Li S J, Cronan J E
Department of Microbiology, University of Illinois, Urbana-Champaign 61801.
J Bacteriol. 1993 Jan;175(2):332-40. doi: 10.1128/jb.175.2.332-340.1993.
Acetyl coenzyme A (CoA) carboxylase catalyzes the synthesis of malonyl-CoA, the first intermediate of fatty acid synthesis. The Escherichia coli enzyme is encoded by four subunits located at three different positions on the E. coli chromosome. The accBC genes lie in a small operon at min 72, whereas accA and accD are located at min 4.3 and 50, respectively. We examined the expression of the genes that encode the E. coli acetyl-CoA carboxylase subunits (accA, accBC, and accD) under a variety of growth conditions by quantitative Northern (RNA) blot analysis. We found a direct correlation between the levels of transcription of the acc genes and the rate of cellular growth. Consistent results were also obtained upon nutritional upshift and downshift experiments and upon dilution of stationary-phase cultures into fresh media. We also determined the 5' end of the accA and accD mRNAs by primer extension and did transcriptional fusion analysis of the previously reported accBC promoter. Several interesting features were found in the promoter regions of these genes, including a bent DNA sequence and an open reading frame within the unusually long leader mRNA of the accBC operon, potential stem-loop structures in the accA and accD mRNA leader regions, and a stretch of GC-rich sequences followed by AT-rich sequences common to all three promoters. In addition, both accA and accD are located in complex gene clusters. For example, the accA promoter was localized within the upstream polC gene (which encodes the DNA polymerase III catalytic subunit), suggesting that additional regulatory mechanisms exist.
乙酰辅酶A(CoA)羧化酶催化丙二酸单酰辅酶A的合成,丙二酸单酰辅酶A是脂肪酸合成的第一个中间产物。大肠杆菌的这种酶由位于大肠杆菌染色体上三个不同位置的四个亚基编码。accBC基因位于72分钟处的一个小操纵子中,而accA和accD分别位于4.3分钟和50分钟处。我们通过定量Northern(RNA)印迹分析,检测了在多种生长条件下编码大肠杆菌乙酰辅酶A羧化酶亚基(accA、accBC和accD)的基因的表达情况。我们发现acc基因的转录水平与细胞生长速率之间存在直接相关性。在营养上调和下调实验以及将稳定期培养物稀释到新鲜培养基中时,也得到了一致的结果。我们还通过引物延伸确定了accA和accD mRNA的5'端,并对先前报道的accBC启动子进行了转录融合分析。在这些基因的启动子区域发现了几个有趣的特征,包括accBC操纵子异常长的前导mRNA中的弯曲DNA序列和一个开放阅读框、accA和accD mRNA前导区域中的潜在茎环结构以及所有三个启动子共有的一段富含GC序列后接富含AT序列。此外,accA和accD都位于复杂的基因簇中。例如,accA启动子位于上游的polC基因(编码DNA聚合酶III催化亚基)内,这表明存在其他调控机制。