Yoshimura Masataka, Arai Munehito
Department of Life Sciences, Graduate School of Arts and Sciences, The University of Tokyo, Tokyo 153-8902, Japan.
Department of Physics, Graduate School of Science, The University of Tokyo, Tokyo 153-8902, Japan.
Biophys Physicobiol. 2025 Jan 9;22(1):e220003. doi: 10.2142/biophysico.bppb-v22.0003. eCollection 2025.
Cyanobacteria can produce alkanes equivalent to diesel fuels through a two-step enzymatic process involving acyl-(acyl carrier protein) reductase (AAR) and aldehyde deformylating oxygenase (ADO), providing a potential renewable biofuel source. AAR binds to ADO for efficient delivery of an aldehyde substrate and they have been proposed to dissociate when the alkane product is released from the same site as the substrate entrance of ADO. However, the dynamics of the substrate and product in ADO during substrate entry and product release are poorly understood. Here, we performed molecular dynamics (MD) simulations of ADO in the presence of substrate or product. We found that while the aldehyde substrate remains close to the active center of ADO before catalysis, the alkane product can dynamically rotate within the hydrophobic tunnel inside ADO toward the product exit after catalysis. Furthermore, the parallel cascade selection (PaCS)-MD simulations of ADO and the AAR/ADO complex identified the locations of the substrate entrance and the multiple exits for product release on ADO. Strikingly, the PaCS-MD simulations revealed that the alkane product can be released from the exit different from the substrate entrance without dissociation of AAR. Based on these results, we propose a reaction model for efficient alkane production by the AAR/ADO complex in which aldehydes and alkanes are synthesized simultaneously while AAR and ADO remain bound, and the aldehyde substrate can be delivered to ADO immediately after alkane release. Our study will be useful in improving the efficiency of bioalkane production using AAR and ADO.
蓝藻细菌可以通过一个涉及酰基-(酰基载体蛋白)还原酶(AAR)和醛脱甲酰基加氧酶(ADO)的两步酶促过程来生产与柴油相当的烷烃,这提供了一种潜在的可再生生物燃料来源。AAR与ADO结合以有效传递醛底物,并且有人提出当烷烃产物从与ADO底物入口相同的位点释放时它们会解离。然而,在底物进入和产物释放过程中ADO内底物和产物的动态变化却知之甚少。在这里,我们对存在底物或产物情况下的ADO进行了分子动力学(MD)模拟。我们发现,虽然醛底物在催化之前保持靠近ADO的活性中心,但烷烃产物在催化后可以在ADO内部的疏水通道内动态旋转,朝着产物出口移动。此外,对ADO以及AAR/ADO复合物进行的平行级联选择(PaCS)-MD模拟确定了底物入口的位置以及ADO上产物释放的多个出口。令人惊讶的是,PaCS-MD模拟显示烷烃产物可以从与底物入口不同的出口释放,而AAR不会解离。基于这些结果,我们提出了一个由AAR/ADO复合物高效生产烷烃的反应模型,其中醛和烷烃在AAR和ADO保持结合的同时被同时合成,并且醛底物可以在烷烃释放后立即被传递到ADO。我们的研究将有助于提高使用AAR和ADO生产生物烷烃的效率。