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Transformation of the matrix structure of shrimp shells during bacterial deproteination and demineralization

BACKGROUND: After cellulose and starch, chitin is the third-most abundant biopolymer on earth. Chitin or its deacetylated derivative chitosan is a valuable product with a number of applications. It is one of the main components of shrimp shells, a waste product of the fish industry. To obtain chitin...

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Autores principales: Xu, Youmei, Bajaj, Mini, Schneider, Reinhard, Grage, Stephan L, Ulrich, Anne S, Winter, Josef, Gallert, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3852495/
https://www.ncbi.nlm.nih.gov/pubmed/24093594
http://dx.doi.org/10.1186/1475-2859-12-90
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author Xu, Youmei
Bajaj, Mini
Schneider, Reinhard
Grage, Stephan L
Ulrich, Anne S
Winter, Josef
Gallert, Claudia
author_facet Xu, Youmei
Bajaj, Mini
Schneider, Reinhard
Grage, Stephan L
Ulrich, Anne S
Winter, Josef
Gallert, Claudia
author_sort Xu, Youmei
collection PubMed
description BACKGROUND: After cellulose and starch, chitin is the third-most abundant biopolymer on earth. Chitin or its deacetylated derivative chitosan is a valuable product with a number of applications. It is one of the main components of shrimp shells, a waste product of the fish industry. To obtain chitin from Penaeus monodon, wet and dried shrimp shells were deproteinated with two specifically enriched proteolytic cultures M1 and M2 and decalcified by in-situ lactic acid forming microorganisms. The viscosity of biologically processed chitin was compared with chemically processed chitin. The former was further investigated for purity, structure and elemental composition by several microscopic techniques and (13)C solid state NMR spectroscopy. RESULTS: About 95% of the protein of wet shrimp shells was removed by proteolytic enrichment culture M2 in 68 h. Subsequent decalcification by lactic acid bacteria (LAB) took 48 h. Deproteination of the same amount of dried shrimps that contained a 3 × higher solid content by the same culture was a little bit faster and was finished after 140 h. The viscosity of chitin was in the order of chemically processed chitin > bioprocessed chitin > commercially available chitin. Results revealed changes in fine structure and chemical composition of the epi-, exo- and endocuticle of chitin from shrimp shells during microbial deproteination and demineralization. From transmission electron microscopy (TEM) overlays and electron energy loss spectroscopy (EELS) analysis, it was found that most protein was present in the exocuticle, whereas most chitin was present in the endocuticle. The calcium content was higher in the endocuticle than in the exocuticle.(13)C solid state NMR spectra of different chitin confirmed < 3% impurities in the final product. CONCLUSIONS: Bioprocessing of shrimp shell waste resulted in a chitin with high purity. Its viscosity was higher than that of commercially available chitin but lower than that of chemically prepared chitin in our lab. Nevertheless, the biologically processed chitin is a promising alternative for less viscous commercially available chitin. Highly viscous chitin could be generated by our chemical method. Comprehensive structural analyses revealed the distribution of the protein and Ca matrix within the shrimp shell cuticle which might be helpful in developing shrimp waste processing techniques.
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spelling pubmed-38524952013-12-06 Transformation of the matrix structure of shrimp shells during bacterial deproteination and demineralization Xu, Youmei Bajaj, Mini Schneider, Reinhard Grage, Stephan L Ulrich, Anne S Winter, Josef Gallert, Claudia Microb Cell Fact Research BACKGROUND: After cellulose and starch, chitin is the third-most abundant biopolymer on earth. Chitin or its deacetylated derivative chitosan is a valuable product with a number of applications. It is one of the main components of shrimp shells, a waste product of the fish industry. To obtain chitin from Penaeus monodon, wet and dried shrimp shells were deproteinated with two specifically enriched proteolytic cultures M1 and M2 and decalcified by in-situ lactic acid forming microorganisms. The viscosity of biologically processed chitin was compared with chemically processed chitin. The former was further investigated for purity, structure and elemental composition by several microscopic techniques and (13)C solid state NMR spectroscopy. RESULTS: About 95% of the protein of wet shrimp shells was removed by proteolytic enrichment culture M2 in 68 h. Subsequent decalcification by lactic acid bacteria (LAB) took 48 h. Deproteination of the same amount of dried shrimps that contained a 3 × higher solid content by the same culture was a little bit faster and was finished after 140 h. The viscosity of chitin was in the order of chemically processed chitin > bioprocessed chitin > commercially available chitin. Results revealed changes in fine structure and chemical composition of the epi-, exo- and endocuticle of chitin from shrimp shells during microbial deproteination and demineralization. From transmission electron microscopy (TEM) overlays and electron energy loss spectroscopy (EELS) analysis, it was found that most protein was present in the exocuticle, whereas most chitin was present in the endocuticle. The calcium content was higher in the endocuticle than in the exocuticle.(13)C solid state NMR spectra of different chitin confirmed < 3% impurities in the final product. CONCLUSIONS: Bioprocessing of shrimp shell waste resulted in a chitin with high purity. Its viscosity was higher than that of commercially available chitin but lower than that of chemically prepared chitin in our lab. Nevertheless, the biologically processed chitin is a promising alternative for less viscous commercially available chitin. Highly viscous chitin could be generated by our chemical method. Comprehensive structural analyses revealed the distribution of the protein and Ca matrix within the shrimp shell cuticle which might be helpful in developing shrimp waste processing techniques. BioMed Central 2013-10-05 /pmc/articles/PMC3852495/ /pubmed/24093594 http://dx.doi.org/10.1186/1475-2859-12-90 Text en Copyright © 2013 Xu et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Xu, Youmei
Bajaj, Mini
Schneider, Reinhard
Grage, Stephan L
Ulrich, Anne S
Winter, Josef
Gallert, Claudia
Transformation of the matrix structure of shrimp shells during bacterial deproteination and demineralization
title Transformation of the matrix structure of shrimp shells during bacterial deproteination and demineralization
title_full Transformation of the matrix structure of shrimp shells during bacterial deproteination and demineralization
title_fullStr Transformation of the matrix structure of shrimp shells during bacterial deproteination and demineralization
title_full_unstemmed Transformation of the matrix structure of shrimp shells during bacterial deproteination and demineralization
title_short Transformation of the matrix structure of shrimp shells during bacterial deproteination and demineralization
title_sort transformation of the matrix structure of shrimp shells during bacterial deproteination and demineralization
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3852495/
https://www.ncbi.nlm.nih.gov/pubmed/24093594
http://dx.doi.org/10.1186/1475-2859-12-90
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