Heincz M C, McFall E
J Bacteriol. 1978 Oct;136(1):104-10. doi: 10.1128/jb.136.1.104-110.1978.
Cyclic AMP is required for optimal synthesis of D-serine deaminase synthesis from dsdO+ templates and for optimal hyperinducible synthesis from low constitutive dsdO templates both in vitro and in vivo. Neither D-serine, cyclic AMP, nor dsdC activator has an effect on expression of a high constitutive dsdO template. The synthesis of the dsdC activator itself in vitro is independent of cyclic AMP. Guanosine tetraphosphate does not have a significant effect on in vitro D-serine deaminase synthesis from dsdO+ or dsdO templates. A previously described class of dsdO mutants showing partial catabolite sensitivity of constitutive D-serine deaminase synthesis proved to be low dsdO types. They all contain a low constitutive dsdC mutation; the two effects are additive with regard to level of constitutivity, but only that portion of synthesis attributable to the dsdC mutation is cyclic AMP dependent.
环磷酸腺苷(cAMP)对于从dsdO⁺模板最佳合成D-丝氨酸脱氨酶以及从低组成型dsdO模板在体外和体内实现最佳超诱导合成都是必需的。D-丝氨酸、环磷酸腺苷或dsdC激活剂对高组成型dsdO模板的表达均无影响。dsdC激活剂本身在体外的合成不依赖于环磷酸腺苷。四磷酸鸟苷对从dsdO⁺或dsdO模板体外合成D-丝氨酸脱氨酶没有显著影响。先前描述的一类dsdO突变体,其组成型D-丝氨酸脱氨酶合成表现出部分分解代谢物敏感性,结果证明是低dsdO类型。它们都含有一个低组成型dsdC突变;就组成型水平而言,这两种效应是相加的,但只有可归因于dsdC突变的那部分合成是依赖环磷酸腺苷的。