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通过表达设计的三乙酸内酯报告基因的重组大肠杆菌筛选增强的三乙酸内酯生产。

Screening for enhanced triacetic acid lactone production by recombinant Escherichia coli expressing a designed triacetic acid lactone reporter.

机构信息

Department of Chemical Engineering, Pennsylvania State University, 226A Fenske Laboratory, University Park, Pennsylvania 16802, USA.

出版信息

J Am Chem Soc. 2013 Jul 10;135(27):10099-103. doi: 10.1021/ja402654z. Epub 2013 Jul 1.

Abstract

Triacetic acid lactone (TAL) is a signature byproduct of polyketide synthases (PKSs) and a valuable synthetic precursor. We have developed an endogenous TAL reporter by engineering the Escherichia coli regulatory protein AraC to activate gene expression in response to TAL. The reporter enabled in vivo directed evolution of Gerbera hybrida 2-pyrone synthase activity in E. coli . Two rounds of mutagenesis and high-throughput screening yielded a variant conferring ~20-fold increased TAL production. The catalytic efficiency (kcat/Km) of the variant toward the substrate malonyl-CoA was improved 19-fold. This study broadens the utility of engineered AraC variants as customized molecular reporters. In addition, the TAL reporter can find applications in other basic PKS activity screens.

摘要

三乙酸内酯(TAL)是聚酮合酶(PKSs)的特征副产物,也是一种有价值的合成前体。我们通过工程化改造大肠杆菌调节蛋白 AraC 来开发内源性 TAL 报告基因,使其能够响应 TAL 激活基因表达。该报告基因使菊花 2-吡喃酮合酶活性在大肠杆菌中的体内定向进化成为可能。两轮诱变和高通量筛选得到了一个变体,使 TAL 的产量增加了约 20 倍。该变体对底物丙二酰辅酶 A 的催化效率(kcat/Km)提高了 19 倍。这项研究拓宽了工程化 AraC 变体作为定制分子报告基因的应用。此外,TAL 报告基因还可以应用于其他基本 PKS 活性筛选。

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