TABLE 3.
Expt and strain/genotype | Designation | Concn, μg ml−1 (mean ± SEM)b |
|||||
---|---|---|---|---|---|---|---|
2,4-Diacetylphloroglucinol | Monoacetylphloroglucinol | Pyoluteorin | Pyrrolnitrin | Rhizoxin WF-1360F | Orfamide A | ||
1 | |||||||
Pf-5 | JL4585 | 0.10 ± 0.04 | 0.13 ± 0.06 | 8.0 ± 2.1 | 1.2 ± 0.3 | 4.4 ± 0.4 | 100 ± 14 |
ΔprnC | JL4793 | 0.47c | 0.73c | 7.6 ± 0.4 | BD | 5.6 ± 0.7 | 110 ± 14 |
ΔpltA | JL4805 | 7.2 ± 0.4 | 5.6 ± 0.6 | BD | 1.0 ± 0.1 | 8.1 ± 0.4 | 150 ± 3 |
ΔrzxB | JL4808 | 0.04 ± 0.01 | 0.07 ± 0.02 | 8.0 ± 0.7 | 1.1 ± 0.1 | BD | 100 ± 7 |
ΔhcnB | JL4809 | 9.5 ± 0.9 | 12 ± 1 | 11 ± 7 | 1.6 ± 0.3 | 36 ± 11 | 270 ± 20 |
ΔphlA | LK023 | BD | BD | 7.2 ± 1.8 | 1.2 ± 0.2 | 3.8 ± 0.5 | 99 ± 11 |
2 | |||||||
Pf-5 | JL4585 | 0.26 ± 0.15 | 0.65 ± 0.36 | 8.0 ± 0.5 | 1.5 ± 0.1 | 4.5 ± 0.1 | 12 ± 1 |
ΔofaA | JL4807 | 0.03 ± 0.01 | 0.09 ± 0.03 | 7.5 ± 0.6 | 1.6 ± 0.3 | 2.4 ± 0.1 | 0.73 ± 0.01 |
ΔphlA ΔrzxB ΔprnC | LK031 | BD | BD | 8.0 ± 0.1 | BD | BD | 110 ± 2 |
3 | |||||||
Pf-5 | JL4585 | 0.05 ± 0.02 | 0.14 ± 0.1 | 5.9 ± 0.4 | 1.3 ± 0.1 | 3.8 ± 0.1 | 92 ± 1 |
ΔgacA | JL4577 | BD | BD | BD | BD | BD | BD |
ΔphlD | JL4804 | BD | BD | BD | 0.63 ± 0.04 | 4.0 ± 0.2 | 130 ± 7 |
ΔphlD ΔrzxB ΔprnC ΔhcnB ΔpltA ΔofaA ΔtoxB | JL4932 | BD | BD | BD | BD | BD | 0.54 ± 0.11 |
4 | |||||||
Pf-5 | JL4585 | 1.4 ± 0.4 | 2.4 ± 0.6 | 5.5 ± 0.6 | 1.1 ± 0.1 | 5.0 ± 0.1 | 110 ± 7 |
ΔrzxB ΔprnC | JL4902 | 0.30 ± 0.21 | 0.9 ± 0.4 | 6.2 ± 0.6 | BD | BD | 90 ± 1 |
ΔphlA ΔrzxB | LK027 | BD | BD | 5.8 ± 0.1 | 1.2 ± 0.1 | BD | 88 ± 4 |
5 | |||||||
Wild type | JL4585 | 0.16 ± 0.04 | 0.33 ± 0.07 | 4.0 ± 2.9 | 0.70 ± 0.51 | 2.3 ± 1.4 | 56 ± 32 |
ΔphlD ΔprnC | JL4830 | BD | BD | BD | BD | 7.9 ± 0.8 | 130 ± 14 |
ΔphlD ΔrzxB ΔprnC | JL4844 | BD | BD | BD | BD | BD | 130 ± 7 |
ΔphlD ΔrzxB ΔprnC ΔhcnB ΔpltA | JL4865 | BD | BD | BD | BD | BD | 300 ± 1 |
ΔphlD ΔrzxB | JL4901 | BD | BD | BD | 1.0 ± 0.1 | BD | 120 ± 1 |
P. protegens Pf-5 or derivative strains were grown in 5 ml of NYBGly supplemented with 0.35 mM zinc sulfate (NYBGly-Zn). Cultures were incubated for 48 h at 20°C with shaking at 200 rpm before the concentrations of the antibiotics were quantified by HPLC.
The values represent the mean and standard error of the mean for two replicates, each composed of four broth cultures. Values were rounded to two significant digits. BD, below detection, with detection limits being approximately 0.02 μg ml−1 for each compound.
The compound was detected in only one of the two replicates. The value shown is one half the concentration determined from the replicate in which the compound was detected.