A crucial process: organic matrix and magnesium ion control of amorphous calcium carbonate crystallization on β-chitin film

CrystEngComm ◽  
2015 ◽  
Vol 17 (1) ◽  
pp. 32-39 ◽  
Author(s):  
Yufei Ma ◽  
Qingling Feng

ACC transformation processes occurring on chitin film mediated by a water soluble matrix or magnesium ions in aqueous solution were investigated.

2010 ◽  
Vol 22 (1) ◽  
pp. 161-166 ◽  
Author(s):  
Yael Politi ◽  
David R. Batchelor ◽  
Paul Zaslansky ◽  
Bradley F. Chmelka ◽  
James C. Weaver ◽  
...  

2013 ◽  
Vol 117 (47) ◽  
pp. 14849-14856 ◽  
Author(s):  
Hidekazu Tomono ◽  
Hiroki Nada ◽  
Fangjie Zhu ◽  
Takeshi Sakamoto ◽  
Tatsuya Nishimura ◽  
...  

2008 ◽  
Vol 72 (1) ◽  
pp. 243-246 ◽  
Author(s):  
Y. Dauphin

AbstractCalcite and aragonite shell layers of the main classes of Molluscs are composed of monocrystalline units (prisms, tablets, laths or fibres). Scanning electron and atomic force microscopy studies show these units are composed of small round granules with a thin cortex (amorphous calcium carbonate and/or organic matrix). These granules are organo-mineral composites. A comparison of the size and shape of the granules in different taxa (Mollusca, Brachiopoda) suggests a possible relationship with taxonomy and/or phylogeny.


2020 ◽  
Vol 128 (8) ◽  
pp. 560-564
Author(s):  
Yuta SHUSEKI ◽  
Fumihiro MIHARA ◽  
Atsuo YASUMORI ◽  
Yasushi IDEMOTO ◽  
Setsuko KOURA ◽  
...  

2016 ◽  
Vol 672 ◽  
pp. 47-59 ◽  
Author(s):  
Stephan E. Wolf ◽  
Corinna Böhm ◽  
Joe Harris ◽  
Myriam Hajir ◽  
Mihail Mondeshki ◽  
...  

We revisit the ultrastructural features of different calcareous biominerals and identify remarkable similarities: taxonomically very distant species show a common nanogranular structure, even if different extracellular secretion patterns are employed or calcium carbonate polymorphs formed. By these analyses, we elucidate the locus of the small fraction of intracrystalline organic matrix revealing its intergranular character and localize the intracrystalline amorphous calcium carbonate moiety commonly found in mesocrystalline biominerals and provide a first explanation for the pathway by which it is preserved.


Science ◽  
2019 ◽  
Vol 363 (6425) ◽  
pp. 396-400 ◽  
Author(s):  
Zhaoyong Zou ◽  
Wouter J. E. M. Habraken ◽  
Galina Matveeva ◽  
Anders C. S. Jensen ◽  
Luca Bertinetti ◽  
...  

As one of the most abundant materials in the world, calcium carbonate, CaCO3, is the main constituent of the skeletons and shells of various marine organisms. It is used in the cement industry and plays a crucial role in the global carbon cycle and formation of sedimentary rocks. For more than a century, only three polymorphs of pure CaCO3—calcite, aragonite, and vaterite—were known to exist at ambient conditions, as well as two hydrated crystal phases, monohydrocalcite (CaCO3·1H2O) and ikaite (CaCO3·6H2O). While investigating the role of magnesium ions in crystallization pathways of amorphous calcium carbonate, we unexpectedly discovered an unknown crystalline phase, hemihydrate CaCO3·½H2O, with monoclinic structure. This discovery may have important implications in biomineralization, geology, and industrial processes based on hydration of CaCO3.


2019 ◽  
Author(s):  
Nancy Watfa ◽  
Weimin Xuan ◽  
Zoe Sinclair ◽  
Robert Pow ◽  
Yousef Abul-Haija ◽  
...  

Investigations of chiral host guest chemistry are important to explore recognition in confined environments. Here, by synthesizing water-soluble chiral porous nanocapsule based on the inorganic metal-oxo Keplerate-type cluster, {Mo<sub>132</sub>} with chiral lactate ligands with the composition [Mo<sub>132</sub>O<sub>372</sub>(H<sub>2</sub>O)<sub>72</sub>(<i>x-</i>Lactate)<sub>30</sub>]<sup>42-</sup> (<i>x</i> = D or L), it was possible to study the interaction with a chiral guest, L/D-carnitine and (<i>R</i>/<i>S</i>)-2-butanol in aqueous solution. The enantioselective recognition was studied by quantitative <sup>1</sup>H NMR and <sup>1</sup>H DOSY NMR which highlighted that the chiral recognition is regulated by two distinct sites. Differences in the association constants (K) of L- and D-carnitine, which, due to their charge, are generally restricted from entering the interior of the host, are observed, indicating that their recognition predominantly occurs at the surface pores of the structure. Conversely, a larger difference in association constants (K<i><sub>S</sub></i>/K<i><sub>R</sub></i> = 3) is observed for recognition within the capsule interior of (<i>R</i>)- and (<i>S</i>)-2-butanol.


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