Morbidoni H R, de Mendoza D, Cronan J E
Department of Microbiology, University of Illinois, Urbana 61801, USA.
J Bacteriol. 1996 Aug;178(16):4794-800. doi: 10.1128/jb.178.16.4794-4800.1996.
A cluster of Bacillus subtilis fatty acid synthetic genes was isolated by complementation of an Escherichia coli fabD mutant encoding a thermosensitive malonyl coenzyme A-acyl carrier protein transacylase. The B. subtilis genomic segment contains genes that encode three fatty acid synthetic proteins, malonyl coenzyme A-acyl carrier protein transacylase (fabD), 3-ketoacyl-acyl carrier protein reductase (fabG), and the N-terminal 14 amino acid residues of acyl carrier protein (acpP). Also present is a sequence that encodes a homolog of E. coli plsX, a gene that plays a poorly understood role in phospholipid synthesis. The B. subtilis plsX gene weakly complemented an E. coli plsX mutant. The order of genes in the cluster is plsX fabD fabG acpP, the same order found in E. coli, except that in E. coli the fabH gene lies between plsX and fabD. The absence of fabH in the B. subtilis cluster is consistent with the different fatty acid compositions of the two organisms. The amino acid sequence of B. subtilis acyl carrier protein was obtained by sequencing the purified protein, and the sequence obtained strongly resembled that of E. coli acyl carrier protein, except that most of the protein retained the initiating methionine residue. The B. subtilis fab cluster was mapped to the 135 to 145 degrees region of the chromosome.
通过对编码热敏丙二酰辅酶A-酰基载体蛋白转酰基酶的大肠杆菌fabD突变体进行互补,分离出了一簇枯草芽孢杆菌脂肪酸合成基因。枯草芽孢杆菌基因组片段包含编码三种脂肪酸合成蛋白的基因,即丙二酰辅酶A-酰基载体蛋白转酰基酶(fabD)、3-酮酰基-酰基载体蛋白还原酶(fabG)以及酰基载体蛋白(acpP)的N端14个氨基酸残基。还存在一个编码大肠杆菌plsX同源物的序列,该基因在磷脂合成中发挥的作用尚不清楚。枯草芽孢杆菌plsX基因对大肠杆菌plsX突变体有微弱的互补作用。该簇基因的顺序为plsX fabD fabG acpP,与大肠杆菌中的顺序相同,只是在大肠杆菌中fabH基因位于plsX和fabD之间。枯草芽孢杆菌簇中缺少fabH与这两种生物不同的脂肪酸组成是一致的。通过对纯化蛋白进行测序获得了枯草芽孢杆菌酰基载体蛋白的氨基酸序列,所得序列与大肠杆菌酰基载体蛋白的序列非常相似,只是该蛋白的大部分保留了起始甲硫氨酸残基。枯草芽孢杆菌fab簇被定位到染色体的135至145度区域。