Gopal-Srivastava R, Mallonee D H, White W B, Hylemon P B
Department of Microbiology and Immunology, Medical College of Virginia, Virginia Commonwealth University, Richmond 23298-0678.
J Bacteriol. 1990 Aug;172(8):4420-6. doi: 10.1128/jb.172.8.4420-4426.1990.
Eubacterium sp. strain VPI 12708 is an anaerobic intestinal bacterium which possesses inducible bile acid 7-dehydroxylation activity. Several new polypeptides are produced in this strain following induction with cholic acid. Genes coding for two copies of a bile acid-inducible 27,000-dalton polypeptide (baiA1 and baiA2) have been previously cloned and sequenced. We now report on a gene coding for a third copy of this 27,000-dalton polypeptide (baiA3). The baiA3 gene has been cloned in lambda DASH on an 11.2-kilobase DNA fragment from a partial Sau3A digest of the Eubacterium DNA. DNA sequence analysis of the baiA3 gene revealed 100% homology with the baiA1 gene within the coding region of the 27,000-dalton polypeptides. The baiA2 gene shares 81% sequence identity with the other two genes at the nucleotide level. The flanking nucleotide sequences associated with the baiA1 and baiA3 genes are identical for 930 bases in the 5' direction from the initiation codon and for at least 325 bases in the 3' direction from the stop codon, including the putative promoter regions for the genes. An additional open reading frame (occupying from 621 to 648 bases, depending on the correct start codon) was found in the identical 5' regions associated with the baiA1 and baiA3 clones. The 5' sequence 930 bases upstream from the baiA1 and baiA3 genes was totally divergent. The baiA2 gene, which is part of a large bile acid-inducible operon, showed no homology with the other two genes either in the 5' or 3' direction from the polypeptide coding region, except for a 15-base-pair presumed ribosome-binding site in the 5' region. These studies strongly suggest that a gene duplication (baiA1 and baiA3) has occurred and is stably maintained in this bacterium.
真杆菌属菌株VPI 12708是一种厌氧肠道细菌,具有可诱导的胆汁酸7-脱羟基活性。用胆酸诱导该菌株后会产生几种新的多肽。先前已克隆并测序了编码胆汁酸诱导的27,000道尔顿多肽的两个拷贝(baiA1和baiA2)的基因。我们现在报告编码该27,000道尔顿多肽第三个拷贝(baiA3)的基因。baiA3基因已克隆到λDASH载体上,该载体上的11.2千碱基DNA片段来自真杆菌DNA的部分Sau3A酶切片段。baiA3基因的DNA序列分析显示,在27,000道尔顿多肽的编码区域内,与baiA1基因有100%的同源性。baiA2基因在核苷酸水平上与其他两个基因有81%的序列同一性。与baiA1和baiA3基因相关的侧翼核苷酸序列,在起始密码子5'方向930个碱基以及终止密码子3'方向至少325个碱基上是相同的,包括这些基因的假定启动子区域。在与baiA1和baiA3克隆相关的相同5'区域中发现了一个额外的开放阅读框(根据正确的起始密码子,长度为621至648个碱基)。baiA1和baiA3基因上游930个碱基的5'序列完全不同。baiA2基因是一个大的胆汁酸诱导操纵子的一部分,除了在5'区域有一个15个碱基对的假定核糖体结合位点外,在多肽编码区域的5'或3'方向上与其他两个基因均无同源性。这些研究强烈表明,该细菌中发生了基因复制(baiA1和baiA3)并被稳定维持。