Pontes-Buarque M, Tessis AC, Bonapace JA, Monte MB, Souza-Barros FD, Vieyra A
Instituto de Biofisica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, 21941-590, Brazil.
An Acad Bras Cienc. 2000 Sep;72(3):317-22. doi: 10.1590/s0001-37652000000300005.
There exists an extensive literature on the possible roles of minerals in the prebiotic stages of the chemical evolution of life (Bernal 1951, Cairns-Smith 1982, Wachtershauser 1992, Vieyra et al. 1995, Tessis et al. 1999, see Lahav (1994) for a review). Among the original proposals, minerals have been considered in: (a) processes that would discriminate molecular chirality; (b) condensation reactions of biomolecular precursors; (c) prebiotic catalysis; (d) biochemical templates; and (e) autocatalytic metabolism. In this communication it is emphazised the complex properties of both surface reactions and interfaces between minerals and aqueous solutions simulating Archean scenarios. The properties of pyrite surface net charge and of its interface with a solution simulating primitive seawater are discussed and their implications to the autocatalytic model (Wachtershauser 1988a 1992) are presented in order to demonstrate their relevance. The proposed roles of iron-sulfide minerals (mainly pyrite) as physical support for primitive bidimensional metabolism and chiral discriminator (Wachtershauser 1988a, Huber & Wachtershauser 1998) are revised. It is shown that: (a) the net surface charge can be modulated by the pyrite-aqueous solution interface; (b) mononucleotides attachment to pyrite require a cationic bridge; and (c) direct absorption of acetate - a molecule proposed as carbon source in primitive aqueous environments - also modulates the interface properties and would have masked pyrite's bulk structure. These results indicate that physicochemical changes of mineral surfaces - caused by environments simulating Archean aqueous scenarios - should be taken into account in the proposals of mineral prebiotic roles.
关于矿物质在生命化学演化的前生物阶段可能发挥的作用,已有大量文献(伯纳尔,1951年;凯恩斯 - 史密斯,1982年;瓦赫特绍伊泽,1992年;维埃拉等人,1995年;泰西斯等人,1999年;有关综述见拉哈夫,1994年)。在最初的提议中,矿物质被认为参与了以下方面:(a)区分分子手性的过程;(b)生物分子前体的缩合反应;(c)前生物催化;(d)生化模板;以及(e)自催化代谢。在本通讯中,强调了模拟太古宙情景的矿物质与水溶液之间表面反应和界面的复杂特性。讨论了黄铁矿表面净电荷及其与模拟原始海水溶液界面的性质,并阐述了它们对自催化模型(瓦赫特绍伊泽,1988a,1992年)的影响,以证明其相关性。对硫化铁矿物质(主要是黄铁矿)作为原始二维代谢的物理支撑和手性鉴别器(瓦赫特绍伊泽,1988a;胡贝尔和瓦赫特绍伊泽,1998年)所提出的作用进行了修订。结果表明:(a)黄铁矿 - 水溶液界面可调节表面净电荷;(b)单核苷酸附着于黄铁矿需要阳离子桥;(c)在原始水环境中被提议作为碳源的醋酸盐分子的直接吸附,也会调节界面性质,并可能掩盖黄铁矿的整体结构。这些结果表明,在关于矿物质前生物作用的提议中,应考虑模拟太古宙水环境引起的矿物质表面物理化学变化。