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聚酮化合物在异源宿主中的生物合成。

Biosynthesis of polyketides in heterologous hosts.

作者信息

Pfeifer B A, Khosla C

机构信息

Department of Chemical Engineering, Stanford University, Stanford, California 94305-5025, USA.

出版信息

Microbiol Mol Biol Rev. 2001 Mar;65(1):106-18. doi: 10.1128/MMBR.65.1.106-118.2001.

Abstract

Polyketide natural products show great promise as medicinal agents. Typically the products of microbial secondary biosynthesis, polyketides are synthesized by an evolutionarily related but architecturally diverse family of multifunctional enzymes called polyketide synthases. A principal limitation for fundamental biochemical studies of these modular megasynthases, as well as for their applications in biotechnology, is the challenge associated with manipulating the natural microorganism that produces a polyketide of interest. To ameliorate this limitation, over the past decade several genetically amenable microbes have been developed as heterologous hosts for polyketide biosynthesis. Here we review the state of the art as well as the difficulties associated with heterologous polyketide production. In particular, we focus on two model hosts, Streptomyces coelicolor and Escherichia coli. Future directions for this relatively new but growing technological opportunity are also discussed.

摘要

聚酮类天然产物作为药物具有巨大潜力。聚酮类化合物通常是微生物次生生物合成的产物,由一类进化相关但结构多样的多功能酶——聚酮合酶合成。这些模块化巨型合成酶的基础生化研究以及它们在生物技术中的应用面临的一个主要限制是,难以对产生目标聚酮化合物的天然微生物进行操作。为了改善这一限制,在过去十年中,人们开发了几种易于进行基因操作的微生物作为聚酮生物合成的异源宿主。在此,我们综述了该领域的现状以及异源生产聚酮化合物所面临的困难。特别地,我们重点关注两种模式宿主,即天蓝色链霉菌和大肠杆菌。我们还讨论了这一相对较新但不断发展的技术机会的未来发展方向。

相似文献

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Biosynthesis of polyketides in heterologous hosts.聚酮化合物在异源宿主中的生物合成。
Microbiol Mol Biol Rev. 2001 Mar;65(1):106-18. doi: 10.1128/MMBR.65.1.106-118.2001.
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Engineered polyketide biosynthesis and biocatalysis in Escherichia coli.大肠杆菌中的工程聚酮化合物生物合成和生物催化。
Appl Microbiol Biotechnol. 2010 Dec;88(6):1233-42. doi: 10.1007/s00253-010-2860-4. Epub 2010 Sep 19.

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