Previous Article | Next Article ![]()
Appl. Environ. Microbiol., Nov 1997, 4340-4345, Vol 63, No. 11
A Gaballa, PD Abeysinghe, G Urich, S Matthijs, H De Greve, P Cornelis and N Koedam
Pseudomonas fluorescens ATCC 17400 shows in vitro activity against Pythium
debaryanum under conditions of iron limitation. A lacZ reporter gene
introduced by transposon mutagenesis into the P. fluorescens ATCC 17400
trehalase gene (treA) was induced by a factor released by the phytopathogen
Pythium debaryanum. The induction of the lacZ gene was lost upon treatment
of the Pythium supernatant with commercial trehalase. A trehalose
concentration as low as 1 microM could induce the expression of treA. The
mutation did not affect the wild-type potential for fungus antagonism but
drastically decreased the osmotolerance of the mutant in liquid culture and
suppressed the ability of P. fluorescens ATCC 17400 to utilize trehalose as
a carbon source. A subsequent transposon insertion in treP, one of the
trehalose phosphotransferase genes upstream of treA, silenced the lacZ
gene. This double mutant restricted fungal growth only under conditions of
high osmolarity, which probably results in internal trehalose accumulation.
These data confirm the role of the disaccharide trehalose in osmotolerance,
and they indicate its additional role as an initiator of or a signal for
fungal antagonism.
Copyright © 1997, American Society for Microbiology
Trehalose induces antagonism towards Pythium debaryanum in Pseudomonas fluorescens ATCC 17400
Laboratorium Plantenfysiologie, Flanders Interuniversity Institute for Biotechnology, Vrije Universiteit Brussel, Belgium.
This article has been cited by other articles:
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»