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Enzymatic Modification of Native Chitin and Conversion to Specialty Chemical Products

Chitin is one of the most abundant biomolecules on earth, occurring in crustacean shells and cell walls of fungi. While the polysaccharide is threatening to pollute coastal ecosystems in the form of accumulating shell-waste, it has the potential to be converted into highly profitable derivatives wit...

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Autores principales: Arnold, Nathanael D., Brück, Wolfram M., Garbe, Daniel, Brück, Thomas B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7073968/
https://www.ncbi.nlm.nih.gov/pubmed/32019265
http://dx.doi.org/10.3390/md18020093
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author Arnold, Nathanael D.
Brück, Wolfram M.
Garbe, Daniel
Brück, Thomas B.
author_facet Arnold, Nathanael D.
Brück, Wolfram M.
Garbe, Daniel
Brück, Thomas B.
author_sort Arnold, Nathanael D.
collection PubMed
description Chitin is one of the most abundant biomolecules on earth, occurring in crustacean shells and cell walls of fungi. While the polysaccharide is threatening to pollute coastal ecosystems in the form of accumulating shell-waste, it has the potential to be converted into highly profitable derivatives with applications in medicine, biotechnology, and wastewater treatment, among others. Traditionally this is still mostly done by the employment of aggressive chemicals, yielding low quality while producing toxic by-products. In the last decades, the enzymatic conversion of chitin has been on the rise, albeit still not on the same level of cost-effectiveness compared to the traditional methods due to its multi-step character. Another severe drawback of the biotechnological approach is the highly ordered structure of chitin, which renders it nigh impossible for most glycosidic hydrolases to act upon. So far, only the Auxiliary Activity 10 family (AA10), including lytic polysaccharide monooxygenases (LPMOs), is known to hydrolyse native recalcitrant chitin, which spares the expensive first step of chemical or mechanical pre-treatment to enlarge the substrate surface. The main advantages of enzymatic conversion of chitin over conventional chemical methods are the biocompability and, more strikingly, the higher product specificity, product quality, and yield of the process. Products with a higher M(w) due to no unspecific depolymerisation besides an exactly defined degree and pattern of acetylation can be yielded. This provides a new toolset of thousands of new chitin and chitosan derivatives, as the physio-chemical properties can be modified according to the desired application. This review aims to provide an overview of the biotechnological tools currently at hand, as well as challenges and crucial steps to achieve the long-term goal of enzymatic conversion of native chitin into specialty chemical products.
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spelling pubmed-70739682020-03-19 Enzymatic Modification of Native Chitin and Conversion to Specialty Chemical Products Arnold, Nathanael D. Brück, Wolfram M. Garbe, Daniel Brück, Thomas B. Mar Drugs Review Chitin is one of the most abundant biomolecules on earth, occurring in crustacean shells and cell walls of fungi. While the polysaccharide is threatening to pollute coastal ecosystems in the form of accumulating shell-waste, it has the potential to be converted into highly profitable derivatives with applications in medicine, biotechnology, and wastewater treatment, among others. Traditionally this is still mostly done by the employment of aggressive chemicals, yielding low quality while producing toxic by-products. In the last decades, the enzymatic conversion of chitin has been on the rise, albeit still not on the same level of cost-effectiveness compared to the traditional methods due to its multi-step character. Another severe drawback of the biotechnological approach is the highly ordered structure of chitin, which renders it nigh impossible for most glycosidic hydrolases to act upon. So far, only the Auxiliary Activity 10 family (AA10), including lytic polysaccharide monooxygenases (LPMOs), is known to hydrolyse native recalcitrant chitin, which spares the expensive first step of chemical or mechanical pre-treatment to enlarge the substrate surface. The main advantages of enzymatic conversion of chitin over conventional chemical methods are the biocompability and, more strikingly, the higher product specificity, product quality, and yield of the process. Products with a higher M(w) due to no unspecific depolymerisation besides an exactly defined degree and pattern of acetylation can be yielded. This provides a new toolset of thousands of new chitin and chitosan derivatives, as the physio-chemical properties can be modified according to the desired application. This review aims to provide an overview of the biotechnological tools currently at hand, as well as challenges and crucial steps to achieve the long-term goal of enzymatic conversion of native chitin into specialty chemical products. MDPI 2020-01-30 /pmc/articles/PMC7073968/ /pubmed/32019265 http://dx.doi.org/10.3390/md18020093 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Arnold, Nathanael D.
Brück, Wolfram M.
Garbe, Daniel
Brück, Thomas B.
Enzymatic Modification of Native Chitin and Conversion to Specialty Chemical Products
title Enzymatic Modification of Native Chitin and Conversion to Specialty Chemical Products
title_full Enzymatic Modification of Native Chitin and Conversion to Specialty Chemical Products
title_fullStr Enzymatic Modification of Native Chitin and Conversion to Specialty Chemical Products
title_full_unstemmed Enzymatic Modification of Native Chitin and Conversion to Specialty Chemical Products
title_short Enzymatic Modification of Native Chitin and Conversion to Specialty Chemical Products
title_sort enzymatic modification of native chitin and conversion to specialty chemical products
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7073968/
https://www.ncbi.nlm.nih.gov/pubmed/32019265
http://dx.doi.org/10.3390/md18020093
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