Chikatani Genta, Nishijima Hiroaki, Ito Yuji, Ikuta Taizo, Nagita Kaito, Tabata Hiro, Harada Takashi, Miyake Rika, Nakanishi Shuji, Hase Yoko
Research Center for Solar Energy Chemistry, Graduate School of Engineering Science, The University of Osaka, Toyonaka, Osaka, Japan.
Toyota Central R&D Labs. Inc., Nagakute, Aichi, Japan.
Commun Chem. 2025 May 30;8(1):166. doi: 10.1038/s42004-025-01560-9.
In biological chemical reactions, substructures formed through multi-step enzymatic reactions organize into large chemical reaction networks (CRNs) that produce complex and sophisticated functions. Recently, significant attention has been paid to artificial, non-enzymatic control of multi-step chemical reactions aimed at synthesizing compounds with structural complexity. However, the synergistic effects arising from the activation of different substructures within a CRN by multiple catalysts remain unexplored. Here we focus on the formose reaction as a non-enzymatic CRN to demonstrate that the complementary activation of multiple substructures by distinct catalysts leads to the emergence of novel functions. Statistical analyses of temporal changes in compound concentrations during reactions catalyzed by γ-AlO and phosphate buffer suggested the presence of a third catalytic species. The experimental results revealed synergistic effects among the substructures activated by γ-AlO, phosphates, and this third species. Our findings demonstrate that multiple catalysts can be designed to control the functions of CRNs.
在生物化学反应中,通过多步酶促反应形成的子结构组织成大型化学反应网络(CRN),这些网络产生复杂而精妙的功能。最近,人们对旨在合成具有结构复杂性的化合物的多步化学反应的人工非酶控制给予了极大关注。然而,多种催化剂对CRN内不同子结构的激活所产生的协同效应仍未得到探索。在这里,我们聚焦于作为非酶CRN的蚁醛反应,以证明不同催化剂对多个子结构的互补激活会导致新功能的出现。对由γ - AlO和磷酸盐缓冲液催化的反应过程中化合物浓度随时间变化的统计分析表明存在第三种催化物质。实验结果揭示了由γ - AlO、磷酸盐和这种第三种物质激活的子结构之间的协同效应。我们的研究结果表明,可以设计多种催化剂来控制CRN的功能。