Wells J E, Hylemon P B
Department of Microbiology and Immunology, Medical College of Virginia Campus, Virginia Commonwealth University, Richmond, Virginia 23298, USA.
Appl Environ Microbiol. 2000 Mar;66(3):1107-13. doi: 10.1128/AEM.66.3.1107-1113.2000.
Clostridium sp. strain TO-931 can rapidly convert the primary bile acid cholic acid to a potentially toxic compound, deoxycholic acid. Mixed oligonucleotide probes were used to isolate a gene fragment encoding a putative bile acid transporter from Clostridium sp. strain TO-931. This DNA fragment had 60% nucleotide sequence identity to a known bile acid transporter gene from Eubacterium sp. strain VPI 12708, another bile acid-7alpha-dehydroxylating intestinal bacterium. The DNA (9.15 kb) surrounding the transporter gene was cloned from Clostridium sp. strain TO-931 and sequenced. Within this larger DNA fragment was a 7.9-kb region, containing six successive open reading frames (ORFs), that was encoded by a single 8.1-kb transcript, as determined by Northern blot analysis. The gene arrangement and DNA sequence of the Clostridium sp. strain TO-931 operon are similar to those of a Eubacterium sp. strain VPI 12708 bile acid-inducible operon containing nine ORFs. Several genes in the Eubacterium sp. strain VPI 12708 operon have been shown to encode products required for bile acid 7alpha-dehydroxylation. In Clostridium sp. strain TO-931, genes potentially encoding bile acid-coenzyme A (CoA) ligase, 3alpha-hydroxysteroid dehydrogenase, bile acid 7alpha-dehydratase, bile acid-CoA hydrolase, and a bile acid transporter were similar in size and exhibited amino acid homology to similar gene products from Eubacterium sp. strain VPI 12708 (encoded by baiB, baiA, baiE, baiF, and baiG, respectively). However, no genes similar to Eubacterium sp. strain VPI 12708 biaH or baiI were found in the Clostridium sp. strain TO-931 bai operon, and the two putative Eubacterium sp. strain VPI 12708 genes, baiC and baiD, were arranged in one continuous ORF in Clostridium sp. strain TO-931. Intergene regions showed no significant DNA sequence similarity, but primer extension analysis identified a region 115 bp upstream from the first ORF that exhibited 58% identity to a bai operator/promoter region identified in Eubacterium sp. strain VPI 12708. These results indicate that the gene organization, gene product amino acid sequences, and promoters of the bile acid-inducible operons of Clostridium sp. strain TO-931 and Eubacterium sp. strain VPI 12708 are highly conserved.
梭菌属菌株TO - 931可迅速将初级胆汁酸胆酸转化为一种潜在的有毒化合物——脱氧胆酸。混合寡核苷酸探针被用于从梭菌属菌株TO - 931中分离出一个编码假定胆汁酸转运蛋白的基因片段。该DNA片段与来自另一种胆汁酸7α - 脱羟基肠道细菌——真杆菌属菌株VPI 12708的已知胆汁酸转运蛋白基因具有60%的核苷酸序列同一性。围绕该转运蛋白基因的DNA(9.15 kb)从梭菌属菌株TO - 931中克隆出来并进行了测序。通过Northern印迹分析确定,在这个更大的DNA片段内有一个7.9 kb的区域,包含六个连续的开放阅读框(ORF),由一个单一的8.1 kb转录本编码。梭菌属菌株TO - 931操纵子的基因排列和DNA序列与含有九个ORF的真杆菌属菌株VPI 12708胆汁酸诱导型操纵子相似。真杆菌属菌株VPI 12708操纵子中的几个基因已被证明编码胆汁酸7α - 脱羟基所需的产物。在梭菌属菌株TO - 931中,潜在编码胆汁酸 - 辅酶A(CoA)连接酶、3α - 羟基类固醇脱氢酶、胆汁酸7α - 脱水酶、胆汁酸 - CoA水解酶和一种胆汁酸转运蛋白的基因在大小上相似,并且与来自真杆菌属菌株VPI 12708的类似基因产物(分别由baiB、baiA、baiE、baiF和baiG编码)表现出氨基酸同源性。然而,在梭菌属菌株TO - 931的bai操纵子中未发现与真杆菌属菌株VPI 12708的biaH或baiI相似的基因,并且真杆菌属菌株VPI 12708的两个假定基因baiC和baiD在梭菌属菌株TO - 931中排列在一个连续的ORF中。基因间区域未显示出明显的DNA序列相似性,但引物延伸分析确定了第一个ORF上游115 bp处的一个区域,该区域与在真杆菌属菌株VPI 12708中鉴定出的bai操纵子/启动子区域具有58%的同一性。这些结果表明,梭菌属菌株TO - 931和真杆菌属菌株VPI 12708的胆汁酸诱导型操纵子的基因组织、基因产物氨基酸序列和启动子高度保守。