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Time-Resolved Evolution of Short- and Long-Range Order During the Transformation of Amorphous Calcium Carbonate to Calcite in the Sea Urchin Embryo

机译:海胆胚胎中无定形碳酸钙向方解石转化过程中短程和长程的时间分辨演化

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摘要

Use of amorphous precursors is a widespread strategy in biomineralization. In sea urchin embryos, controlled transformation of amorphous calcium carbonate (ACC) to calcite results in smoothly curving and branching single crystals. However, the mechanism of the disorder-to-order transformation remains poorly understood. Here, the use of strontium as a probe in X-ray absorption spectroscopy (XAS) greatly facilitates investigation of the evolution of order. In pulse-chase experiments, embryos incorporate Sr~(2+) from Sr-enriched seawater into small volumes of the growing endoskeleton. During the chase, the Sr-labeled mineral matures under physiological conditions. Based on Sr K-edge spectra of cryo-frozen whole embryos, it is proposed that the transformation occurs in three stages. The initially deposited calcium carbonate has short-range order resembling synthetic hydrated ACC. Within 3 h, the short-range order of calcite is established. Between 3 h and 24 h, the short-range order does not change, while long-range order increases. These results refute the notion that organisms imprint the local order of the final crystal on ACC. Furthermore, it is proposed that the intermediate is more similar to disordered calcite than to anhydrous ACC. Pulse-chase experiments in conjunction with heavy element labeling have great potential to improve understanding of phase transformations during biomineralization.
机译:非晶态前体的使用是生物矿化中的广泛策略。在海胆胚胎中,无定形碳酸钙(ACC)向方解石的受控转变导致单晶平滑弯曲和分支。然而,从无序到有序转化的机制仍然知之甚少。在此,将锶用作X射线吸收光谱法(XAS)中的探针极大地促进了有序演化的研究。在脉冲追踪实验中,胚胎将富含Sr的海水中的Sr〜(2+)掺入少量的生长中的内骨骼中。在追赶过程中,Sr标记的矿物质会在生理条件下成熟。基于冷冻冷冻全胚的Sr K-edge光谱,提出了转化过程分为三个阶段。最初沉积的碳酸钙具有类似于合成水合ACC的短程有序。在3小时内,方解石的短程建立。在3小时到24小时之间,短距离顺序不会改变,而长距离顺序会增加。这些结果驳斥了生物体将最终晶体的局部顺序印在ACC上的观点。此外,提出该中间体与无序方解石比与无水ACC更相似。脉冲追踪实验与重元素标记相结合,具有巨大的潜力,可以增进对生物矿化过程中相变的理解。

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  • 来源
    《Advanced Functional Materials》 |2013年第34期|4185-4194|共10页
  • 作者单位

    Department of Materials Science and Engineering Northwestern University Evanston, IL 60208, USA;

    Department of Materials Science and Engineering Northwestern University Evanston, IL 60208, USA;

    Department of Materials Science and Engineering Northwestern University Evanston, IL 60208, USA;

    Department of Materials Science and Engineering Northwestern University Evanston, IL 60208, USA;

    Department of Materials Science and Engineering Northwestern University Evanston, IL 60208, USA;

    Advanced Photon Source Argonne National Laboratory Argonne, IL 60439, USA;

    Advanced Photon Source Argonne National Laboratory Argonne, IL 60439, USA;

    Advanced Photon Source Argonne National Laboratory Argonne, IL 60439, USA;

    Advanced Photon Source Argonne National Laboratory Argonne, IL 60439, USA;

    Department of Materials Science and Engineering Northwestern University Evanston, IL 60208, USA;

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