Department of Chemistry, University of Notre Dame, Notre Dame, USA.
Nat Prod Rep. 2013 Oct 11;30(11):1391-411. doi: 10.1039/c3np70060g.
Heterologous expression of biosynthetic pathways is an indispensable tool in the discovery, production, engineering, and characterization of bacterial polyketides and the complex enzymology involved in their biosynthesis. Ensuring transcription of polyketide biosynthetic gene clusters in heterologous hosts is a pressing problem. This review evaluates the two strategies used to ensure transcription. The first is a promoter replacement approach where promoters known to function in the heterologous host are inserted into the biosynthetic gene cluster. The second is an approach that relies on the heterologous host recognizing and utilizing promoters native to the gene cluster. Both have been successful methodologies and have different strengths and weaknesses, which are highlighted and discussed.
异源表达生物合成途径是发现、生产、工程和表征细菌聚酮化合物以及涉及它们生物合成的复杂酶学的不可或缺的工具。确保在异源宿主中转录聚酮生物合成基因簇是一个紧迫的问题。本综述评估了用于确保转录的两种策略。第一种方法是启动子替换方法,即将在异源宿主中已知起作用的启动子插入生物合成基因簇中。第二种方法是依赖于异源宿主识别和利用基因簇中原有的启动子的方法。这两种方法都是成功的方法,具有不同的优缺点,本文对此进行了强调和讨论。