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. 1998 May;180(10):2660–2669. doi: 10.1128/jb.180.10.2660-2669.1998

TABLE 4.

Stress and analog induction of dctAp

Strain Genotype β-Galactosidase activity under the following growth conditiona:
Glc-10 mM NH4 Glc-0.5 mM NH4 Glc-NH450 mM sucrose Glc-NH4100 mM sucrose Glc-NH4itaconic acid Glc–NH4– Me-Succ Glc–NH4– DiMe-Succ Glc-Asn Glc-AsnNH4
3841 Wild type 266 ± 61 1,040 ± 230 231 ± 38 236 ± 41 1,317 ± 118 199 ± 7 202 ± 3 290 ± 5 229 ± 41
RU727 dctA::Ω 297 ± 25 1,362 ± 81 406 ± 57 2,011 ± 322 1,889 ± 233 1,777 ± 103 1,530 ± 214 782 ± 88 505 ± 71
RU730 dctB::Ω 184 ± 27 182 ± 43 266 ± 14 210 ± 8 75 ± 21 143 ± 27 65 ± 28 87 ± 63
RU711 dctD::Ω 150 ± 26 252 ± 62 191 ± 14 171 ± 25 211 ± 81 164 ± 37 85 ± 25 94 ± 5
RU865 ΔdctBD::Ω 168 ± 10 204 ± 44 117 ± 12 78 ± 21
RU714 ΔdctABD::Ω 179 ± 65 205 ± 35 123 ± 41 168 ± 51
RU929 ntrC::Ω 139 ± 10 93 ± 15
a

Results are shown as o-nitrophenylgalactoside hydrolyzed (in nanomoles per minute per milligram of protein ± SEM) and are based on at least three independent cultures assayed in triplicate. In all cases, the lacZ fusion is carried by pRU103. Unless otherwise stated, all compounds are at 10 mM concentrations. Glc, glucose; Me-Succ, 2-methyl succinate; DiMe-Succ, 2,2-dimethyl succinate.