Patel Bhavesh H, Percivalle Claudia, Ritson Dougal J, Duffy Colm D, Sutherland John D
MRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge Biomedical Campus, Cambridge CB2 0QH, UK.
Nat Chem. 2015 Apr;7(4):301-7. doi: 10.1038/nchem.2202. Epub 2015 Mar 16.
A minimal cell can be thought of as comprising informational, compartment-forming and metabolic subsystems. To imagine the abiotic assembly of such an overall system, however, places great demands on hypothetical prebiotic chemistry. The perceived differences and incompatibilities between these subsystems have led to the widely held assumption that one or other subsystem must have preceded the others. Here we experimentally investigate the validity of this assumption by examining the assembly of various biomolecular building blocks from prebiotically plausible intermediates and one-carbon feedstock molecules. We show that precursors of ribonucleotides, amino acids and lipids can all be derived by the reductive homologation of hydrogen cyanide and some of its derivatives, and thus that all the cellular subsystems could have arisen simultaneously through common chemistry. The key reaction steps are driven by ultraviolet light, use hydrogen sulfide as the reductant and can be accelerated by Cu(I)-Cu(II) photoredox cycling.
最小细胞可以被认为是由信息、形成区室和代谢子系统组成。然而,要设想这样一个整体系统的非生物组装,对假设的前生物化学提出了很高的要求。这些子系统之间明显的差异和不相容性导致了一种广泛持有的假设,即其中一个或其他子系统必定先于其他子系统出现。在这里,我们通过研究从具有前生物合理性的中间体和一碳原料分子组装各种生物分子构件,来实验性地研究这一假设的有效性。我们表明,核糖核苷酸、氨基酸和脂质的前体都可以通过氰化氢及其一些衍生物的还原同系化得到,因此所有细胞子系统可能通过共同的化学过程同时出现。关键反应步骤由紫外线驱动,使用硫化氢作为还原剂,并且可以通过Cu(I)-Cu(II)光氧化还原循环加速。