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A Turnstile Mechanism for the Controlled Growth ofBiosynthetic Intermediates on Assembly Line Polyketide Synthases

机译:受控生长的转闸机制。组装线聚酮化合物合酶上的生物合成中间体

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摘要

Vectorial polyketide biosynthesis on an assembly line polyketide synthase is the most distinctive property of this family of biological machines, while providing the key conceptual tool for the bioinformatic decoding of new antibiotic pathways. We now show that the action of the entire assembly line is synchronized by a previously unrecognized turnstile mechanism that prevents the ketosynthase domain of each module from being acylated by a new polyketide chain until the product of the prior catalytic cycle has been passed to the downstream module from the corresponding acyl carrier protein domain. The turnstile is closed by virtue of tight coupling to the signature decarboxylative condensation reaction catalyzed by the ketosynthase domain of each polyketide synthase module. Reopening of the turnstile is coupled to the eventual chain translocation step that vacates the module. At the maximal rate of substrate turnover, one would expect the chain release step to initiate a cascade of chain translocation events that sequentially migrate back upstream, thereby repriming each moduleand setting up the assembly line for the next round of polyketidechain elongation.
机译:流水线型聚酮化合物合酶上的矢量聚酮化合物生物合成是该系列生物机器最独特的特性,同时为新抗生素途径的生物信息学解码提供了关键的概念工具。现在我们表明,整个装配线的动作是由先前无法识别的旋转机制同步的,该机制防止每个模块的酮合酶结构域被新的聚酮化合物链酰化,直到先前催化循环的产物传递到下游模块为止来自相应的酰基载体蛋白结构域。旋转门通过与每个聚酮化合物合酶模块的酮合酶结构域催化的特征性脱羧缩合反应紧密偶联而封闭。旋转栅门的重新打开与最终腾空模块的链转移步骤相关。以最大的底物周转率,人们会期望链释放步骤会引发一连串的链转移事件,随后顺次迁移回上游,从而重新启动每个模块并建立下一轮聚酮化合物的生产线链伸长。

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