
Document généré le 16/09/2025 depuis l'adresse: https://www.documentation.eauetbiodiversite.fr/fr/notice/purification-de-la-chitine-par-hydrolyse-enzymatique-a-partir-de-coproduits-de-crevette-penaeus-vannamei-caracterisations-des-produits-et-optimisation-du-procede
Purification de la chitine par hydrolyse enzymatique à partir de coproduits de crevette Penaeus vannamei. Caractérisations des produits et optimisation du procédé
Titre alternatif
Producteur
Contributeur(s)
Université de Nantes
Identifiant documentaire
9-19828
Identifiant OAI
oai:archimer.ifremer.fr:19828
Auteur(s):
Le Roux, Karine
Mots clés
coproduits de crustacés
hydrolyse enzymatique
protéolyse
chitine
extraction
cinétique
déminéralisation
déprotéinisation
crustacean by-products
enzymatic hydrolysis
proteolysis
chitin
extraction
kinetic
demineralization
deproteinization
Date de publication
04/05/2012
Date de création
Date de modification
Date d'acceptation du document
Date de dépôt légal
Langue
fre
Thème
Type de ressource
Source
Droits de réutilisation
2012 the author, Univ. Nantes
Région
Département
Commune
Description
The objective of this study was to optimize the extraction of chitin by acid proteolysis. The novelty of the method is based on the stabilization of pH by the balance between substrate composition and the acid solvent. This principle allows a simultaneous demineralization and deproteinization, the two main reactions associated with the purification of chitin. To evaluate the performance of this purification, the composition of the substrate and products was characterized. Different methods of quantification of chitin and proteins have been compared. As traditional assays were not satisfaying, a direct method of amino acids determination by gaz chromatography was selected to estimate the amount of protein. The estimate of chitin amount was based on indirect methods, mainly gravimetry, elemental analysis and thermogravimetric analysis (TGA). Kinetics of demineralization and deproteinization were examined to optimize the purification of chitin. Mass balances confirmed the consistency of results. The quality of chitin extracted by enzymatic or chemical techniques was compared with the degree of acetylation and depolymerization and the crystallinity index of chitin. The structure of chitin was also observed by scanning electron microscopy (SEM). Finally, compounds solubilized by enzymatic hydrolysis were identified and quantified.
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