Turner M A, Eisenstark A
Mol Gen Genet. 1984;193(1):33-7. doi: 10.1007/BF00327410.
Escherichia coli cells in which the recA promoter is fused to a lac structural gene, (Mu) Mud(Ap,lac)::rec, were irradiated with two far-ultraviolet light wavelengths (254 and 290 nm), selected monochromatic near-ultraviolet (NUV) wavelengths 313 nm, 334 nm, 365 nm, or broad band solar-UV (290-420 nm) from a solar simulator. Irradiation with the two far-ultraviolet wavelengths was followed by high yields of beta-galactosidase, lambda prophage induction, and Weigle reactivation. These end points were not observed after irradiation with the selected NUV wavelengths or the broad spectrum solar-UV. Thus, neither broad spectrum solar-UV nor monochromatic NUV wavelengths resulted in the derepression of the recA promoter. Further, prior exposure of the cells either to the selected monochromatic NUV wavelengths or to solar-UV inhibited (a) the induction of beta-galactosidase by subsequent 254-nm radiation, (b) subsequent 254-nm induction of lambda prophage, (c) Weigle reactivation, and (d) mutation frequency. These observations are consistent with the hypothesis that NUV blocks subsequent recA protease action.
将recA启动子与lac结构基因融合的大肠杆菌细胞((Mu) Mud(Ap,lac)::rec),用两种远紫外光波长(254和290纳米)进行照射,从太阳模拟器中选择单色近紫外(NUV)波长313纳米、334纳米、365纳米,或宽带太阳紫外线(290 - 420纳米)。用这两种远紫外波长照射后,β - 半乳糖苷酶产量高、λ原噬菌体诱导和韦格勒再活化现象出现。在用选定的NUV波长或宽带太阳紫外线照射后,未观察到这些终点。因此,无论是宽带太阳紫外线还是单色NUV波长都不会导致recA启动子的去阻遏。此外,细胞事先暴露于选定的单色NUV波长或太阳紫外线,会抑制:(a) 随后254纳米辐射诱导的β - 半乳糖苷酶,(b) 随后254纳米诱导的λ原噬菌体,(c) 韦格勒再活化,以及(d) 突变频率。这些观察结果与NUV阻断随后recA蛋白酶作用的假设一致。