Roberts J W, Roberts C W, Craig N L
Proc Natl Acad Sci U S A. 1978 Oct;75(10):4714-8. doi: 10.1073/pnas.75.10.4714.
Phage lambda repressor is inactivated and cleaved into two detectable fragments during incubation with purified Escherichia coli recA gene protein in vitro, in a reaction that requires ATP. This reaction reproduces the recA-dependent inactivation of repressor that occurs in vivo during induction of the SOS functions. The proteolytic activity may reside in the recA protein itself and may be a fundamental activity of it.
在体外与纯化的大肠杆菌recA基因蛋白一起温育期间,噬菌体λ阻遏物会失活并被切割成两个可检测的片段,该反应需要ATP。此反应重现了在SOS功能诱导期间体内发生的阻遏物的recA依赖性失活。蛋白水解活性可能存在于recA蛋白本身中,并且可能是其基本活性。