CHARACTERIZATION OF A GENOMIC LOCUS REQUIRED FOR SYNTHESIS OF THE ANTIBIOTIC 2,4-DIACETYLPHLOROGLUCINOL BY THE BIOLOGICAL-CONTROL AGENT PSEUDOMONAS-FLUORESCENS Q2-87
Mg. Bangera et Ls. Thomashow, CHARACTERIZATION OF A GENOMIC LOCUS REQUIRED FOR SYNTHESIS OF THE ANTIBIOTIC 2,4-DIACETYLPHLOROGLUCINOL BY THE BIOLOGICAL-CONTROL AGENT PSEUDOMONAS-FLUORESCENS Q2-87, Molecular plant-microbe interactions, 9(2), 1996, pp. 83-90
The antibiotic 2,4-diacetylphloroglucinol (Phl) is an important factor
in the biological control by fluorescent Pseudomonas spp, of many soi
lborne diseases including take-all disease of wheat, A 6.5-kb genomic
DNA fragment from Pseudomonas fluorescens Q2-87 conferred production o
f Phl and of a red pigment distinct from Phl, but which typically is p
resent when Phl is produced, upon all of 13 Phl-nonproducing recipient
Pseudomonas strains into which it was introduced, Larger fragments th
at included flanking DNA sequences did not transfer this capability, s
uggesting that they contain negative regulatory element(s), Analysis o
f the 6.5-kb fragment by Tn3HoHo1 mutagenesis further localized the se
quences required for Phl production to a segment of approximately 5 kb
and revealed the presence of at least two divergently oriented transc
riptional units, Insertions within the smaller unit or within about 3
kb of the 5' end of the larger unit caused loss of production of both
Phl and the red pigment, Other insertions within the distal 1.5 kb of
the larger transcriptional unit abolished production of only the red p
igment, Pleiotropic changes in secondary metabolism or colony morpholo
gy were not observed in Pseudomonas strains containing the 6.5-kb frag
ment, although some Phl-producing derivatives grew more slowly and gav
e rise to smaller colonies than did the wild-type parental strains, Th
e size of the genomic region involved in Phl production, and the consi
stency and specificity with which these sequences transferred Phl bios
ynthetic capability, support the conclusion that the 6.5-kb fragment c
ontains the Phl biosynthetic locus.