Abnormal Crystallization Sequence of Calcium Carbonate in the Presence of Synechococcus sp. PCC 7942

被引:4
作者
Yang, Guoguo [1 ]
Li, Fuchun [1 ]
Deng, Zelan [1 ]
Wang, Yazhi [1 ]
Su, Zhimeng [1 ]
Huang, Lingjie [1 ]
Yin, Ling [1 ]
Ji, Chen [1 ]
机构
[1] Nanjing Agr Univ, Coll Resources & Environm Sci, Nanjing 210095, Peoples R China
基金
中国国家自然科学基金;
关键词
Crystallization sequence; carbonate mineral; phosphate; extracellular polymeric substances; Synechococcus sp; GROWTH; PRECIPITATION; MORPHOLOGY; CACO3; ARAGONITE; ANHYDRASE; VATERITE;
D O I
10.1080/01490451.2022.2100948
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Studying the crystallization sequence of calcium carbonate (CaCO3) polymorphs provides great insights into bacterial mineralization mechanisms, and carbonate rock genesis in recent geological history. CaCO3 biomineralization studies were conducted using Synechococcus sp. PCC 7942. Changes in bacterial optical density, polysaccharide content, carbonic anhydrase activity, pH, Ca2+, Mg2+, phosphate, and bicarbonate concentrations in medium, and precipitation levels were recorded, while precipitate morphology and polymorphisms were characterized. We identified an abnormal crystallization sequence order of carbonate polymorphs: calcite, aragonite, and vaterite, which failed to obey Ostwald's rule. We investigated saturation indices (SI) and calculated calcite, aragonite, and vaterite quantities. Also, two mineralization studies were performed using PCC 7942 in the medium-plus different phosphates levels and extracellular polymeric substances (EPS) secreted by PCC 7942. Calcite was precipitated due to phosphate levels >7 mu mol center dot L-1 and SIvaterite values 2.3 and phosphate levels <7 mu mol center dot L-1 exerted crucial roles in aragonite formation. Finally, decreased phosphate and Mg2+ levels promoted vaterite crystallization. We suggest this unique crystallization order may be attributed to changes in bacterial density and PO43- levels. Our study provides new insights into bacterial mineralization mechanisms.
引用
收藏
页码:34 / 45
页数:12
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