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酵母同源重组克隆导致新型肽类 ambactin 和 xenolindicin。

Yeast homologous recombination cloning leading to the novel peptides ambactin and xenolindicin.

机构信息

Merck Stiftungsprofessur für Molekulare Biotechnologie, Fachbereich Biowissenschaften, Goethe Universität Frankfurt, Max-von-Laue Strasse 9, 60438 Frankfurt am Main (Germany).

出版信息

Chembiochem. 2014 Jun 16;15(9):1290-4. doi: 10.1002/cbic.201402065. Epub 2014 May 9.

Abstract

Heterologous production of GameXPeptide A (1), as well as of the novel peptide natural products ambactin (2) and xenolindicins A-C (3 a-c), was achieved by using the "overlap extension PCR-yeast homologous recombination" (ExRec) method. ExRec cloning is based on the ability of yeast to assemble overlapping DNA fragments into functional plasmids. Here we used this technique to clone a total of 15 biosynthesis gene clusters from Photorhabdus and Xenorhabdus with sizes of up to 45 kb. The structures of the novel compounds 2 and 3 a, which were produced in Escherichia coli, were elucidated by detailed MS and bioinformatics analysis, and additionally confirmed by their chemical synthesis.

摘要

通过使用“重叠延伸 PCR-酵母同源重组”(ExRec)方法,实现了 GameXPeptide A(1)以及新型肽天然产物 ambactin(2)和 xenolindicins A-C(3a-c)的异源生产。ExRec 克隆基于酵母将重叠 DNA 片段组装成功能质粒的能力。在这里,我们使用该技术从 Photorhabdus 和 Xenorhabdus 克隆了总共 15 个大小达 45kb 的生物合成基因簇。通过详细的 MS 和生物信息学分析阐明了在大肠杆菌中产生的新型化合物 2 和 3a 的结构,并通过其化学合成进一步证实。

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