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. 1998 Dec;180(24):6769–6772. doi: 10.1128/jb.180.24.6769-6772.1998

TABLE 1.

Induction of β-galactosidase expression in P. putida S12(pKRZ-srp) by solvents

Chemical Concn (mM) β-Galactosidase activitya (nmol min−1 mg of protein−1) Induction (fold)
None 3.8 ± 0.1 1.0
Aromatic solvents
 Toluene 1.0 13.3 ± 0.4 3.5
2.0 36.5 ± 0.6 9.6
3.0 48.6 ± 5.4 12.8
4.0 57.0 ± 7.5 15.0
5.0 59.1 ± 3.3 15.6
6.0 64.3 ± 6.6 16.9
 Benzene 3.0 36.6 ± 0.9 9.6
 Styrene 3.0 32.2 ± 3.4 8.5
p-Xylene 3.0 36.0 ± 4.9 9.5
 Ethylbenzene 3.0 47.3 ± 4.1 12.4
 Propylbenzene 3.0 59.0 ± 2.0 15.5
Aliphatic solvents
 Pentane 1.0 30.1 ± 0.8 7.9
 Hexane 1.0 25.2 ± 0.7 6.6
 Heptane 1.0 34.2 ± 1.2 9.0
 Octane 1.0 26.8 ± 0.1 7.1
 Nonane 1.0 23.7 ± 1.0 6.2
Alcohols
 1-Propanol 3.0 22.2 ± 1.2 5.8
 1-Butanol 3.0 25.1 ± 0.5 6.6
 1-Pentanol 3.0 38.1 ± 1.2 10.0
 1-Hexanol 3.0 60.3 ± 2.1 15.9
 1-Heptanol 3.0 66.1 ± 0.2 17.4
 1-Octanol 3.0 46.2 ± 1.2 12.2
a

P. putida S12(pKRZ-srp) cells were grown to late exponential phase (optical density of 1.0 at 600 nm) in LB broth. β-Galactosidase was determined in cell extracts by the method of Miller (16).