Spiro S, Guest J R
Department of Microbiology, University of Sheffield, UK.
J Gen Microbiol. 1987 Dec;133(12):3279-88. doi: 10.1099/00221287-133-12-3279.
The fnr gene of Escherichia coli encodes a transcriptional activator (FNR) which is required for the expression of a number of genes involved in anaerobic respiratory pathways. From the study of a translational fusion of fnr to the gene for beta-galactosidase (lacZ) it has been concluded that the fnr gene is expressed under both aerobic and anaerobic conditions and is subject to autoregulation and repression by glucose, particularly during anaerobic growth. These findings imply that during anaerobiosis the FNR protein adopts an active conformation, in which it functions both as a repressor of the fnr gene and as an activator of fnr-dependent genes. Sequences in the 5' non-coding region of fnr which could be involved in autoregulation are discussed. The fnr coding region was cloned into an expression vector which has allowed an amplification of FNR synthesis such that it accounts for about 2% of total cell protein. The ability to over-produce FNR in this way should be very useful for future biochemical studies.
大肠杆菌的fnr基因编码一种转录激活因子(FNR),许多参与厌氧呼吸途径的基因的表达都需要该因子。通过对fnr与β-半乳糖苷酶(lacZ)基因的翻译融合体的研究得出结论,fnr基因在有氧和无氧条件下均有表达,并且受到葡萄糖的自动调节和抑制,尤其是在厌氧生长期间。这些发现表明,在厌氧状态下,FNR蛋白呈现出一种活性构象,在这种构象中,它既作为fnr基因的阻遏物,又作为fnr依赖性基因的激活物发挥作用。文中讨论了fnr 5'非编码区中可能参与自动调节的序列。fnr编码区被克隆到一个表达载体中,该载体能够扩增FNR的合成,使其占细胞总蛋白的约2%。以这种方式过量产生FNR的能力对未来的生化研究应该非常有用。