Monte Marisa B M, Duarte Ana C P, Bonapace José A P, Do Amaral Manoel R, Vieyra Adalberto, De Souza-Barros Fernando
Centro de Tecnologia Mineral (CETEM), Ministério da Ciência e da Tecnologia, Rio de Janeiro, Brasil.
Orig Life Evol Biosph. 2003 Feb;33(1):37-52. doi: 10.1023/a:1023974424070.
The present study is based on the proposal that if the aqueous phosphorus-capture mechanism by iron oxide precursors was inhibited in prebiotic anoxic scenarios then soluble phosphates could have been more available than what is observed now. Supporting this conjecture, we examine prevailing contemporary trapping mechanisms of orthophosphate (Pi) and pyrophosphate (PPi). To illustrate its efficiency, the attachment of (Pi) onto aggregates of iron-3 oxyhydroxide is compared with the one reported for the product of its condensation, PPi. The electrophoretic profiles of the Pi- and PPi-aggregate complexes reveal different pH-modulated interactions of the phosphorylated compounds with both the aggregate and its aqueous surrounding layers. The observed differences of Pi/PPi sorption and desorption mechanisms are discussed in terms of their consequences to the prebiotic availability of soluble orthophosphate and of a phosphorylated compound having the high-energy phosphoanhydride linkage and a molecule representative of condensed oligophosphates.
在益生元缺氧环境中,如果氧化铁前体的水相磷捕获机制受到抑制,那么可溶性磷酸盐的可利用性可能会比目前观察到的更高。为支持这一推测,我们研究了当前普遍存在的正磷酸盐(Pi)和焦磷酸盐(PPi)的捕获机制。为说明其效率,将(Pi)附着到氢氧化铁 - 3聚集体上的情况与报道的其缩合产物PPi的情况进行了比较。Pi - 和PPi - 聚集体复合物的电泳图谱揭示了磷酸化化合物与聚集体及其水相周围层之间不同的pH调节相互作用。从它们对可溶性正磷酸盐、具有高能磷酐键的磷酸化化合物以及缩合寡磷酸盐分子的益生元可利用性的影响方面,讨论了观察到的Pi/PPi吸附和解吸机制的差异。