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Applied and Environmental Microbiology, September 2006, p. 6079-6087, Vol. 72, No. 9
0099-2240/06/$08.00+0 doi:10.1128/AEM.00559-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
S. Egan,1,2
C. Holmström,1,2
S. James,1,2
H. Lappin-Scott,3 and
S. Kjelleberg1,2*
Centre for Marine Biofouling and Bio-Innovation,1 School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney 2052, New South Wales, Australia,2 Hatherly Laboratories, School of Biosciences, University of Exeter, Exeter, United Kingdom3
Received 8 March 2006/ Accepted 6 July 2006
The marine epiphytic bacterium Pseudoalteromonas tunicata produces a range of extracellular secondary metabolites that inhibit an array of common fouling organisms, including fungi. In this study, we test the hypothesis that the ability to inhibit fungi provides P. tunicata with an advantage during colonization of a surface. Studies on a transposon-generated antifungal-deficient mutant of P. tunicata, FM3, indicated that a long-chain fatty acid-coenzyme A ligase is involved in the production of a broad-range antifungal compound by P. tunicata. Flow cell experiments demonstrated that production of an antifungal compound provided P. tunicata with a competitive advantage against a marine yeast isolate during surface colonization. This compound enabled P. tunicata to disrupt an already established fungal biofilm by decreasing the number of yeast cells attached to the surface by 66% ± 9%. For in vivo experiments, the wild-type and FM3 strains of P. tunicata were used to inoculate the surface of the green alga Ulva australis. Double-gradient denaturing gradient gel electrophoresis analysis revealed that after 48 h, the wild-type P. tunicata had outcompeted the surface-associated fungal community, whereas the antifungal-deficient mutant had no effect on the fungal community. Our data suggest that P. tunicata is an effective competitor against fungal surface communities in the marine environment.
Supplemental material for this article may be found at http://aem.asm.org/.
Present address: The Biomerit Research Centre, Department of Microbiology, National University of Ireland, University College Cork, Cork, Ireland.
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