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在双金属钴 - 镍纳米结构上由甲酸盐进行微滴的益生元合成。

Prebiotic Synthesis of Microdroplets from Formate over a Bimetallic Cobalt-Nickel Nanomotif.

作者信息

Zhu Peidong, Wang Chunling, Lang Junyu, He Daoping, Jin Fangming

机构信息

School of Environmental Science and Engineering, State Key Laboratory of Metal Matrix Composites, Shanghai Jiao Tong University, Shanghai 200240, China.

School of Physical Science and Technology, ShanghaiTech University, Shanghai 201210, China.

出版信息

J Am Chem Soc. 2024 Sep 11;146(36):25005-25015. doi: 10.1021/jacs.4c06989. Epub 2024 Sep 1.

Abstract

The hypothesis underlying the abiogenic origin of life suggests that the nonenzymatic synthesis of long-chain fatty acids led to the construction of vesicles for compartmentalization in an early stage during the transition from geochemistry to biochemistry. However, evidence for this theory remains elusive as C carboxylic acids cannot be synthesized using current laboratory simulations. Here, we report the synthesis of long-chain carboxylic acids (C-C) with a 42 mmol/g yield and 87.7% selectivity from formate (an intermediate of the acetyl-CoA pathway) over a cobalt-nickel alloy under alkaline hydrothermal conditions and the subsequent formation of microdroplets from organics. Density functional theory (DFT) calculations confirmed that the synergistic effect of the bimetal catalyst is key for catalyzing C-C coupling. Investigations by infrared spectroscopy, electron paramagnetic resonance, and isotope-labeled experiments revealed that HCO* serves as a reaction intermediate and is involved in the subsequent elementary steps for synthesizing long-chain carboxylic acids from formate. Taken together, these findings may help explain how the first protocells emerged geochemically and provide support for the hypothesis of the abiogenic origin of life. The hydrothermal system developed may also be applicable for the sustainable synthesis of long-chain carboxylates from one-carbon substrates using nonnoble metal catalysts.

摘要

生命非生物起源的潜在假设表明,长链脂肪酸的非酶促合成导致在从地球化学向生物化学转变的早期阶段构建用于区室化的囊泡。然而,由于目前的实验室模拟无法合成C羧酸,该理论的证据仍然难以捉摸。在此,我们报告了在碱性水热条件下,长链羧酸(C-C)从甲酸盐(乙酰辅酶A途径的中间体)以42 mmol/g的产率和87.7%的选择性在钴镍合金上合成,以及随后从有机物形成微滴。密度泛函理论(DFT)计算证实,双金属催化剂的协同作用是催化C-C偶联的关键。通过红外光谱、电子顺磁共振和同位素标记实验的研究表明,HCO*作为反应中间体,并参与从甲酸盐合成长链羧酸的后续基本步骤。综上所述,这些发现可能有助于解释第一批原始细胞是如何在地球化学上出现的,并为生命非生物起源的假设提供支持。所开发的水热系统也可能适用于使用非贵金属催化剂从单碳底物可持续合成长链羧酸盐。

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