Martin William, Russell Michael J
Institute of Botany, University of Düsseldorf, 40225 Düsseldorf, Germany.
Philos Trans R Soc Lond B Biol Sci. 2007 Oct 29;362(1486):1887-925. doi: 10.1098/rstb.2006.1881.
A model for the origin of biochemistry at an alkaline hydrothermal vent has been developed that focuses on the acetyl-CoA (Wood-Ljungdahl) pathway of CO2 fixation and central intermediary metabolism leading to the synthesis of the constituents of purines and pyrimidines. The idea that acetogenesis and methanogenesis were the ancestral forms of energy metabolism among the first free-living eubacteria and archaebacteria, respectively, stands in the foreground. The synthesis of formyl pterins, which are essential intermediates of the Wood-Ljungdahl pathway and purine biosynthesis, is found to confront early metabolic systems with steep bioenergetic demands that would appear to link some, but not all, steps of CO2 reduction to geochemical processes in or on the Earth's crust. Inorganically catalysed prebiotic analogues of the core biochemical reactions involved in pterin-dependent methyl synthesis of the modern acetyl-CoA pathway are considered. The following compounds appear as probable candidates for central involvement in prebiotic chemistry: metal sulphides, formate, carbon monoxide, methyl sulphide, acetate, formyl phosphate, carboxy phosphate, carbamate, carbamoyl phosphate, acetyl thioesters, acetyl phosphate, possibly carbonyl sulphide and eventually pterins. Carbon might have entered early metabolism via reactions hardly different from those in the modern Wood-Ljungdahl pathway, the pyruvate synthase reaction and the incomplete reverse citric acid cycle. The key energy-rich intermediates were perhaps acetyl thioesters, with acetyl phosphate possibly serving as the universal metabolic energy currency prior to the origin of genes. Nitrogen might have entered metabolism as geochemical NH3 via two routes: the synthesis of carbamoyl phosphate and reductive transaminations of alpha-keto acids. Together with intermediates of methyl synthesis, these two routes of nitrogen assimilation would directly supply all intermediates of modern purine and pyrimidine biosynthesis. Thermodynamic considerations related to formyl pterin synthesis suggest that the ability to harness a naturally pre-existing proton gradient at the vent-ocean interface via an ATPase is older than the ability to generate a proton gradient with chemistry that is specified by genes.
一种关于碱性热液喷口处生物化学起源的模型已经建立,该模型聚焦于二氧化碳固定的乙酰辅酶A(伍德-Ljungdahl)途径以及通向嘌呤和嘧啶成分合成的中心中间代谢。产乙酸作用和产甲烷作用分别是最早的自由生活真细菌和古细菌中能量代谢的祖先形式这一观点处于突出地位。发现甲酰蝶呤的合成,它是伍德-Ljungdahl途径和嘌呤生物合成的关键中间体,使早期代谢系统面临巨大的生物能量需求,这似乎将二氧化碳还原的一些(但不是全部)步骤与地壳内或地壳上的地球化学过程联系起来。考虑了现代乙酰辅酶A途径中依赖蝶呤的甲基合成所涉及的核心生化反应的无机催化益生元类似物。以下化合物似乎是益生元化学中可能起核心作用的候选物:金属硫化物、甲酸、一氧化碳、甲硫醚、乙酸、甲酰磷酸、羧基磷酸、氨基甲酸酯、氨基甲酰磷酸、乙酰硫酯、乙酰磷酸、可能还有羰基硫以及最终的蝶呤。碳可能通过与现代伍德-Ljungdahl途径、丙酮酸合酶反应和不完全反向柠檬酸循环中几乎没有差异的反应进入早期代谢。关键的富含能量的中间体可能是乙酰硫酯,在基因起源之前,乙酰磷酸可能作为通用的代谢能量货币。氮可能通过两条途径作为地球化学的氨进入代谢:氨基甲酰磷酸的合成和α-酮酸的还原性转氨作用。与甲基合成的中间体一起,这两条氮同化途径将直接提供现代嘌呤和嘧啶生物合成的所有中间体。与甲酰蝶呤合成相关的热力学考虑表明,通过ATP酶利用喷口-海洋界面处自然存在的质子梯度的能力比利用由基因指定的化学反应产生质子梯度的能力更古老。