This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Keith, L. M. W.
Right arrow Articles by Bender, C. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Keith, L. M. W.
Right arrow Articles by Bender, C. L.

 Previous Article  |  Next Article 

Journal of Bacteriology, December 1999, p. 7176-7184, Vol. 181, No. 23
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

AlgT (sigma 22) Controls Alginate Production and Tolerance to Environmental Stress in Pseudomonas syringae

Lisa M. W. Keith and Carol L. Bender*

Department of Entomology and Plant Pathology, Oklahoma State University, Stillwater, Oklahoma 74078

Received 20 July 1999/Accepted 17 September 1999

Pseudomonas aeruginosa and the phytopathogen P. syringae produce the exopolysaccharide alginate, which is a copolymer of D-mannuronic and L-guluronic acids. One of the key regulatory genes controlling alginate biosynthesis in P. aeruginosa is algT, which encodes the alternate sigma factor, sigma 22. In the present study, the algT gene product from P. syringae pv. syringae showed 90% amino acid identity with its P. aeruginosa counterpart, and sequence analysis of the region flanking algT in P. syringae revealed the presence of nadB, mucA, and mucB in an arrangement virtually identical to that of P. aeruginosa. An algT mutant of P. syringae was defective in alginate production but could be complemented with wild-type algT from P. syringae or P. aeruginosa when expressed in trans. The algT mutant also displayed increased sensitivity to heat, paraquat, and hydrogen peroxide (H2O2); the latter two compounds are known to generate reactive oxygen intermediates. Signals for activation of algT gene expression in P. syringae were investigated with an algT::uidA transcriptional fusion. Like that in P. aeruginosa, algT transcription in P. syringae was activated by heat shock. However, algT expression in P. syringae was also stimulated by osmotic stress and by exposure to paraquat, H2O2, and copper sulfate. The latter two compounds are frequently encountered during colonization of plant tissue and may be unique signals for algT activation in P. syringae.


* Corresponding author. Mailing address: 110 Noble Research Center, Department of Entomology and Plant Pathology, Oklahoma State University, Stillwater, OK 74078-3032. Phone: (405) 744-9945. Fax: (405) 744-7373. E-mail: cbender{at}okstate.edu.


