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通过将产生抗生素的聚酮合酶重新用于生产燃料和化学品而获得的对聚酮生物合成的见解。

Insights into polyketide biosynthesis gained from repurposing antibiotic-producing polyketide synthases to produce fuels and chemicals.

作者信息

Yuzawa Satoshi, Keasling Jay D, Katz Leonard

机构信息

QB3 Institute, University of California, Berkeley, CA 94720, USA.

Joint BioEnergy Institute, Emeryville, CA 94608, USA.

出版信息

J Antibiot (Tokyo). 2016 Jul;69(7):494-9. doi: 10.1038/ja.2016.64. Epub 2016 Jun 1.

Abstract

Complex polyketides comprise a large number of natural products that have broad application in medicine and agriculture. They are produced in bacteria and fungi from enzyme complexes named type I polyketide synthases (PKSs) that are composed of multifunctional polypeptides containing discrete enzymatic domains organized into modules. The modular nature of PKSs has enabled a multitude of efforts to engineer the PKS genes to produce novel polyketides with enhanced or new properties. We have repurposed PKSs, employing up to three modules to produce a number of short-chain molecules that could have applications as fuels or industrial chemicals. Examining the enzymatic functions in vitro of these repurposed PKSs, we have uncovered a number of expanded substrate specificities and requirements of various PKS domains not previously reported and determined an unexpected difference in the order of enzymatic reactions within a module. In addition, we were able to efficiently change the stereochemistry of side chains in selected PKS products.

摘要

复杂聚酮化合物包含大量在医学和农业中具有广泛应用的天然产物。它们由细菌和真菌中的一种名为I型聚酮合酶(PKS)的酶复合物产生,该复合物由多功能多肽组成,这些多肽包含组织成模块的离散酶结构域。PKS的模块化性质使得人们进行了大量努力来改造PKS基因,以产生具有增强或新特性的新型聚酮化合物。我们对PKS进行了重新利用,利用多达三个模块来生产一些可能用作燃料或工业化学品的短链分子。通过在体外研究这些重新利用的PKS的酶功能,我们发现了许多以前未报道的各种PKS结构域扩展的底物特异性和要求,并确定了模块内酶促反应顺序的意外差异。此外,我们能够有效地改变所选PKS产物中侧链的立体化学。

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