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用于羊毛硫抗生素Pep5工程改造的表达系统的构建

Construction of an expression system for engineering of the lantibiotic Pep5.

作者信息

Bierbaum G, Reis M, Szekat C, Sahl H G

机构信息

Institut für Medizinische Mikrobiologie und Immunologie der Universität Bonn, Germany.

出版信息

Appl Environ Microbiol. 1994 Dec;60(12):4332-8. doi: 10.1128/aem.60.12.4332-4338.1994.

DOI:10.1128/aem.60.12.4332-4338.1994
PMID:7811073
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC201989/
Abstract

Pep5 is a lanthionine-containing antimicrobial peptide which is produced by Staphylococcus epidermidis 5. Its structural gene, pepA, is located on the 20-kb plasmid pED503. A 6.2-kb fragment of pED503 containing pepA, the immunity gene pepI, and 5.4 kb of downstream sequence was able to direct biosynthesis of biologically active Pep5 in a nonproducing variant of the producer strain which is devoid of pED503. In addition to producing wild-type Pep5 with a molecular mass of 3,488 Da, the clone produced a peptide with an eightfold-lower bactericidal activity and a mass of 3,506 Da, indicative of incomplete dehydration of one hydroxyamino acid. For construction of the expression system, this 6.2-kb fragment was cut into a 1.39-kb fragment containing pepA and pepI and a 4.8-kb fragment covering the remaining downstream region. This 4.8-kb fragment was directly cloned into an Escherichia coli-Staphylococcus shuttle vector, yielding a new plasmid (pGB9) into which mutated pepA genes generated on the 1.39-kb fragment can be reinserted to yield a functional Pep5 biosynthesis gene cluster. To test the expression system, two mutants were constructed. Lys-18-Pro Pep5 was produced in its dehydrated form and a partially hydrated form in amounts comparable to those of the wild-type peptide. In contrast, only small amounts of Phe-23-Asp Pep5 were excreted, indicating that some residues in the propeptide part of the prelantibiotic may be crucial for certain steps in the biosynthetic pathway of lantibiotics.

摘要

Pep5是一种由表皮葡萄球菌5产生的含羊毛硫氨酸的抗菌肽。其结构基因pepA位于20 kb的质粒pED503上。pED503的一个6.2 kb片段,包含pepA、免疫基因pepI和5.4 kb的下游序列,能够在缺乏pED503的生产菌株的非生产变体中指导生物活性Pep5的生物合成。除了产生分子量为3488 Da的野生型Pep5外,该克隆还产生了一种杀菌活性低八倍、分子量为3506 Da的肽,这表明一种羟基氨基酸的脱水不完全。为构建表达系统,将这个6.2 kb的片段切割成一个1.39 kb的包含pepA和pepI的片段以及一个覆盖其余下游区域的4.8 kb片段。这个4.8 kb的片段直接克隆到一个大肠杆菌-葡萄球菌穿梭载体中,产生了一个新的质粒(pGB9),在1.39 kb片段上产生的突变pepA基因可以重新插入其中,以产生一个功能性的Pep5生物合成基因簇。为测试该表达系统,构建了两个突变体。Lys-18-Pro Pep5以脱水形式和部分水合形式产生,其产量与野生型肽相当。相比之下,仅分泌了少量的Phe-23-Asp Pep5,这表明前体羊毛硫抗生素前肽部分的一些残基可能对羊毛硫抗生素生物合成途径中的某些步骤至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2560/201989/8c9640ac4c5e/aem00029-0130-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2560/201989/8c9640ac4c5e/aem00029-0130-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2560/201989/8c9640ac4c5e/aem00029-0130-a.jpg

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