TY - JOUR
T1 - Enzymatic hydrolysis of chitinous wastes pretreated by deep eutectic solvents into N-acetyl glucosamine
AU - Zhou, Xi
AU - Liu, Quanzhen
AU - Chen, Xueman
AU - Zhou, Ning
AU - Wei, Guoguang
AU - Chen, Feifei
AU - Zhang, Alei
AU - Chen, Kequan
N1 - Publisher Copyright:
© 2024 Elsevier Ltd
PY - 2024/9
Y1 - 2024/9
N2 - In this study, we present an efficient and green extraction-pretreatment integrated approach for enhancing enzymatic conversion of chitinous wastes into N-acetyl-d-glucosamine (GlcNAc). Firstly, the enzyme cocktail containing a chitinase CmChi1 and a N-acetyl glucosaminase CmNAGase were constructed for hydrolyzing chitin into sole GlcNAc. Secondly, deep eutectic solvent (DES), consisting of choline chloride and glycollic acid was used to treat chitinous wastes. Under optimal conditions, chitin yield reach to 72 % with a purity of 98 %. Fourier-transform infrared spectroscopy, thermogravimetric analysis, and X-ray diffraction analysis revealed that the crystallinity and thermal stability of the obtained chitin decreased upon DES treatment without alteration of the chemical structure or deacetylation. Finally, the concentration of GlcNAc was increased 2–6 folds by enzymatic hydrolysis of DES-treated chitinous wastes (including shrimp shell, crab shell, ganoderma spores wall, and mycelium). The process provides a promising strategy for degrading chitinous wastes to produce high valued GlcNAc.
AB - In this study, we present an efficient and green extraction-pretreatment integrated approach for enhancing enzymatic conversion of chitinous wastes into N-acetyl-d-glucosamine (GlcNAc). Firstly, the enzyme cocktail containing a chitinase CmChi1 and a N-acetyl glucosaminase CmNAGase were constructed for hydrolyzing chitin into sole GlcNAc. Secondly, deep eutectic solvent (DES), consisting of choline chloride and glycollic acid was used to treat chitinous wastes. Under optimal conditions, chitin yield reach to 72 % with a purity of 98 %. Fourier-transform infrared spectroscopy, thermogravimetric analysis, and X-ray diffraction analysis revealed that the crystallinity and thermal stability of the obtained chitin decreased upon DES treatment without alteration of the chemical structure or deacetylation. Finally, the concentration of GlcNAc was increased 2–6 folds by enzymatic hydrolysis of DES-treated chitinous wastes (including shrimp shell, crab shell, ganoderma spores wall, and mycelium). The process provides a promising strategy for degrading chitinous wastes to produce high valued GlcNAc.
KW - Chitinolytic enzymes
KW - Chitinous wastes
KW - Deep eutectic solvents
KW - N-acetyl glucosamine
UR - http://www.scopus.com/inward/record.url?scp=85197078899&partnerID=8YFLogxK
U2 - 10.1016/j.polymdegradstab.2024.110907
DO - 10.1016/j.polymdegradstab.2024.110907
M3 - 文章
AN - SCOPUS:85197078899
SN - 0141-3910
VL - 227
JO - Polymer Degradation and Stability
JF - Polymer Degradation and Stability
M1 - 110907
ER -