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Journal Abstract Search

179 related items for PubMed ID: 21091602

  • 1. In silico analysis reveals multiple putative type VI secretion systems and effector proteins in Pseudomonas syringae pathovars.
    Sarris PF, Skandalis N, Kokkinidis M, Panopoulos NJ.
    Mol Plant Pathol; 2010 Nov; 11(6):795-804. PubMed ID: 21091602
    [Abstract] [Full Text] [Related]

  • 2. Contributions of the effector gene hopQ1-1 to differences in host range between Pseudomonas syringae pv. phaseolicola and P. syringae pv. tabaci.
    Ferrante P, Clarke CR, Cavanaugh KA, Michelmore RW, Buonaurio R, Vinatzer BA.
    Mol Plant Pathol; 2009 Nov; 10(6):837-42. PubMed ID: 19849789
    [Abstract] [Full Text] [Related]

  • 3. Pseudomonas syringae pv. tomato DC3000 uses constitutive and apoplast-induced nutrient assimilation pathways to catabolize nutrients that are abundant in the tomato apoplast.
    Rico A, Preston GM.
    Mol Plant Microbe Interact; 2008 Feb; 21(2):269-82. PubMed ID: 18184070
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  • 4. Whole-genome sequence analysis of Pseudomonas syringae pv. phaseolicola 1448A reveals divergence among pathovars in genes involved in virulence and transposition.
    Joardar V, Lindeberg M, Jackson RW, Selengut J, Dodson R, Brinkac LM, Daugherty SC, Deboy R, Durkin AS, Giglio MG, Madupu R, Nelson WC, Rosovitz MJ, Sullivan S, Crabtree J, Creasy T, Davidsen T, Haft DH, Zafar N, Zhou L, Halpin R, Holley T, Khouri H, Feldblyum T, White O, Fraser CM, Chatterjee AK, Cartinhour S, Schneider DJ, Mansfield J, Collmer A, Buell CR.
    J Bacteriol; 2005 Sep; 187(18):6488-98. PubMed ID: 16159782
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  • 5. A draft genome sequence of Pseudomonas syringae pv. tomato T1 reveals a type III effector repertoire significantly divergent from that of Pseudomonas syringae pv. tomato DC3000.
    Almeida NF, Yan S, Lindeberg M, Studholme DJ, Schneider DJ, Condon B, Liu H, Viana CJ, Warren A, Evans C, Kemen E, Maclean D, Angot A, Martin GB, Jones JD, Collmer A, Setubal JC, Vinatzer BA.
    Mol Plant Microbe Interact; 2009 Jan; 22(1):52-62. PubMed ID: 19061402
    [Abstract] [Full Text] [Related]

  • 6. HSI-II Gene Cluster of Pseudomonas syringae pv. tomato DC3000 Encodes a Functional Type VI Secretion System Required for Interbacterial Competition.
    Chien CF, Liu CY, Lu YY, Sung YH, Chen KY, Lin NC.
    Front Microbiol; 2020 Jan; 11():1118. PubMed ID: 32582082
    [Abstract] [Full Text] [Related]

  • 7. The Erwinia amylovora avrRpt2EA gene contributes to virulence on pear and AvrRpt2EA is recognized by Arabidopsis RPS2 when expressed in pseudomonas syringae.
    Zhao Y, He SY, Sundin GW.
    Mol Plant Microbe Interact; 2006 Jun; 19(6):644-54. PubMed ID: 16776298
    [Abstract] [Full Text] [Related]

  • 8. Closing the circle on the discovery of genes encoding Hrp regulon members and type III secretion system effectors in the genomes of three model Pseudomonas syringae strains.
    Lindeberg M, Cartinhour S, Myers CR, Schechter LM, Schneider DJ, Collmer A.
    Mol Plant Microbe Interact; 2006 Nov; 19(11):1151-8. PubMed ID: 17073298
    [Abstract] [Full Text] [Related]

  • 9. Pseudomonas syringae exchangeable effector loci: sequence diversity in representative pathovars and virulence function in P. syringae pv. syringae B728a.
    Deng WL, Rehm AH, Charkowski AO, Rojas CM, Collmer A.
    J Bacteriol; 2003 Apr; 185(8):2592-602. PubMed ID: 12670984
    [Abstract] [Full Text] [Related]

  • 10. Bioinformatics-enabled identification of the HrpL regulon and type III secretion system effector proteins of Pseudomonas syringae pv. phaseolicola 1448A.
    Vencato M, Tian F, Alfano JR, Buell CR, Cartinhour S, DeClerck GA, Guttman DS, Stavrinides J, Joardar V, Lindeberg M, Bronstein PA, Mansfield JW, Myers CR, Collmer A, Schneider DJ.
    Mol Plant Microbe Interact; 2006 Nov; 19(11):1193-206. PubMed ID: 17073302
    [Abstract] [Full Text] [Related]

  • 11. The hrpK operon of Pseudomonas syringae pv. tomato DC3000 encodes two proteins secreted by the type III (Hrp) protein secretion system: HopB1 and HrpK, a putative type III translocator.
    Petnicki-Ocwieja T, van Dijk K, Alfano JR.
    J Bacteriol; 2005 Jan; 187(2):649-63. PubMed ID: 15629936
    [Abstract] [Full Text] [Related]

  • 12. Type IV pilin is glycosylated in Pseudomonas syringae pv. tabaci 6605 and is required for surface motility and virulence.
    Nguyen LC, Taguchi F, Tran QM, Naito K, Yamamoto M, Ohnishi-Kameyama M, Ono H, Yoshida M, Chiku K, Ishii T, Inagaki Y, Toyoda K, Shiraishi T, Ichinose Y.
    Mol Plant Pathol; 2012 Sep; 13(7):764-74. PubMed ID: 22353307
    [Abstract] [Full Text] [Related]

  • 13. Housekeeping gene sequencing and multilocus variable-number tandem-repeat analysis to identify subpopulations within Pseudomonas syringae pv. maculicola and Pseudomonas syringae pv. tomato that correlate with host specificity.
    Gironde S, Manceau C.
    Appl Environ Microbiol; 2012 May; 78(9):3266-79. PubMed ID: 22389364
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  • 18. Pseudomonas syringae pv. tomato DC3000 type III effector HopAA1-1 functions redundantly with chlorosis-promoting factor PSPTO4723 to produce bacterial speck lesions in host tomato.
    Munkvold KR, Russell AB, Kvitko BH, Collmer A.
    Mol Plant Microbe Interact; 2009 Nov; 22(11):1341-55. PubMed ID: 19810804
    [Abstract] [Full Text] [Related]

  • 19. Characterization of the osmoprotectant transporter OpuC from Pseudomonas syringae and demonstration that cystathionine-beta-synthase domains are required for its osmoregulatory function.
    Chen C, Beattie GA.
    J Bacteriol; 2007 Oct; 189(19):6901-12. PubMed ID: 17660277
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  • 20. Characterization of the PvdS-regulated promoter motif in Pseudomonas syringae pv. tomato DC3000 reveals regulon members and insights regarding PvdS function in other pseudomonads.
    Swingle B, Thete D, Moll M, Myers CR, Schneider DJ, Cartinhour S.
    Mol Microbiol; 2008 May; 68(4):871-89. PubMed ID: 18363796
    [Abstract] [Full Text] [Related]

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