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首个生命系统:生物能量学视角

The first living systems: a bioenergetic perspective.

作者信息

Deamer D W

机构信息

Department of Chemistry and Biochemistry, University of California, Santa Cruz 95064, USA.

出版信息

Microbiol Mol Biol Rev. 1997 Jun;61(2):239-61. doi: 10.1128/mmbr.61.2.239-261.1997.

Abstract

The first systems of molecules having the properties of the living state presumably self-assembled from a mixture of organic compounds available on the prebiotic Earth. To carry out the polymer synthesis characteristic of all forms of life, such systems would require one or more sources of energy to activate monomers to be incorporated into polymers. Possible sources of energy for this process include heat, light energy, chemical energy, and ionic potentials across membranes. These energy sources are explored here, with a particular focus on mechanisms by which self-assembled molecular aggregates could capture the energy and use it to form chemical bonds in polymers. Based on available evidence, a reasonable conjecture is that membranous vesicles were present on the prebiotic Earth and that systems of replicating and catalytic macromolecules could become encapsulated in the vesicles. In the laboratory, this can be modeled by encapsulated polymerases prepared as liposomes. By an appropriate choice of lipids, the permeability properties of the liposomes can be adjusted so that ionic substrates permeate at a sufficient rate to provide a source of monomers for the enzymes, with the result that nucleic acids accumulate in the vesicles. Despite this progress, there is still no clear mechanism by which the free energy of light, ion gradients, or redox potential can be coupled to polymer bond formation in a protocellular structure.

摘要

具有生命状态特性的首批分子系统大概是由前生物地球上存在的有机化合物混合物自组装而成的。为了进行所有生命形式所特有的聚合物合成,这样的系统将需要一种或多种能量来源来激活要掺入聚合物中的单体。这个过程可能的能量来源包括热、光能、化学能以及跨膜离子电位。本文将探讨这些能量来源,特别关注自组装分子聚集体捕获能量并利用它在聚合物中形成化学键的机制。基于现有证据,一个合理的推测是,膜状囊泡存在于前生物地球上,并且复制和催化大分子系统可能会被包裹在囊泡中。在实验室中,这可以通过制备成脂质体的包封聚合酶来模拟。通过适当选择脂质,可以调节脂质体的通透性,使离子底物以足够的速率渗透,为酶提供单体来源,结果核酸在囊泡中积累。尽管取得了这一进展,但仍然没有明确的机制可以将光、离子梯度或氧化还原电位的自由能与原细胞结构中的聚合物键形成相耦合。

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