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用于生产聚酮化合物类似物的基因工程。

Genetic engineering to produce polyketide analogues.

作者信息

Reeves Christopher D, Rodriguez Eduardo

机构信息

Amyris Biotechnologies, Inc., Emeryville, California, USA.

出版信息

Methods Enzymol. 2009;459:295-318. doi: 10.1016/S0076-6879(09)04613-8.

Abstract

Polyketides are pharmaceutically important and structurally diverse natural products. Creating analogues for drug development can be done with chemistry, but this is generally restricted to a few accessible functional groups. Analogues can also be made by genetic engineering, which is particularly effective for polyketides synthesized by a modular polyketide synthase (PKS). Such a PKS displays colinearity, which means that the structural features along the polyketide chain are determined by the catalytic specificities in corresponding modules along a molecular assembly line. The assembly line can be genetically engineered through addition, deletion, or mutation of catalytic domains or the reorganization of whole modules. Chemically synthesized precursors also can be fed to engineered assembly lines to further expand the repertoire of analogues. These various methods are discussed with an aim of providing a guide to the strategies most likely to succeed in a given circumstance. Recent information that could be relevant to future polyketide engineering projects is also discussed.

摘要

聚酮化合物是具有重要药学意义且结构多样的天然产物。通过化学方法可为药物开发创制类似物,但这通常局限于少数几个易于引入的官能团。类似物也可通过基因工程制备,这对于由模块化聚酮合酶(PKS)合成的聚酮化合物尤为有效。这样的PKS呈现共线性,即聚酮链上的结构特征由沿着分子装配线的相应模块中的催化特异性所决定。可通过催化结构域的添加、缺失或突变或整个模块的重组对装配线进行基因工程改造。化学合成的前体也可输入到工程化装配线中,以进一步拓展类似物的种类。本文对这些不同方法进行了讨论,旨在为在特定情况下最有可能成功的策略提供指导。还讨论了可能与未来聚酮化合物工程项目相关的最新信息。

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