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The enzyme carbonic anhydrase as an integral component of biogenic Ca-carbonate formation in sponge spicules()
The inorganic scaffold of the spicules, the skeletal elements of the calcareous sponges, is formed of calcium carbonate (CaCO(3)). The growth of the approximately 300-μm large spicules, such as those of the calcareous sponge Sycon raphanus used in the present study, is a rapid process with a rate of...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3821024/ https://www.ncbi.nlm.nih.gov/pubmed/24251096 http://dx.doi.org/10.1016/j.fob.2013.08.004 |
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author | Müller, Werner E.G. Schröder, Heinz C. Schlossmacher, Ute Neufurth, Meik Geurtsen, Werner Korzhev, Michael Wang, Xiaohong |
author_facet | Müller, Werner E.G. Schröder, Heinz C. Schlossmacher, Ute Neufurth, Meik Geurtsen, Werner Korzhev, Michael Wang, Xiaohong |
author_sort | Müller, Werner E.G. |
collection | PubMed |
description | The inorganic scaffold of the spicules, the skeletal elements of the calcareous sponges, is formed of calcium carbonate (CaCO(3)). The growth of the approximately 300-μm large spicules, such as those of the calcareous sponge Sycon raphanus used in the present study, is a rapid process with a rate of about 65 μm/h. The formation of CaCO(3) is predominantly carried out by the enzyme carbonic anhydrase (CA). The enzyme from the sponge S. raphanus was isolated and prepared by recombination. The CA-driven deposition of CaCO(3) crystallites is dependent on temperature (optimal at 52 °C), the pH value of the reaction assay (7.5/8.0), and the substrate concentration (CO(2) and Ca(2+)). During the initial phase of crystallite formation, ≈40 μm large round-shaped deposits are formed that remodel to larger prisms. These crystal-like prisms associate to each other and form either rope-/bundle-like aggregates or arrange perfectly with their smaller planes along opposing surfaces of the sponge spicule rays. The CA-dependent CaCO(3) deposition can be inhibited by the CA-specific inhibitor acetazolamide. The Michaelis–Menten constant for the CA-driven mineralization has been determined to be around 8 mM with respect to CaCO(3). The deposits formed have a Martens hardness of ≈5 GPa. The data presented here highlights for the first time that calcite deposition in the sponge system is decisively controlled enzymatically. This data will contribute to the development of new strategies applicable for the fabrication of novel biomaterials. |
format | Online Article Text |
id | pubmed-3821024 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-38210242013-11-18 The enzyme carbonic anhydrase as an integral component of biogenic Ca-carbonate formation in sponge spicules() Müller, Werner E.G. Schröder, Heinz C. Schlossmacher, Ute Neufurth, Meik Geurtsen, Werner Korzhev, Michael Wang, Xiaohong FEBS Open Bio Article The inorganic scaffold of the spicules, the skeletal elements of the calcareous sponges, is formed of calcium carbonate (CaCO(3)). The growth of the approximately 300-μm large spicules, such as those of the calcareous sponge Sycon raphanus used in the present study, is a rapid process with a rate of about 65 μm/h. The formation of CaCO(3) is predominantly carried out by the enzyme carbonic anhydrase (CA). The enzyme from the sponge S. raphanus was isolated and prepared by recombination. The CA-driven deposition of CaCO(3) crystallites is dependent on temperature (optimal at 52 °C), the pH value of the reaction assay (7.5/8.0), and the substrate concentration (CO(2) and Ca(2+)). During the initial phase of crystallite formation, ≈40 μm large round-shaped deposits are formed that remodel to larger prisms. These crystal-like prisms associate to each other and form either rope-/bundle-like aggregates or arrange perfectly with their smaller planes along opposing surfaces of the sponge spicule rays. The CA-dependent CaCO(3) deposition can be inhibited by the CA-specific inhibitor acetazolamide. The Michaelis–Menten constant for the CA-driven mineralization has been determined to be around 8 mM with respect to CaCO(3). The deposits formed have a Martens hardness of ≈5 GPa. The data presented here highlights for the first time that calcite deposition in the sponge system is decisively controlled enzymatically. This data will contribute to the development of new strategies applicable for the fabrication of novel biomaterials. Elsevier 2013-08-16 /pmc/articles/PMC3821024/ /pubmed/24251096 http://dx.doi.org/10.1016/j.fob.2013.08.004 Text en © 2013 The Authors http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Article Müller, Werner E.G. Schröder, Heinz C. Schlossmacher, Ute Neufurth, Meik Geurtsen, Werner Korzhev, Michael Wang, Xiaohong The enzyme carbonic anhydrase as an integral component of biogenic Ca-carbonate formation in sponge spicules() |
title | The enzyme carbonic anhydrase as an integral component of biogenic Ca-carbonate formation in sponge spicules() |
title_full | The enzyme carbonic anhydrase as an integral component of biogenic Ca-carbonate formation in sponge spicules() |
title_fullStr | The enzyme carbonic anhydrase as an integral component of biogenic Ca-carbonate formation in sponge spicules() |
title_full_unstemmed | The enzyme carbonic anhydrase as an integral component of biogenic Ca-carbonate formation in sponge spicules() |
title_short | The enzyme carbonic anhydrase as an integral component of biogenic Ca-carbonate formation in sponge spicules() |
title_sort | enzyme carbonic anhydrase as an integral component of biogenic ca-carbonate formation in sponge spicules() |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3821024/ https://www.ncbi.nlm.nih.gov/pubmed/24251096 http://dx.doi.org/10.1016/j.fob.2013.08.004 |
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