Regulatory sequences controlling short chain fatty acid metabolism in Escherichia coli.

C Y Chen, L A Hogarth, M S Shanley
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Abstract

Acetoacetate in Escherichia coli is metabolized via the combined enzymatic action of a CoA-transferase and a thiolase. Growth of E. coli on short chain fatty acids such as butyrate and valerate is also predicated upon the expression of these enzymes. The genes for these enzymes (atoDAB) are arranged in an operon and are coordinately transcribed in response to the inducer acetoacetate. A positive regulatory element, the product of the atoC gene, regulates expression of the operon. The atoC gene lies adjacent to the atoDAB operon and all the ato genes have been cloned as a single 6.2 kbp restriction fragment (kindly provided by Dr. Lauren Sallus Jenkins). We have isolated a series of mutant E. coli strains with altered regulatory properties that are either inducible by an alternate substrate, or that show constitutive expression of the atoDAB genes. The -10 and -35 regions upstream of the atoDAB operon poorly match consensus sequences. In addition, the transcriptional start is preceded by a catabolite activator protein binding site (CAP site), as well as a putative binding site for the atoC gene product as represented by a region of dyad symmetry.

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控制大肠杆菌短链脂肪酸代谢的调控序列。
乙酰乙酸在大肠杆菌中通过辅酶a转移酶和硫硫酶的联合酶作用进行代谢。大肠杆菌在短链脂肪酸如丁酸盐和戊酸盐上的生长也取决于这些酶的表达。这些酶(atdab)的基因排列在一个操纵子中,并响应于诱导剂乙酰乙酸酯进行协调转录。一个正调控元件,atoC基因的产物,调节操纵子的表达。atoC基因位于atdab操纵子附近,所有的ato基因都被克隆为一个6.2 kbp的限制性片段(由Dr. Lauren Sallus Jenkins提供)。我们已经分离出一系列具有改变的调节特性的突变大肠杆菌菌株,这些菌株要么被替代底物诱导,要么显示出atdab基因的组成表达。atdab操纵子上游的-10和-35区域与一致性序列不匹配。此外,在转录开始之前,有一个分解代谢激活蛋白结合位点(CAP位点),以及一个假定的atoC基因产物的结合位点,由一个二元对称区域表示。
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