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. 2002 May;68(5):2229–2235. doi: 10.1128/AEM.68.5.2229-2235.2002

TABLE 2.

Influence of F. oxysporum culture filtrates on phlA expression in P. fluorescens CHA0 and CHA638a

P. fluorescens strain F. oxysporum strain FA concn in bacterial growth medium (μM) β-Galactosidase activity (U per 108 CFU)
OD600 = 1.5 OD600 = 2.5
CHA0 None 0 1,510 a 2,100 a
240 0 1,520 a 2,000 a
241 25 1,480 a 1,910 a
242 0 1,460 a 1,950 a
410 0 1,640 a 1,920 a
798 700 220 b 590 b
801 160 200 b 1,520 c
CHA638 None 0 1,850 a 1,720 a
240 0 1,660 a 1,390 a
241 25 1,590 a 1,590 a
242 0 1,540 a 1,560 a
410 0 1,740 a 1,680 a
798 700 1,660 a 1,490 a
801 160 1,680 a 1,470 a
a

P. fluorescens CHA0 (wild type) and CHA638 (phlF mutant) carrying a translational phlA′-′lacZ fusion on plasmid pME6259 were tested. The F. oxysporum strains were cultivated in Czapek Dox medium for 7 days at 24°C and 180 rpm. Filtrates from F. oxysporum cultures were added to bacterial growth medium OSG at a ratio of 20% (vol/vol). The FA content of the culture filtrates was determined, and the final FA concentration in the bacterial growth medium is indicated. β-Galactosidase activities were determined in bacterial cultures grown to an OD600 of 1.5 ± 0.1 or 2.5 ± 0.1, as indicated. Data represent means of three replicate cultures. Means for the same P. fluorescens strain within a column followed by a different letter are significantly different at P ≤ 0.05 according to Fisher's protected least significant difference test.