Rossmann R, Sawers G, Böck A
Lehrstuhl für Mikrobiologie der Universität, München, Germany.
Mol Microbiol. 1991 Nov;5(11):2807-14. doi: 10.1111/j.1365-2958.1991.tb01989.x.
The products of a minimum of 15 genes are required for the synthesis of an active formate-hydrogenlyase (FHL) system in Escherichia coli. All are co-ordinately regulated in response to variations in the oxygen and nitrate concentration and the pH of the culture medium. Formate is obligately required for transcriptional activation of these genes. Analysis of the transcription of one of these genes, hycB linked to the lacZ reporter gene, revealed that oxygen and nitrate repression of transcription could be relieved completely, or partially in the case of nitrate, either by the addition of formate to the medium or by increasing the copy number of the gene encoding the transcriptional activator (fhlA) of this regulon. These studies uncovered a further level of regulation in which the transcription of hycB was reduced in cells grown on glucose. This effect was most clearly seen in aerobically grown cells when formate was added externally. Addition of cAMP overcame this glucose repression, which could be shown to be mediated by the cAMP receptor protein. These results would be consistent with the transport of formate being regulated by catabolite repression. Moreover, the repression of transcription through high pH also could be partially overcome by addition of increasing concentrations of formate to the medium, again being consistent with regulation at the level of formate import and export. Taken together, all these observations indicate that it is the intracellular level of formate that determines the transcription of the genes of the formate regulon by FhlA. This represents a novel positive feedback mechanism in which the activator of a regulon induces its own synthesis in response to increases in the concentration of the catabolic substrate, and this in turn is governed by the relative affinities of FhlA and the three formate dehydrogenase isoenzymes for formate.
在大肠杆菌中,合成一种活性甲酸 - 氢裂解酶(FHL)系统至少需要15个基因的产物。所有这些基因都会根据培养基中氧气、硝酸盐浓度以及pH值的变化进行协调调节。这些基因的转录激活绝对需要甲酸。对其中一个与lacZ报告基因相连的基因hycB的转录分析表明,通过向培养基中添加甲酸或增加编码该调控子转录激活因子(fhlA)的基因拷贝数,氧气和硝酸盐对转录的抑制作用可以完全解除,或者在硝酸盐的情况下部分解除。这些研究揭示了另一个调控层面,即在以葡萄糖为碳源生长的细胞中,hycB的转录会减少。当在需氧生长的细胞中外源添加甲酸时,这种效应最为明显。添加cAMP可克服这种葡萄糖抑制作用,且这种抑制作用可证明是由cAMP受体蛋白介导的。这些结果与甲酸的转运受分解代谢物阻遏调节一致。此外,通过向培养基中添加浓度不断增加的甲酸,也可以部分克服高pH对转录的抑制作用,这同样与甲酸进出口水平的调节一致。综上所述,所有这些观察结果表明,是细胞内甲酸水平通过FhlA决定了甲酸调控子基因的转录。这代表了一种新型的正反馈机制,即调控子的激活因子会响应分解代谢底物浓度的增加而诱导自身的合成,而这反过来又受FhlA和三种甲酸脱氢酶同工酶对甲酸的相对亲和力所控制。