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. 2001 Aug;183(15):4648–4651. doi: 10.1128/JB.183.15.4648-4651.2001

TABLE 1.

Expression of aprE′-′lacZ in B. subtilis strains carrying either multicopy degR or degU32(Hy) and degS200(Hy) mutations

Expt Straina Relevant genotype β-Galactosidase activityb Stimulationc
1 YY102(pNC6) relA+ 107 1
YY102(pNC61) relA+ multicopy degR 10,330 96
HT1013(pNC6) relA 18 1
HT1013(pNC61) relA multicopy degR 4,650 258
2 YY102 relA+ 133 1
YY202 relA+degU32(Hy) 9,380 70
YY299 relA+degS200(Hy) 7,260 54
HT1013 relA 20 1
HT1020 relA degU32(Hy) 1,020 51
HT1022 relA degS200(Hy) 820 41
a

Plasmids carried by the host strains are shown in parentheses. For strains YY102 and HT1013, refer to the legend to Fig. 1. Strains YY202 [trpC2 degU32(Hy) aprE::pSKK25] and YY299trpC2 [degS200(Hy) aprE::pSKK25] are the degU32(Hy) and degS200(Hy) derivatives, respectively, of YY102. Strains HT1020 [trpC2 degU32(Hy) relA::tet aprE::pSKK25] and HT1022 [trpC2 degS200(Hy) relA::tet aprE::pSKK25] are the degU32(Hy) and degS200(Hy) derivatives, respectively, of HT1013. 

b

β-Galactosidase activities in Miller units were measured at T0 through T5 as shown in Fig. 1, and the values shown are the peak values observed during this period. 

c

The values show the extent of stimulation caused by multicopy degR, degU32(Hy), and degS200(Hy) mutations relative to the control level, which was set as unity.