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Characterization of organophosphatic brachiopod shells: spectroscopic assessment of collagen matrix and biomineral components

The shells of linguloid brachiopods such as Lingula and Discinisca are inorganic–organic nanocomposites with a mineral phase of calcium phosphate (Ca-phosphate). Collagen, the main extracellular matrix in Ca-phosphatic vertebrate skeletons, has not previously been clearly resolved at the molecular l...

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Autores principales: Agbaje, Oluwatoosin B. A., George, Simon C., Zhang, Zhifei, Brock, Glenn A., Holmer, Lars E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9057340/
https://www.ncbi.nlm.nih.gov/pubmed/35517531
http://dx.doi.org/10.1039/d0ra07523j
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author Agbaje, Oluwatoosin B. A.
George, Simon C.
Zhang, Zhifei
Brock, Glenn A.
Holmer, Lars E.
author_facet Agbaje, Oluwatoosin B. A.
George, Simon C.
Zhang, Zhifei
Brock, Glenn A.
Holmer, Lars E.
author_sort Agbaje, Oluwatoosin B. A.
collection PubMed
description The shells of linguloid brachiopods such as Lingula and Discinisca are inorganic–organic nanocomposites with a mineral phase of calcium phosphate (Ca-phosphate). Collagen, the main extracellular matrix in Ca-phosphatic vertebrate skeletons, has not previously been clearly resolved at the molecular level in organophosphatic brachiopods. Here, modern and recently-alive linguliform brachiopod shells of Lingula and Discinisca have been studied by microRaman spectroscopy, Fourier transform infrared spectroscopy, field emission gun scanning electron microscopy, and thermal gravimetric analysis. For the first time, biomineralized collagen matrix and Ca-phosphate components were simultaneously identified, showing that the collagen matrix is an important moiety in organophosphatic brachiopod shells, in addition to prevalent chitin. Stabilized nanosized apatitic biominerals (up to ∼50 nm) permeate the framework of organic fibrils. There is a ∼2.5-fold higher wt% of carbonate (CO(3)(2−)) in Lingula versus Discinisca shells. Both microRaman spectroscopy and infrared spectra show transient amorphous Ca-phosphate and octacalcium phosphate components. For the first time, trivalent moieties at ∼1660 cm(−1) and divalent moieties at ∼1690 cm(−1) in the amide I spectral region were identified. These are related to collagen cross-links that are abundant in mineralized tissues, and could be important features in the biostructural and mechanical properties of Ca-phosphate shell biominerals. This work provides a critical new understanding of organophosphatic brachiopod shells, which are some of the earliest examples of biomineralization in still-living animals that appeared in the Cambrian radiation.
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spelling pubmed-90573402022-05-04 Characterization of organophosphatic brachiopod shells: spectroscopic assessment of collagen matrix and biomineral components Agbaje, Oluwatoosin B. A. George, Simon C. Zhang, Zhifei Brock, Glenn A. Holmer, Lars E. RSC Adv Chemistry The shells of linguloid brachiopods such as Lingula and Discinisca are inorganic–organic nanocomposites with a mineral phase of calcium phosphate (Ca-phosphate). Collagen, the main extracellular matrix in Ca-phosphatic vertebrate skeletons, has not previously been clearly resolved at the molecular level in organophosphatic brachiopods. Here, modern and recently-alive linguliform brachiopod shells of Lingula and Discinisca have been studied by microRaman spectroscopy, Fourier transform infrared spectroscopy, field emission gun scanning electron microscopy, and thermal gravimetric analysis. For the first time, biomineralized collagen matrix and Ca-phosphate components were simultaneously identified, showing that the collagen matrix is an important moiety in organophosphatic brachiopod shells, in addition to prevalent chitin. Stabilized nanosized apatitic biominerals (up to ∼50 nm) permeate the framework of organic fibrils. There is a ∼2.5-fold higher wt% of carbonate (CO(3)(2−)) in Lingula versus Discinisca shells. Both microRaman spectroscopy and infrared spectra show transient amorphous Ca-phosphate and octacalcium phosphate components. For the first time, trivalent moieties at ∼1660 cm(−1) and divalent moieties at ∼1690 cm(−1) in the amide I spectral region were identified. These are related to collagen cross-links that are abundant in mineralized tissues, and could be important features in the biostructural and mechanical properties of Ca-phosphate shell biominerals. This work provides a critical new understanding of organophosphatic brachiopod shells, which are some of the earliest examples of biomineralization in still-living animals that appeared in the Cambrian radiation. The Royal Society of Chemistry 2020-10-20 /pmc/articles/PMC9057340/ /pubmed/35517531 http://dx.doi.org/10.1039/d0ra07523j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Agbaje, Oluwatoosin B. A.
George, Simon C.
Zhang, Zhifei
Brock, Glenn A.
Holmer, Lars E.
Characterization of organophosphatic brachiopod shells: spectroscopic assessment of collagen matrix and biomineral components
title Characterization of organophosphatic brachiopod shells: spectroscopic assessment of collagen matrix and biomineral components
title_full Characterization of organophosphatic brachiopod shells: spectroscopic assessment of collagen matrix and biomineral components
title_fullStr Characterization of organophosphatic brachiopod shells: spectroscopic assessment of collagen matrix and biomineral components
title_full_unstemmed Characterization of organophosphatic brachiopod shells: spectroscopic assessment of collagen matrix and biomineral components
title_short Characterization of organophosphatic brachiopod shells: spectroscopic assessment of collagen matrix and biomineral components
title_sort characterization of organophosphatic brachiopod shells: spectroscopic assessment of collagen matrix and biomineral components
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9057340/
https://www.ncbi.nlm.nih.gov/pubmed/35517531
http://dx.doi.org/10.1039/d0ra07523j
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