Birkmann A, Zinoni F, Sawers G, Böck A
Arch Microbiol. 1987 Jun;148(1):44-51. doi: 10.1007/BF00429646.
The regulatory elements involved in expression of the gene (fdhF) for the selenopolypeptide of formate dehydrogenase and of a gene (or transcriptional unit) (hyd) specifically responsible for the formation of the gas-evolving hydrogenase (hydrogenase 3) in Escherichia coli were investigated. Formate (or a product of it) is required for expression of both systems since in a pyruvate-formate-lyase deficient mutant induction occurs only when formate is supplemented externally. Under this condition, formate can partially overcome repression by nitrate. The transcription of both the fdhF gene and the hydrogenase-3-encoding systems is independent of the presence of a wild-type fnr gene when formate is present, supporting the view that the Fnr effect on the formation of the formate-hydrogen-lyase pathway is indirect. Mutations blocking the synthesis of a functional molybdenum cofactor also had no major affect on fdhF and hyd expression. The nucleotide sequence of the 5' flanking region of the fdhF gene was determined and the transcription start point of the fdhF gene was localized by nuclease S1 mapping. Nuclease Bal31 generated deletion clones were constructed and the regulation of their expression was studied. Anaerobic expression and induction by formate depended on the presence of a stretch of approximately 185 nucleotides upstream of the translation start. Elements mediating formate induction and oxygen or nitrate repression could not be separated physically. The regulatory features of the fdhF upstream region bear striking resemblance to systems whose expression are dependent upon upstream activating elements.
对大肠杆菌中甲酸脱氢酶的硒代多肽基因(fdhF)以及专门负责产气氢化酶(氢化酶3)形成的基因(或转录单元)(hyd)表达所涉及的调控元件进行了研究。这两个系统的表达都需要甲酸(或其产物),因为在丙酮酸甲酸裂解酶缺陷型突变体中,只有在外部添加甲酸时才会发生诱导。在这种情况下,甲酸可以部分克服硝酸盐的抑制作用。当存在甲酸时,fdhF基因和氢化酶3编码系统的转录都不依赖于野生型fnr基因的存在,这支持了Fnr对甲酸 - 氢裂解酶途径形成的影响是间接的这一观点。阻断功能性钼辅因子合成的突变对fdhF和hyd的表达也没有重大影响。测定了fdhF基因5'侧翼区域的核苷酸序列,并通过核酸酶S1图谱定位了fdhF基因的转录起始点。构建了核酸酶Bal31产生的缺失克隆,并研究了它们的表达调控。厌氧表达和甲酸诱导取决于翻译起始上游一段约185个核苷酸的存在。介导甲酸诱导以及氧气或硝酸盐抑制的元件在物理上无法分离。fdhF上游区域的调控特征与那些表达依赖于上游激活元件的系统有显著相似之处。