Cox Russell J
Institute for Organic Chemistry and BMWZ, Leibniz University of Hannover, Schneiderberg 38, 30167, Hannover, Germany.
Nat Prod Rep. 2023 Jan 25;40(1):9-27. doi: 10.1039/d2np00007e.
Covering: 1996-2022Investigations over the last 2 decades have begun to reveal how fungal iterative highly-reducing polyketide synthases are programmed. Both and experiments have revealed the interplay of intrinsic and extrinsic selectivity of the component catalytic domains of these systems. Structural biology has begun to provide high resolution structures of hr-PKS that can be used as the basis for their engineering and reprogramming, but progress to-date remains rudimentary. However, significant opportunities exist for translating the current level of understanding into the ability to rationally re-engineer these highly efficient systems for the production of important biologically active compounds through biotechnology.
1996年至2022年
过去20年的研究已开始揭示真菌迭代高度还原聚酮合酶是如何被编程的。 和 实验都揭示了这些系统中各组成催化结构域的内在和外在选择性之间的相互作用。结构生物学已开始提供hr-PKS的高分辨率结构,可作为其工程改造和重新编程的基础,但迄今为止进展仍很初步。然而,将目前的理解水平转化为通过生物技术合理地重新设计这些高效系统以生产重要生物活性化合物的能力,存在着重大机遇。