

FOLLOWUS
1. College of Chemical and Environmental Engineering Shandong University of Science and Technology
2. Shandong Provincial Key Laboratory of Depositional Mineralization and Sedimentary Minerals College of Geological Science and Engineering Shandong University of Science and Technology
3. State Key Laboratory of Mining Disaster Prevention and Control Shandong University of Science & Technology
4. Yantai Institute of Coastal Zone Research Chinese Academy of Sciences
网络首发:2013-10-29,
纸质出版:2014
Scan QR Code
Characterization of calcium deposition induced by Synechocystis sp. PCC6803 in BG11 culture medium[J]. 海洋湖沼学报(英文), 2014,32(3):503-510.
Yan, H., Han, Z., Zhao, H. et al. Characterization of calcium deposition induced by Synechocystis sp. PCC6803 in BG11 culture medium., Chin. J. Ocean. Limnol. 32, 503–510 (2014). https://doi.org/10.1007/s00343-014-3150-2
Characterization of calcium deposition induced by Synechocystis sp. PCC6803 in BG11 culture medium[J]. 海洋湖沼学报(英文), 2014,32(3):503-510. DOI: 10.1007/s00343-014-3150-2.
Yan, H., Han, Z., Zhao, H. et al. Characterization of calcium deposition induced by Synechocystis sp. PCC6803 in BG11 culture medium., Chin. J. Ocean. Limnol. 32, 503–510 (2014). https://doi.org/10.1007/s00343-014-3150-2 DOI:
Calcium carbonate (CaCO3) crystals in their preferred orientation were obtained in BG11 culture media inoculated with Synechocystis sp. PCC6803 (inoculated BG11). In this study
the features of calcium carbonate deposition were investigated. Inoculated BG11 in different calcium ion concentrations was used for the experimental group
while the BG11 culture medium was used for the control group. The surface morphologies of the calcium carbonate deposits in the experimental and control groups were determined by scanning and transmission electron microscopy. The deposits were analyzed by electronic probe micro-analysis
Fourier transform infrared spectrum
X-ray diffraction
thermal gravimetric analysis and differential scanning calorimetry. The results show that the surfaces of the crystals in the experimental group were hexahedral in a scaly pattern. The particle sizes were micrometer-sized and larger than those in the control group. The deposits of the control group contained calcium (Ca)
carbon (C)
oxygen (O)
phosphorus (P)
iron (Fe)
copper (Cu)
zinc (Zn)
and other elements. The deposits in the experimental group contained Ca
C
and O only. The deposits of both groups contained calcite. The thermal decomposition temperature of the deposits in the control group was lower than those in the experimental group. It showed that the CaCO3 deposits of the experimental group had higher thermal stability than those of the control group. This may be due to the secondary metabolites produced by the algae cells
which affect the carbonate crystal structure and result in a close-packed structure. The algae cells that remained after thermal weight loss were heavier in higher calcium concentrations in BG11 culture media. There may be more calcium-containing crystals inside and outside of these cells. These results shall be beneficial for understanding the formation mechanism of carbonate minerals.
Cacchio P, Ercole C, Cappuccio G, Lepidi A. 2003. Calcium carbonate precipitation by bacterial strains isolated from a limestone cave and from a loamy soil. Geomicrobiol. J., 20: 85–95.
Castanier S, Le Métayer-Levrel G, Perthuisot J P. 1999. Cacarbonates precipitation and limestone genesis—the microbiologist point of view. Sediment. Geol., 126: 9–23.
CŌlfen H. 2003. Precipitation of carbonates: recent progress in controlled production of complex shapes. Curr. Opin. Colloid Interface Sci., 8: 23–31.
de Vrind-de Jong E W, de Vrind J P M. 1997. Algal deposition of carbonates and silicates. In: Banfield J F, Nealson K H eds. Geomicrobiology: Interactions Between Microbes and Minerals, 35. Mineralogical Society of America, Washington, DC. p.267–307.
Dittrich M, Kurz P, Wehrli B. 2004. The role of autotrophic picocyanobacteria in calcite precipitation in an oligotrophic lake. Geomicrobiol. J., 21: 45–53.
Dittrich M, Muller B, Mavrocordatos D, Wehrli B. 2003. Induced calcite precipitation by cyanobacterium Synechococcus. Acta Hydrochim. Hydrobiol., 31: 162–169.
Fujita Y, Ferris F G, Lawson R D, Colwell F S, Smith R W. 2000. Calcium carbonate precipitation by ureolytic subsurface bacteria. Geomicrobiol. J., 17: 305–318.
Hammes F, Boon N, de Villiers J, Verstraete W, Siciliano S D. 2003. Strain-specific ureolytic microbial calcium carbonate precipitation. Appl. Environ. Microbiol., 69: 4 901–4 909.
Hammes F, Verstraete W. 2002. Key roles of pH and calcium metabolism in microbial carbonate precipitation. Rev. Environ. Sci. Biotechnol., 1: 3–7.
Han Z Z, Yan H X, Zhou S X, Zhao H, Zhang Y, Zhang N N, Yao C K, Zhao L, Han C Y. 2013. Precipitation of calcite induced by Synechocystis sp. PCC6803. World J. Microbiol. Biotechnol., http://dx.doi.org/10.1007/s11274-013-1341-1.
Kimura T, Koga N. 2011. Thermal dehydration of monohydrocalcite: overall kinetics and physicogeometrical mechanisms. J. Phys. Chem. A, 115: 10 491–10 501.
Lee B D, Apel W A, Walton M R. 2006. Calcium carbonate formation by Synechococcus sp. strain PCC8806 and Synechococcus sp. strain PCC8807. Bioresour. Technol., 97: 2 427–2 434.
Liu Y Y, Jiang J, Gao M R, Yu B, Mao L B, Yu S H. 2013. Phase transformation of magnesium amorphous calcium carbonate (Mg-ACC) in a binary solution of ethanol and water. Cryst. Growth Des., 13: 59–65.
Manoli F, Dalas E. 2000. Spontaneous precipitation of calcium carbonate in the presence of chondroitin sulfate. J. Cryst. Growth, 217: 416–421.
Milliman J D, Troy P J, Balch W M, Adams A K, Li Y H, Mackenzie F T. 1999. Biologically mediated dissolution of calcium carbonate above the chemical lysocline? Deep — Sea Res., 46: 1 653–1 669.
Ren D N, Feng Q L, Bourrat X. 2011. Effects of additives and templates on calcium carbonate mineralization in vitro. Chin. J. Oceanol. Limnol., 42: 228–245.
Rippka R, Deruelles J, Waterbury J, Herdman M, Stanier R. 1979. Generic assignments, strain histories and properties of pure cultures of cyanobacteria. J. Gen. Microbiol., 111: 1–61.
Spanos N, Koutsoukos P G. 1998. The transformation of vaterite to calcite: effect of the conditions of the solution in contact with the mineral phase. J. Cryst. Growth, 191: 783–90.
Tong H, Ma W T, Wang L L, Wan P, Hu J M, Cao L X. 2004. Control over the crystal phase, shape, size and aggregation of calcium carbonate via an L-aspartic acid inducing process. Biomaterials, 25: 3 923–3 929.
Yeager C M, Milliken C E, Bagwell C E, Staples L, Berseth P A, Sessions H T. 2011. Evaluation of experimental conditions that influence hydrogen production among heterocystous Cyanobacteria. Int. J. Hydrogen Energy, 36: 7 487–7 499.
0
浏览量
0
Downloads
18
CSCD
关联资源
相关文章
相关作者
相关机构

京公网安备11010802024621