Journal of Bacteriology, December 1999, p. 7176-7184, Vol. 181, No. 23
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Schenk, A., Weingart, H., Ullrich, M. S. (2008). The alternative sigma factor AlgT, but not alginate synthesis, promotes in planta multiplication of Pseudomonas syringae pv. glycinea. Microbiology 154: 413-421 [Abstract] [Full Text]  
  • Chang, W.-S., van de Mortel, M., Nielsen, L., Nino de Guzman, G., Li, X., Halverson, L. J. (2007). Alginate Production by Pseudomonas putida Creates a Hydrated Microenvironment and Contributes to Biofilm Architecture and Stress Tolerance under Water-Limiting Conditions. J. Bacteriol. 189: 8290-8299 [Abstract] [Full Text]  
  • da Silva Neto, J. F., Koide, T., Gomes, S. L., Marques, M. V. (2007). The Single Extracytoplasmic-Function Sigma Factor of Xylella fastidiosa Is Involved in the Heat Shock Response and Presents an Unusual Regulatory Mechanism. J. Bacteriol. 189: 551-560 [Abstract] [Full Text]  
  • Taguchi, F., Ogawa, Y., Takeuchi, K., Suzuki, T., Toyoda, K., Shiraishi, T., Ichinose, Y. (2006). A Homologue of the 3-Oxoacyl-(Acyl Carrier Protein) Synthase III Gene Located in the Glycosylation Island of Pseudomonas syringae pv. tabaci Regulates Virulence Factors via N-Acyl Homoserine Lactone and Fatty Acid Synthesis. J. Bacteriol. 188: 8376-8384 [Abstract] [Full Text]  
  • Schenk, A., Berger, M., Keith, L. M., Bender, C. L., Muskhelishvili, G., Ullrich, M. S. (2006). The algT Gene of Pseudomonas syringae pv. glycinea and New Insights into the Transcriptional Organization of the algT-muc Gene Cluster. J. Bacteriol. 188: 8013-8021 [Abstract] [Full Text]  
  • Soto, M. J., Sanjuan, J., Olivares, J. (2006). Rhizobia and plant-pathogenic bacteria: common infection weapons.. Microbiology 152: 3167-3174 [Abstract] [Full Text]  
  • Gourion, B., Rossignol, M., Vorholt, J. A. (2006). A proteomic study of Methylobacterium extorquens reveals a response regulator essential for epiphytic growth. Proc. Natl. Acad. Sci. USA 103: 13186-13191 [Abstract] [Full Text]  
  • Wang, N., Lu, S.-E., Records, A. R., Gross, D. C. (2006). Characterization of the Transcriptional Activators SalA and SyrF, Which Are Required for Syringomycin and Syringopeptin Production by Pseudomonas syringae pv. syringae. J. Bacteriol. 188: 3290-3298 [Abstract] [Full Text]  
  • Sadovskaya, I., Vinogradov, E., Flahaut, S., Kogan, G., Jabbouri, S. (2005). Extracellular Carbohydrate-Containing Polymers of a Model Biofilm-Producing Strain, Staphylococcus epidermidis RP62A. Infect. Immun. 73: 3007-3017 [Abstract] [Full Text]  
  • Kaufusi, P. H., Forsberg, L. S., Tittabutr, P., Borthakur, D. (2004). Regulation of exopolysaccharide synthesis in Rhizobium sp. strain TAL1145 involves an alternative sigma factor gene, rpoH2. Microbiology 150: 3473-3482 [Abstract] [Full Text]  
  • Penaloza-Vazquez, A., Fakhr, M. K., Bailey, A. M., Bender, C. L. (2004). AlgR functions in algC expression and virulence in Pseudomonas syringae pv. syringae. Microbiology 150: 2727-2737 [Abstract] [Full Text]  
  • de Pinto, M. C., Lavermicocca, P., Evidente, A., Corsaro, M. M., Lazzaroni, S., De Gara, L. (2003). Exopolysaccharides Produced by Plant Pathogenic Bacteria Affect Ascorbate Metabolism in Nicotiana tabacum. Plant Cell Physiol 44: 803-810 [Abstract] [Full Text]  
  • Leverrier, P., Dimova, D., Pichereau, V., Auffray, Y., Boyaval, P., Jan, G. (2003). Susceptibility and Adaptive Response to Bile Salts in Propionibacterium freudenreichii: Physiological and Proteomic Analysis. Appl. Environ. Microbiol. 69: 3809-3818 [Abstract] [Full Text]  
  • Keith, R. C., Keith, L. M. W., Hernandez-Guzman, G., Uppalapati, S. R., Bender, C. L. (2003). Alginate gene expression by Pseudomonas syringae pv. tomato DC3000 in host and non-host plants. Microbiology 149: 1127-1138 [Abstract] [Full Text]  
  • Lindow, S. E., Brandl, M. T. (2003). Microbiology of the Phyllosphere. Appl. Environ. Microbiol. 69: 1875-1883 [Full Text]  
  • Mascher, F., Moenne-Loccoz, Y., Schnider-Keel, U., Keel, C., Haas, D., Defago, G. (2002). Inactivation of the Regulatory Gene algU or gacA Can Affect the Ability of Biocontrol Pseudomonas fluorescens CHA0 To Persist as Culturable Cells in Nonsterile Soil. Appl. Environ. Microbiol. 68: 2085-2088 [Abstract] [Full Text]  
  • Schnider-Keel, U., Lejbolle, K. B., Baehler, E., Haas, D., Keel, C. (2001). The Sigma Factor AlgU (AlgT) Controls Exopolysaccharide Production and Tolerance towards Desiccation and Osmotic Stress in the Biocontrol Agent Pseudomonas fluorescens CHA0. Appl. Environ. Microbiol. 67: 5683-5693 [Abstract] [Full Text]  
  • Willis, D. K., Holmstadt, J. J., Kinscherf, T. G. (2001). Genetic Evidence that Loss of Virulence Associated with gacS or gacA Mutations in Pseudomonas syringae B728a Does Not Result from Effects on Alginate Production. Appl. Environ. Microbiol. 67: 1400-1403 [Abstract] [Full Text]  
  • Hild, E., Takayama, K., Olsson, R.-M., Kjelleberg, S. (2000). Evidence for a Role of rpoE in Stressed and Unstressed Cells of Marine Vibrio angustum Strain S14. J. Bacteriol. 182: 6964-6974 [Abstract] [Full Text]  
  • Núñez, C., León, R., Guzmán, J., Espín, G., Soberón-Chávez, G. (2000). Role of Azotobacter vinelandii mucA and mucC Gene Products in Alginate Production. J. Bacteriol. 182: 6550-6556 [Abstract] [Full Text]