Exploitation of gene(s) involved in 2,4-diacetylphloroglucinol biosynthesis to confer a new biocontrol capability to a Pseudomonas strain

Tn5 mutagenesis and complementation analysis were used to clone a 6-kb genomic fragment required for biosynthesis of 2,4-diacetylphloroglucinol (Phl) from fluorescent Pseudomonas sp. strain F113. A recombinant plasmid, pCU203, containing this region partially complemented a Phl production-negative m...

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Published inApplied and Environmental Microbiology Vol. 58; no. 12; pp. 3873 - 3878
Main Authors Fenton, A.M. (University College, Cork, Ireland), Stephens, P.M, Crowley, J, O'Callaghan, M, O'Gara, F
Format Journal Article
LanguageEnglish
Published Washington, DC American Society for Microbiology 01.12.1992
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Abstract Tn5 mutagenesis and complementation analysis were used to clone a 6-kb genomic fragment required for biosynthesis of 2,4-diacetylphloroglucinol (Phl) from fluorescent Pseudomonas sp. strain F113. A recombinant plasmid, pCU203, containing this region partially complemented a Phl production-negative mutant (F113G22) derived from strain F113. When sugar beet seeds were sown into an unsterilized soil, in which sugar beet was subject to damping-off by Pythium ultimum, the emergence of sugar beet seeds inoculated with strain F113 was significantly greater than that of seeds inoculated with F113G22. Transfer of pCU203 into eight other Pseudomonas strains conferred the ability to synthesize Phi in only one of these strains, Pseudomonas sp. strain M114. Strain M114(pCU203) showed enhanced antagonism towards P. ultimum in vitro and significantly increased the emergence of sugar beet seeds in the same soil compared with emergence induced by the parent strain M114
AbstractList Tn5 mutagenesis and complementation analysis were used to clone a 6-kb genomic fragment required for biosynthesis of 2,4-diacetylphloroglucinol (Phl) from fluorescent Pseudomonas sp. strain F113. A recombinant plasmid, pCU203, containing this region partially complemented a Phl production-negative mutant (F113G22) derived from strain F113. When sugar beet seeds were sown into an unsterilized soil, in which sugar beet was subject to damping-off by Pythium ultimum, the emergence of sugar beet seeds inoculated with strain F113 was significantly greater than that of seeds inoculated with F113G22. Transfer of pCU203 into eight other Pseudomonas strains conferred the ability to synthesize Phl in only one of these strains, Pseudomonas sp. strain M114. Strain M114(pCU203) showed enhanced antagonism towards P. ultimum in vitro and significantly increased the emergence of sugar beet seeds in the same soil compared with emergence induced by the parent strain M114.
Tn5 mutagenesis and complementation analysis were used to clone a 6-kb genomic fragment required for biosynthesis of 2,4-diacetylphloroglucinol (Phl) from fluorescent Pseudomonas sp. strain F113. A recombinant plasmid, pCU203, containing this region partially complemented a Phl production-negative mutant (F113G22) derived from strain F113. When sugar beet seeds were sown into an unsterilized soil, in which sugar beet was subject to damping-off by Pythium ultimum, the emergence of sugar beet seeds inoculated with strain F113 was significantly greater than that of seeds inoculated with F113G22. Transfer of pCU203 into eight other Pseudomonas strains conferred the ability to synthesize Phi in only one of these strains, Pseudomonas sp. strain M114. Strain M114(pCU203) showed enhanced antagonism towards P. ultimum in vitro and significantly increased the emergence of sugar beet seeds in the same soil compared with emergence induced by the parent strain M114
Tn5 mutagenesis and complementation analysis were used to clone a 6-kb genomic fragment required for biosynthesis of 2,4-diacetylphloroglucinol (Phl) from fluorescent Pseudomonas sp. strain F113. A recombinant plasmid, pCU203, containing this region partially complemented a Phl production-negative mutant (F113G22) derived from strain F113. When sugar beet seeds were sown into an unsterilized soil, in which sugar beet was subject to damping-off by Pythium ultimum, the emergence of sugar beet seeds inoculated with strain F113 was significantly greater than that of seeds inoculated with F113G22. Transfer of pCU203 into eight other Pseudomonas strains conferred the ability to synthesize Phi in only one of these strains, Pseudomonas sp. strain M114. Strain M114(pCU203) showed enhanced antagonism towards P. ultimum in vitro and significantly increased the emergence of sugar beet seeds in the same soil compared with emergence induced by the parent strain M114.
Tn5 mutagenesis and complementation analysis were used to clone a 6-kb genomic fragment required for biosynthesis of 2,4-diacetylphloroglucinol (Phl) from fluorescent Pseudomonas sp. strain F113. A recombinant plasmid, pCU203, containing this region partially complemented a Phl production-negative mutant (F113G22) derived from strain F113. When sugar beet seeds were sown into an unsterilized soil, in which sugar beet was subject to damping-off by Pythium ultimum, the emergence of sugar beet seeds inoculated with strain F113 was significantly greater than that of seeds inoculated with F113G22. Transfer of pCU203 into eight other Pseudomonas strains conferred the ability to synthesize Phl in only one of these strains, Pseudomonas sp. strain M114. Strain M114(pCU203) showed enhanced antagonism towards P. ultimum in vitro and significantly increased the emergence of sugar beet seeds in the same soil compared with emergence induced by the parent strain M114.Tn5 mutagenesis and complementation analysis were used to clone a 6-kb genomic fragment required for biosynthesis of 2,4-diacetylphloroglucinol (Phl) from fluorescent Pseudomonas sp. strain F113. A recombinant plasmid, pCU203, containing this region partially complemented a Phl production-negative mutant (F113G22) derived from strain F113. When sugar beet seeds were sown into an unsterilized soil, in which sugar beet was subject to damping-off by Pythium ultimum, the emergence of sugar beet seeds inoculated with strain F113 was significantly greater than that of seeds inoculated with F113G22. Transfer of pCU203 into eight other Pseudomonas strains conferred the ability to synthesize Phl in only one of these strains, Pseudomonas sp. strain M114. Strain M114(pCU203) showed enhanced antagonism towards P. ultimum in vitro and significantly increased the emergence of sugar beet seeds in the same soil compared with emergence induced by the parent strain M114.
