Wanner B L, Kodaira R, Neidhardt F C
J Bacteriol. 1978 Dec;136(3):947-54. doi: 10.1128/jb.136.3.947-954.1978.
The physiological state of Escherichia coli with respect to (permanent) catabolite repression was assessed by measuring the steady-state level of beta-galactosidase in induced or in constitutive cells under a variety of growth conditions. Four results were obtained. (i) Catabolite repression had a major effect on fully induced or constitutive expression of the lac gene, and the magnitude of this effect was found to be dependent on the promoter structure; cells with a wild-type lac promoter showed an 18-fold variation in lac expression, and cells with the lacP37 (formerly lac-L37) promoter exhibited several hundred-fold variation. (ii) Exogenous adenosine cyclic 3',5'-monophosphoric acid (cAMP) could not abolish catabolite repression, even though several controls demonstrated that cAMP was entering the cells in significant amounts. (Rapid intracellular degradation of cAMP could not be ruled out.) (iii) Neither the growth rate nor the presence of biosynthetic products altered the degree of catabolite repression; all variation could be related to the catabolites present in the growth medium. (iv) Slowing by imposing an amino acid restriction decreased the differential rate of beta-galactosidase synthesis from the wild-type lac promoter when bacteria were cultured in either the absence or presence of cAMP; this decreased lac expression also occurred when the bacteria harbored the catabolite-insensitive lacP5 (formerly lacUV5) promoter mutation. These findings support the idea that (permanent) catabolite repression is set by the catabolites in the growth medium and may not be related to an imbalance between catabolism and anabolism.
通过在多种生长条件下测量诱导型或组成型细胞中β-半乳糖苷酶的稳态水平,评估了大肠杆菌相对于(永久性)分解代谢物阻遏的生理状态。得到了四个结果。(i)分解代谢物阻遏对lac基因的完全诱导表达或组成型表达有主要影响,并且发现这种影响的程度取决于启动子结构;具有野生型lac启动子的细胞在lac表达上显示出18倍的差异,而具有lacP37(以前的lac-L37)启动子的细胞表现出数百倍的差异。(ii)外源性腺苷3',5'-环磷酸(cAMP)不能消除分解代谢物阻遏,尽管多项对照表明cAMP大量进入细胞。(不能排除cAMP在细胞内快速降解的可能性。)(iii)生长速率和生物合成产物的存在均未改变分解代谢物阻遏的程度;所有差异都可能与生长培养基中存在的分解代谢物有关。(iv)当细菌在有无cAMP的情况下培养时,通过施加氨基酸限制来减缓生长,会降低来自野生型lac启动子的β-半乳糖苷酶合成的差异速率;当细菌携带对分解代谢物不敏感的lacP5(以前的lacUV5)启动子突变时,也会出现这种lac表达降低的情况。这些发现支持这样一种观点,即(永久性)分解代谢物阻遏是由生长培养基中的分解代谢物设定的,可能与分解代谢和合成代谢之间的失衡无关。