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克拉维链霉菌中头孢菌素合成早期步骤基因表达的相互依赖性

Interdependence of gene expression for early steps of cephalosporin synthesis in Streptomyces clavuligerus.

作者信息

Demain A L, Piret J M, Yu H, Coque J J, Liras P, Martin J F

机构信息

Department of Biology, Massachusettes Institute of Technology, Cambridge 02139.

出版信息

Ann N Y Acad Sci. 1994 May 2;721:117-22. doi: 10.1111/j.1749-6632.1994.tb47383.x.

Abstract

The early steps of cephamycin synthesis by S. clavuligerus are catalyzed sequentially by lysine epsilon-aminotransferase (LAT), delta-(L-alpha-aminoadipyl)-L-cysteinyl-D-valine synthetase (ACVS) and isopenicillin N synthase (cyclase, IPNS). The genes (lat, pcbAB, and pcbC, respectively) are closely linked in the same order as the enzymes act in the biosynthetic pathway and are transcribed in the same direction. Four cephamycin non- (or low-) producing mutants are pleiotropic in that they have undetectable or markedly diminished levels of ACVS and cyclase; two mutants almost completely lack LAT activity. All four mutants are complemented in cephamycin formation by transformation with pNBR1, a plasmid containing a 7.2-kb genomic region of S. clavuligerus in vector pIJ702. The cloned DNA was found to possess no part of the cyclase gene, but instead it contained lat and the 5' upstream part of pcbAB. Doran et al. reported that the 31-bp region between pcbAB and pcbC contains no recognizable promoter or transcription termination sequences. We found that there are 153 bp between the lat ORF and the pcbAB start codon. A potential transcriptional terminator begins 4 to 6 bp downstream of the lat ORF. In the 111-bp segment between the end of the "terminator" and the pcbAB start codon, there are no Streptomyces-like or Escherichia coli-like promoter consensus sequences. However, upstream of the "terminator," that is, in the downstream portion of the lat ORF, are two regions resembling a Streptomyces consensus promoter. Promoter activity in gene fusion constructions was demonstrated in this region. A third potential promoter is upstream of the lat ORF, but only the--10 part is on the cloned DNA. The mechanism by which the cloned DNA (containing lat, the 5' part of pcbAB, and the intervening sequence) influences the expression of the downstream genes encoding ACVS and IPNS, even in strains that possess LAT activity, is an intriguing target of future investigation.

摘要

棒状链霉菌合成头霉素的早期步骤依次由赖氨酸ε-氨基转移酶(LAT)、δ-(L-α-氨基己二酰基)-L-半胱氨酰-D-缬氨酸合成酶(ACVS)和异青霉素N合酶(环化酶,IPNS)催化。这些基因(分别为lat、pcbAB和pcbC)紧密连锁,其顺序与酶在生物合成途径中的作用顺序相同,且转录方向一致。四个不产生(或低产)头霉素的突变体具有多效性,即它们的ACVS和环化酶水平检测不到或显著降低;两个突变体几乎完全缺乏LAT活性。通过用pNBR1转化,所有四个突变体在头霉素形成方面都得到了互补,pNBR1是一种质粒,在载体pIJ702中含有棒状链霉菌的一个7.2 kb基因组区域。发现克隆的DNA不包含环化酶基因的任何部分,但它包含lat和pcbAB的5'上游部分。多兰等人报道,pcbAB和pcbC之间的31 bp区域不包含可识别的启动子或转录终止序列。我们发现lat开放阅读框(ORF)与pcbAB起始密码子之间有153 bp。一个潜在的转录终止子在lat ORF下游4至6 bp处开始。在“终止子”末端与pcbAB起始密码子之间的111 bp片段中,没有链霉菌样或大肠杆菌样启动子共有序列。然而,在“终止子”上游,即在lat ORF的下游部分,有两个类似于链霉菌共有启动子的区域。在该区域的基因融合构建体中证明了启动子活性。第三个潜在启动子在lat ORF上游,但只有-10部分在克隆的DNA上。即使在具有LAT活性的菌株中,克隆的DNA(包含lat、pcbAB的5'部分和中间序列)影响编码ACVS和IPNS的下游基因表达的机制,是未来研究的一个有趣目标。

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