Tn5 mutagenesis and complementation analysis were used to clone a 6-kb genomic fragment required for biosynthesis of 2,4-diacetylphloroglucinol (Phl) from fluorescent Pseudomonas sp. strain F113. A recombinant plasmid, pCU203, containing this region partially complemented a Phl production-negative mutant (F113G22) derived from strain F113. When sugar beet seeds were sown into an unsterilized soil, in which sugar beet was subject to damping-off by Pythium ultimum , the emergence of sugar beet seeds inoculated with strain F113 was significantly greater that that of seeds inoculated with F113G22. Transfer of pCU203 into eight other Pseudomonas strains conferred the ability to synthesize Phl in only one of these strains, Pseudomonas sp. strain M114. Strain M114 (pCu203) showed enhanced antagonism toward P. ultimum in vitro and significantly increased the emergence of sugar beet seeds in the same soil compared with emergence induced by the parent strain M114.
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Tn5 mutagenesis and complementation analysis were used to clone a 6-kb genomic fragment required for biosynthesis of 2,4-diacetylphloroglucinol from fluorescent Pseudomonas sp. strain F113. When sugar beet seeds were sown into unsterilized soil, the emergence of sugar beet seeds inoculated with strain F113 was significantly greater than that of seeds inoculated with F113G22.
Author Crowley, J
Fenton, A.M. (University College, Cork, Ireland)
Stephens, P.M
O'Callaghan, M
O'Gara, F
AuthorAffiliation Department of Microbiology, University College, Cork, Ireland
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Issue 12
Keywords Pseudomonadales
Genetic transformation
Phycomycetes
Biosynthesis
Pseudomonas
Fungi
Rhizosphere
Antagonism
Pythium ultimum
Gene
Mutagenesis
Bacteria
Pseudomonadaceae
Sugar beet
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Thallophyta
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References 2826392 - J Bacteriol. 1988 Jan;170(1):163-70
388356 - Nucleic Acids Res. 1979 Nov 24;7(6):1513-23
2121587 - FEMS Microbiol Lett. 1990 Jul;58(2):221-5
16348176 - Appl Environ Microbiol. 1990 Apr;56(4):908-12
16348633 - Appl Environ Microbiol. 1992 Jan;58(1):353-8
2841289 - J Bacteriol. 1988 Aug;170(8):3499-508
1660695 - Appl Environ Microbiol. 1991 Oct;57(10):2928-34
3005234 - J Bacteriol. 1986 Mar;165(3):696-703
13184240 - J Lab Clin Med. 1954 Aug;44(2):301-7
4202995 - J Bacteriol. 1974 Jan;117(1):283-9
References_xml – reference: 4202995 - J Bacteriol. 1974 Jan;117(1):283-9
– reference: 2841289 - J Bacteriol. 1988 Aug;170(8):3499-508
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– reference: 388356 - Nucleic Acids Res. 1979 Nov 24;7(6):1513-23
– reference: 2826392 - J Bacteriol. 1988 Jan;170(1):163-70
– reference: 16348633 - Appl Environ Microbiol. 1992 Jan;58(1):353-8
– reference: 16348176 - Appl Environ Microbiol. 1990 Apr;56(4):908-12
– reference: 2121587 - FEMS Microbiol Lett. 1990 Jul;58(2):221-5
– reference: 13184240 - J Lab Clin Med. 1954 Aug;44(2):301-7
– reference: 1660695 - Appl Environ Microbiol. 1991 Oct;57(10):2928-34
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Snippet Tn5 mutagenesis and complementation analysis were used to clone a 6-kb genomic fragment required for biosynthesis of 2,4-diacetylphloroglucinol (Phl) from...
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Tn5 mutagenesis and complementation analysis were used to clone a 6-kb genomic fragment required for biosynthesis of 2,4-diacetylphloroglucinol from...
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StartPage 3873
SubjectTerms analogs & derivatives
Anti-Bacterial Agents
Anti-Bacterial Agents - metabolism
ANTIBIOTICOS
antibiotics
ANTIBIOTIQUE
BETA VULGARIS
Biological and medical sciences
Biological control
Biology of microorganisms of confirmed or potential industrial interest
BIOSINTESIS
BIOSYNTHESE
Biosynthesis
Biotechnology
CONTROL BIOLOGICO
CONTROL DE ENFERMEDADES
CONTROLE DE MALADIES
disease control
Fundamental and applied biological sciences. Psychology
GENE
Gene Expression
GENES
Genes, Bacterial
Genetics
GRAINE
LUTTE BIOLOGIQUE
metabolism
microbiology
Mission oriented research
Phloroglucinol
Phloroglucinol - analogs & derivatives
Phloroglucinol - metabolism
plant diseases and disorders
Plants
Plants - microbiology
PSEUDOMONAS
Pseudomonas - genetics
Pseudomonas - metabolism
PYTHIUM ULTIMUM
seeds
SEMILLA
Sugar
Vegetables
Title Exploitation of gene(s) involved in 2,4-diacetylphloroglucinol biosynthesis to confer a new biocontrol capability to a Pseudomonas strain
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