MRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge Biomedical Campus, Cambridge, CB2 0QH, UK.
Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge, CB2 1EW, UK.
Nat Commun. 2018 May 8;9(1):1821. doi: 10.1038/s41467-018-04147-2.
When considering life's aetiology, the first questions that must be addressed are "how?" and "where?" were ostensibly complex molecules, considered necessary for life's beginning, constructed from simpler, more abundant feedstock molecules on primitive Earth. Previously, we have used multiple clues from the prebiotic synthetic requirements of (proto)biomolecules to pinpoint a set of closely related geochemical scenarios that are suggestive of flow and semi-batch chemistries. We now wish to report a multistep, uninterrupted synthesis of a key heterocycle (2-aminooxazole) en route to activated nucleotides starting from highly plausible, prebiotic feedstock molecules under conditions which mimic this scenario. Further consideration of the scenario has uncovered additional pertinent and novel aspects of prebiotic chemistry, which greatly enhance the efficiency and plausibility of the synthesis.
在考虑生命的病因学时,必须首先解决的问题是“如何?”和“何处?”原本复杂的分子,被认为是生命起源所必需的,是由原始地球上更简单、更丰富的原料分子构建而成。在此之前,我们已经使用了(原)生物分子前生物合成要求的多个线索,来确定一组密切相关的地球化学情景,这些情景表明存在流动和半分批化学。现在,我们希望报告在模拟该情景的条件下,从高度合理的前生物原料分子出发,通过多步、不间断的合成,从关键的杂环(2-氨基恶唑)到激活核苷酸的合成。进一步考虑该情景揭示了前生物化学的其他相关和新颖方面,极大地提高了合成的效率和合理性。