Manchester Institute of Biotechnology, Department of Chemical Engineering, The University of Manchester, 131 Princess Street, Manchester M1 7DN, UK.
Int J Mol Sci. 2024 Aug 6;25(16):8567. doi: 10.3390/ijms25168567.
During gliotoxin biosynthesis in fungi, the cytochrome P450 GliF enzyme catalyzes an unusual C-N ring-closure step while also an aromatic ring is hydroxylated in the same reaction cycle, which may have relevance to drug synthesis reactions in biotechnology. However, as the details of the reaction mechanism are still controversial, no applications have been developed yet. To resolve the mechanism of gliotoxin biosynthesis and gain insight into the steps leading to ring-closure, we ran a combination of molecular dynamics and density functional theory calculations on the structure and reactivity of P450 GliF and tested a range of possible reaction mechanisms, pathways and models. The calculations show that, rather than hydrogen atom transfer from the substrate to Compound I, an initial proton transfer transition state is followed by a fast electron transfer en route to the radical intermediate, and hence a non-synchronous hydrogen atom abstraction takes place. The radical intermediate then reacts by OH rebound to the aromatic ring to form a biradical in the substrate that, through ring-closure between the radical centers, gives gliotoxin products. Interestingly, the structure and energetics of the reaction mechanisms appear little affected by the addition of polar groups to the model and hence we predict that the reaction can be catalyzed by other P450 isozymes that also bind the same substrate. Alternative pathways, such as a pathway starting with an electrophilic attack on the arene to form an epoxide, are high in energy and are ruled out.
在真菌的Gliotoxin 生物合成过程中,细胞色素 P450 GliF 酶催化一个不寻常的 C-N 环闭合步骤,同时在同一反应循环中芳香环被羟化,这可能与生物技术中的药物合成反应有关。然而,由于反应机制的细节仍存在争议,因此尚未开发出应用。为了解决Gliotoxin 生物合成的机制,并深入了解导致环闭合的步骤,我们对 P450 GliF 的结构和反应性进行了分子动力学和密度泛函理论计算的组合,并测试了一系列可能的反应机制、途径和模型。计算表明,不是从底物向化合物 I 转移氢原子,而是接着初始质子转移过渡态发生快速电子转移,从而发生非同步的氢原子提取。然后,自由基中间体通过 OH 反弹到芳环上,在底物中形成双自由基,通过自由基中心之间的环闭合,生成Gliotoxin 产物。有趣的是,反应机制的结构和能量似乎受模型中添加极性基团的影响很小,因此我们预测其他也结合相同底物的 P450 同工酶也可以催化该反应。例如,通过芳环的亲电攻击形成环氧化物的途径,能量较高,因此被排除。