Physics of Living Systems, Massachusetts Institute of Technology, Cambridge, MA 02139.
Blue Marble Space Institute of Science, Seattle, WA, 98154.
Proc Natl Acad Sci U S A. 2022 Apr 5;119(14):e2110787119. doi: 10.1073/pnas.2110787119. Epub 2022 Mar 28.
SignificanceMetabolism relies on a small class of molecules (coenzymes) that serve as universal donors and acceptors of key chemical groups and electrons. Although metabolic networks crucially depend on structurally redundant coenzymes [e.g., NAD(H) and NADP(H)] associated with different enzymes, the criteria that led to the emergence of this redundancy remain poorly understood. Our combination of modeling and structural and sequence analysis indicates that coenzyme redundancy may not be essential for metabolism but could rather constitute an evolved strategy promoting efficient usage of enzymes when biochemical reactions are near equilibrium. Our work suggests that early metabolism may have operated with fewer coenzymes and that adaptation for metabolic efficiency may have driven the rise of coenzyme diversity in living systems.
意义代谢依赖于一小类分子(辅酶),它们作为关键化学基团和电子的通用供体和受体。尽管代谢网络严重依赖于与不同酶相关的结构冗余辅酶[例如 NAD(H) 和 NADP(H)],但导致这种冗余出现的标准仍知之甚少。我们的建模以及结构和序列分析表明,辅酶冗余对于代谢可能不是必需的,而可能是一种进化策略,当生化反应接近平衡时,促进酶的有效利用。我们的工作表明,早期代谢可能使用较少的辅酶,而代谢效率的适应可能导致生命系统中辅酶多样性的增加。