  


• 
  Laurent Noël, Frank
  Thieme, Dirk Nennstiel and Ulla
  Bonas, cDNA‐AFLP analysis unravels a genome‐wide hrpG‐regulon
  in the plant pathogen Xanthomonas campestris pv. vesicatoria,
  Molecular Microbiology,
  41, 6,
  (1271-1281), (2008).
  Wiley Online Library
  
  


• 
  Gail
  M. Preston, Nicolas Bertrand and Paul B. Rainey, Type III secretion
  in plant growth‐promoting Pseudomonas fluorescens SBW25,
  Molecular Microbiology,
  41, 5,
  (999-1014), (2008).
  Wiley Online Library
  
  


• 
  Katarina
  Björklöf and Kirsten S. Jørgensen,
  Applicability of non‐antibiotic resistance marker genes in ecological studies
  of introduced bacteria in forest soil, FEMS Microbiology Ecology,
  38, 2‐3, (179-188),
  (2006).
  Wiley Online Library
  
  


• 
  Gail
  M. Preston, Pseudomonas syringae pv. tomato: the right pathogen,
  of the right plant, at the right time, Molecular Plant Pathology,
  1, 5,
  (263-275), (2001).
  Wiley Online Library
  
  


• 
  Michael
  J. Mahan, Douglas M. Heithoff, Robert L. Sinsheimer and David
  A. Low, Assesment of Bacterial Pathogenesis by Analysis of Gene
  Expression in the Host, Annual
  Review of Genetics, 10.1146/annurev.genet.34.1.139, 34,
  1, (139-164), (2000).
  Crossref
  
  


• 
  J.
  Allan Downie, Siri Ram Chhabra, Andrea Hardman, Yan
  Jiang, Gordon S. A. B. Stewart, Bridget E. Laue, Paul
  Williams, Fergal O’Gara and Sinead Jacob, The biocontrol strain
  Pseudomonas fluorescens F113 produces the Rhizobium small bacteriocin, N-(3-hydroxy-7-cis-tetradecenoyl)homoserine
  lactone, via HdtS, a putative novel N-acylhomoserine lactone synthase, Microbiology, 146,
  10, (2469), (2000).
  Crossref
  
  


• 
  T.M.
  Timms-Wilson, R.J. Ellis and M.J. Bailey, Immuno-capture differential
  display method (IDDM) for the detection of environmentally induced promoters in rhizobacteria, Journal of Microbiological
  Methods, 41, 1,
  (77), (2000).
  Crossref
  
  


• 
  T.
  M. Timms-Wilson, R. J. Ellis, A. Renwick, D.
  J. Rhodes, D. V. Mavrodi, D.
  M. Weller, L. S. Thomashow and M. J. Bailey, Chromosomal Insertion
  of Phenazine-1-Carboxylic Acid Biosynthetic Pathway Enhances Efficacy of Damping-off
  Disease Control byPseudomonas fluorescens, Molecular Plant-Microbe Interactions,
  13, 12,
  (1293), (2000).
  Crossref
  
  


• 
  Paul
  B Rainey and Gail M Preston,
  In vivo expression technology strategies: valuable tools for biotechnology, Current Opinion in Biotechnology, 10.1016/S0958-1669(00)00132-4, 11,
  5, (440-444), (2000).
  Crossref
  
  


• 
  Víctor
  De Lorenzo, Pseudomonas entering the post‐genomic era, Environmental Microbiology, 2,
  3, (349-354), (2001).
  Wiley Online
  Library
  
  


• 
  Michael Givskov, Morten
  Hentzer, Bjarne Kjær Ersbøll, Arne Heydorn, Claus
  Sternberg, Alex Toftgaard Nielsen and Søren Molin, Quantification of biofilm
  structures by the novel computer program comstat, Microbiology, 146, 10,
  (2395), (2000).
  Crossref
  
  


• 
  Douglas
  M. Heithoff, Robert L. Sinsheimer, David A. Low and Michael
  J. Mahan, in vivo gene expression and the adaptive response: from
  pathogenesis to vaccines and antimicrobials, Philosophical Transactions of the Royal Society of London.
  Series B: Biological Sciences, 10.1098/rstb.2000.0604, 355,
  1397, (633-642), (2000).
  Crossref
  
  



• 
  Rosaria
  Campilongo, Rowena K. Y. Fung, Richard H. Little, Lucia
  Grenga, Eleftheria Trampari, Simona Pepe, Govind
  Chandra, Clare E. M. Stevenson, Davide Roncarati and Jacob
  G. Malone, One ligand, two regulators and three binding sites:
  How KDPG controls primary carbon metabolism in Pseudomonas,
  PLOS Genetics,
  10.1371/journal.pgen.1006839,
  13, 6,
  (e1006839), (2017).
  Crossref
  
  



• 
  Mark
  W. Silby and Stuart B. Levy,
  Overlapping Protein-Encoding Genes in Pseudomonas fluorescens Pf0-1, PLoS Genetics, 10.1371/journal.pgen.1000094, 4,
  6, (e1000094), (2008).
  Crossref
  
  



• 
  Alex
  Williams, Pierre Pétriacq, David
  J. Beerling, T. E. Anne Cotton and Jurriaan Ton, Impacts of Atmospheric
  CO2 and Soil Nutritional Value on Plant Responses to Rhizosphere Colonization by Soil
  Bacteria, Frontiers
  in Plant Science, 10.3389/fpls.2018.01493, 9,
  (2018).
  Crossref
  
  



• 
  Nesli
  Tovi, Sammy Frenk, Yitzhak
  Hadar and Dror Minz, Host
  Specificity and Spatial Distribution Preference of Three Pseudomonas Isolates, Frontiers in Microbiology, 10.3389/fmicb.2018.03263, 9,
  (2019).
  Crossref