Department of Organic Chemistry, Arrhenius Laboratory, Stockholm University, SE-10691, Stockholm, Sweden.
Angew Chem Int Ed Engl. 2020 Dec 14;59(51):22973-22977. doi: 10.1002/anie.202008919. Epub 2020 Oct 16.
The enzyme 3-methylglutaconyl coenzyme A (CoA) decarboxylase (called AibA/AibB) catalyzes the decarboxylation of 3-methylglutaconyl CoA to generate 3,3-dimethylacrylyl-CoA, representing an important step in the biosynthesis of isovaleryl-coenzyme A in Myxococcus xanthus when the regular pathway is blocked. A novel mechanism involving a pericyclic transition state has previously been proposed for this enzyme, making AibA/AibB unique among decarboxylases. Herein, density functional calculations are used to examine the energetic feasibility of this mechanism. It is shown that the intramolecular pericyclic reaction is associated with a very high energy barrier that is similar to the barrier of the same reaction in the absence of the enzyme. Instead, the calculations show that a direct decarboxylation mechanism has feasible energy barriers that are in line with the experimental observations.
酶 3-甲基戊二酰辅酶 A(CoA)脱羧酶(称为 AibA/AibB)催化 3-甲基戊二酰 CoA 的脱羧生成 3,3-二甲基丙烯酰-CoA,当正常途径受阻时,这代表了黄色粘球菌异戊酰辅酶 A 生物合成中的一个重要步骤。先前已经提出了一种涉及周环过渡态的新机制,使 AibA/AibB 在脱羧酶中独一无二。在此,密度泛函计算被用于研究该机制的能量可行性。结果表明,分子内周环反应伴随着非常高的能垒,该能垒与没有酶时相同反应的能垒相似。相反,计算表明直接脱羧机制具有可行的能垒,与实验观察结果一致。