Microbiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Microbiology 150 (2004), 3405-3413; DOI  10.1099/mic.0.27357-0
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
Right arrow Citation Map
Services
Right arrow Email this article to a friend
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 arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Pham, T. H.
Right arrow Articles by Rehm, B. H. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Pham, T. H.
Right arrow Articles by Rehm, B. H. A.
Agricola
Right arrow Articles by Pham, T. H.
Right arrow Articles by Rehm, B. H. A.
Microbiology 150 (2004), 3405-3413; DOI  10.1099/mic.0.27357-0
© 2004 Society for General Microbiology

The role of polyhydroxyalkanoate biosynthesis by Pseudomonas aeruginosa in rhamnolipid and alginate production as well as stress tolerance and biofilm formation

Thi Hang Pham1, Jeremy S. Webb2 and Bernd H. A. Rehm3

1 Institut für Molekulare Mikrobiologie and Biotechnologie, Westfälische Wilhelms-Universität Münster, Corrensstrasse 3, D-48149 Münster, Germany
2 School of Biotechnology and Biomolecular Sciences and Centre for Marine Biofouling and Bioinnovation, University of New South Wales, NSW 2052, Sydney, Australia
3 Institute of Molecular Biosciences, Massey University, Private Bag 11222, Palmerston North, New Zealand

Correspondence
Bernd H. A. Rehm
B.Rehm{at}massey.ac.nz

Pseudomonas aeruginosa is capable of synthesizing polyhydroxyalkanoic acids (PHAs) and rhamnolipids, both of which are composed of 3-hydroxydecanoic acids connected by ester bonds, as well as synthesizing the biofilm matrix polymer alginate. In order to study the influence of PHA biosynthesis on rhamnolipid and alginate biosynthesis, as well as stress tolerance and biofilm formation, isogenic knock-out mutants deficient in PHA biosynthesis were generated for P. aeruginosa PAO1 and the alginate-overproducing P. aeruginosa FRD1. A gentamicin-resistance cassette was inserted replacing the 3' region of phaC1, the whole of phaZ and the 5' region of phaC2. Gas chromatography/mass spectrometry analysis showed that PHA accumulation was completely abolished in both strains. Interestingly, this gene replacement did not abolish rhamnolipid production. Thus, as previously suggested, the PHA synthase is not directly involved in rhamnolipid biosynthesis. In the PHA-negative mutant of mucoid FRD1 alginate biosynthesis was not affected, whereas in the PHA-negative PAO1 mutant an almost threefold increase in biosynthesis was observed compared to the wild-type. Consistently, PHA accumulation in FRD1 contributed only 4·7 % of cell dry weight, which is fourfold less than in PAO1. These data suggest that PHA biosynthesis and alginate biosynthesis are in competition with respect to a common precursor. The surface attachment and biofilm development of the PHA-negative mutants were also compared to those of wild-type strains in glass flow-cell reactors. PHA-negative mutants of P. aeruginosa PAO1 and FRD1 showed reduced attachment to glass. However, the PAO1 PHA-negative mutant, in contrast to the wild-type, formed a stable biofilm with large, distinct and differentiated microcolonies characteristic of alginate-overproducing strains of P. aeruginosa. The stress tolerance of PHA-negative mutants with respect to elevated temperature was strongly impaired. These data indicated a functional role for PHA in stress response and tolerance.


Abbreviations: ACP, acyl carrier priotein; CDW, cell dry weight; CLSM, confocal laser scanning microscope; MCL, medium chain length; PHA, polyhydroxyalkanoic acid; Rt, rhamnosyltransferase




This article has been cited by other articles:


Home page
MicrobiologyHome page
T. L. Lindsey, J. M. Hagins, P. A. Sokol, and L. A. Silo-Suh
Virulence determinants from a cystic fibrosis isolate of Pseudomonas aeruginosa include isocitrate lyase
Microbiology, June 1, 2008; 154(6): 1616 - 1627.
[Abstract] [Full Text] [PDF]


Home page
MicrobiologyHome page
T. Hindre, H. Bruggemann, C. Buchrieser, and Y. Hechard
Transcriptional profiling of Legionella pneumophila biofilm cells and the influence of iron on biofilm formation
Microbiology, January 1, 2008; 154(1): 30 - 41.
[Abstract] [Full Text] [PDF]


Home page
Appl. Environ. Microbiol.Home page
A. Campisano, C. Schroeder, M. Schemionek, J. Overhage, and B. H. A. Rehm
PslD Is a Secreted Protein Required for Biofilm Formation by Pseudomonas aeruginosa
Appl. Envir. Microbiol., April 1, 2006; 72(4): 3066 - 3068.
[Abstract] [Full Text] [PDF]


Home page
Appl. Environ. Microbiol.Home page
V. Peters and B. H. A. Rehm
In vivo enzyme immobilization by use of engineered polyhydroxyalkanoate synthase.
Appl. Envir. Microbiol., March 1, 2006; 72(3): 1777 - 1783.
[Abstract] [Full Text] [PDF]


Home page
Appl. Environ. Microbiol.Home page
J. Overhage, M. Schemionek, J. S. Webb, and B. H. A. Rehm
Expression of the psl Operon in Pseudomonas aeruginosa PAO1 Biofilms: PslA Performs an Essential Function in Biofilm Formation
Appl. Envir. Microbiol., August 1, 2005; 71(8): 4407 - 4413.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 2004 Society for General Microbiology.