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来自古细菌沃氏甲烷球菌的色氨酸基因的克隆:trpBA基因的核苷酸序列

Cloning of the trp genes from the archaebacterium Methanococcus voltae: nucleotide sequence of the trpBA genes.

作者信息

Sibold L, Henriquet M

机构信息

Unité de Physiologie Cellulaire, Département des Biotechnologies, Institut Pasteur, Paris, France.

出版信息

Mol Gen Genet. 1988 Nov;214(3):439-50. doi: 10.1007/BF00330478.

Abstract

A cosmid bank of Methanococcus voltae DNA was obtained in Escherichia coli after ligation of partially HindIII-digested M. voltae DNA in the HindIII site of the transferable cosmid pVK100. The bank was used to perform complementation experiments with E. coli auxotrophic mutants. Five cosmids complementing trpA shared three adjacent HindIII fragments of 2.1, 2.3 and 14 kb. Two of these cosmids also complemented trpD and carried an additional 4.2 kb HindIII fragment. The trpA- and trpD- complementing regions were more precisely localized using Tn5 mutagenesis. A 1.7 kb PstI fragment, cloned into pUC9 in both orientations, was responsible for the trpA complementation. This fragment was sequenced and an open reading frame (ORF) of 852 nucleotides (ORFtrpA) encoding a 284 amino acid polypeptide of mol. wt. 31,938 was found. The amino acid sequence was compared with that of the alpha subunit of tryptophan synthase (trpA gene product) from nine eubacterial species and to the N-terminal part of the tryptophan synthase of Saccharomyces cerevisiae (TRP5 gene product). Similarity varied from 24% (Brevibacterium lactofermentum) to 35% (S. cerevisiae). The nucleotide sequence of the region upstream from M. voltae ORFtrpA was determined and revealed the presence of an ORF of 1227 nucleotides (ORFtrpB) encoding a 409 amino acid polypeptide of mol. wt. 44,634. The polypeptide sequence was similar to the beta subunit of tryptophan synthase (trpB gene product) from six eubacterial species and to the C-terminal part of the tryptophan synthase of S. cerevisiae. Similarity varied from 49% (S. cerevisiae, B. lactofermentum) to 58% (Pseudomonas aeruginosa). This high conservation supports the hypothesis of a common ancestor for the trpA and trpB genes of archaebacteria, eubacteria and eucaryotes. M. voltae ORFtrpA and ORFtrpB, which are transcribed in the same direction, are separated by a 37 bp AT-rich region. Immediately upstream from ORFtrpB, the 3' end of an ORF homologous to E. coli and Bacillus subtilis trpF was found. As the trpD-complementing region was located upstream from the trpFBA sequenced region, the organization of trp genes in the archaebacterium might thus be trpDFBA. Such an organization resembles that of enteric eubacteria, in which the trpEDCFBA genes are grouped in a single operon. However, M. voltae ORFtrpA and ORFtrpB do not overlap, in contrast with what is found in most eubacteria.

摘要

将部分经HindIII酶切的沃氏甲烷球菌(Methanococcus voltae)DNA连接到可转移黏粒pVK100的HindIII位点后,在大肠杆菌中构建了沃氏甲烷球菌DNA的黏粒文库。该文库用于对大肠杆菌营养缺陷型突变体进行互补实验。五个互补trpA的黏粒共享三个相邻的2.1、2.3和14 kb的HindIII片段。其中两个黏粒还互补trpD,并携带一个额外的4.2 kb HindIII片段。使用Tn5诱变更精确地定位了trpA和trpD互补区域。一个1.7 kb的PstI片段,以两种方向克隆到pUC9中,负责trpA互补。对该片段进行测序,发现了一个852个核苷酸的开放阅读框(ORFtrpA),编码一个分子量为31,938的284个氨基酸的多肽。将该氨基酸序列与来自9种真细菌的色氨酸合酶α亚基(trpA基因产物)以及酿酒酵母色氨酸合酶的N端部分(TRP5基因产物)进行了比较。相似性从24%(乳酸发酵短杆菌)到35%(酿酒酵母)不等。确定了沃氏甲烷球菌ORFtrpA上游区域的核苷酸序列,发现存在一个1227个核苷酸的ORF(ORFtrpB),编码一个分子量为44,634的409个氨基酸的多肽。该多肽序列与来自6种真细菌的色氨酸合酶β亚基(trpB基因产物)以及酿酒酵母色氨酸合酶的C端部分相似。相似性从49%(酿酒酵母、乳酸发酵短杆菌)到58%(铜绿假单胞菌)不等。这种高度保守支持了古细菌、真细菌和真核生物的trpA和trpB基因有共同祖先的假说。沃氏甲烷球菌的ORFtrpA和ORFtrpB转录方向相同,它们被一个37 bp的富含AT的区域隔开。在ORFtrpB紧邻上游,发现了一个与大肠杆菌和枯草芽孢杆菌trpF同源的ORF的3'端。由于trpD互补区域位于trpFBA测序区域的上游,因此古细菌中trp基因的组织可能是trpDFBA。这种组织类似于肠道真细菌,其中trpEDCFBA基因聚集在一个单一的操纵子中。然而,与大多数真细菌不同的是,沃氏甲烷球菌的ORFtrpA和ORFtrpB不重叠。

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