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首页> 外文期刊>Advanced Functional Materials >Particle Accretion Mechanism Underlies Biological Crystal Growth from an Amorphous Precursor Phase
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Particle Accretion Mechanism Underlies Biological Crystal Growth from an Amorphous Precursor Phase

机译:粒子积聚机制是非晶态前体相生物晶体生长的基础

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Many biogenic minerals are composed of aggregated particles at the nanoscale. These minerals usually form through the transformation of amorphous precursors into single crystals inside a privileged space controlled by the organism. Here, in vitro experiments aimed at understanding the factors responsible for producing such single crystals with aggregated particle texture are presented. Crystallization is achieved by a two-step reaction in which amorphous calcium carbonate (ACC) is first precipitated and then transformed into calcite in small volumes of water and in the presence of additives. The additives used are gel-forming molecules, phosphate ions, and the organic extract from sea urchin embryonic spicules - all are present in various biogenic crystals that grow via the transformation of ACC. Remarkably, this procedure yields faceted single-crystals of calcite that maintain the nanoparticle texture. The crystals grow predominantly by the accretion of ACC nanoparticles, which subsequently crystallize. Gels and phosphate ions stabilize ACC via a different mechanism than sea urchin spicule macromolecules. It is concluded that the unique nanoparticle texture of biogenic minerals results from formation pathways that may differ from one another, but given the appropriate precursor and micro-environment, share a common particle accretion mechanism.
机译:许多生物矿物由纳米级的聚集颗粒组成。这些矿物通常是在有机体控制的特权空间内,通过将无定形前体转变为单晶而形成的。在这里,提出了旨在理解造成具有聚集的颗粒质地的单晶的因素的体外实验。结晶是通过两步反应实现的,其中先沉淀无定形碳酸钙(ACC),然后在少量水和添加剂存在下将其转化为方解石。所使用的添加剂是形成凝胶的分子,磷酸根离子和海胆胚胎针状体的有机提取物-它们都存在于通过ACC转化而生长的各种生物晶体中。显着地,该程序产生了方解石的多面单晶,其保持了纳米颗粒的质地。晶体主要通过ACC纳米颗粒的积聚而生长,随后会结晶。凝胶和磷酸根离子通过与海胆针状大分子不同的机制来稳定ACC。结论是,生物矿物质的独特纳米颗粒质地是由可能彼此不同的形成途径产生的,但是在适当的前体和微环境下,它们具有共同的颗粒积聚机制。

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  • 来源
    《Advanced Functional Materials 》 |2014年第34期| 5420-5426| 共7页
  • 作者单位

    Dept. of Structural Biology Weizmann Institute of Science Rehovot 76100, Israel;

    Dept. of Structural Biology Weizmann Institute of Science Rehovot 76100, Israel;

    Dept. of Structural Biology Weizmann Institute of Science Rehovot 76100, Israel;

    Dept. of Physics University of Wisconsin-Madison 1150 University Avenue Madison, WI 53706, USA;

    Dept. of Physics University of Wisconsin-Madison 1150 University Avenue Madison, WI 53706, USA,Dept. of Chemistry University of Wisconsin-Madison 1101 University Avenue Madison, WI 53706, USA;

    Dept. of Biomaterials Max Planck Institute of Colloids and Interfaces 14424 Potsdam, Germany;

    Dept. of Structural Biology Weizmann Institute of Science Rehovot 76100, Israel;

    Dept. of Structural Biology Weizmann Institute of Science Rehovot 76100, Israel;

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