Characterization of extracellular chitinase from Chitinibacter sp GC72 and its application in GlcNAc production from crayfish shell enzymatic degradation

被引:54
作者
Gao, Cong [1 ,2 ]
Zhang, Alei [1 ]
Chen, Kequan [1 ]
Hao, Zhikui [3 ]
Tong, Junmao [2 ]
Ouyang, Pingkai [1 ]
机构
[1] Nanjing Univ Technol, Coll Biotechnol & Pharmaceut Engn, Nanjing 211816, Jiangsu, Peoples R China
[2] Shihezi Univ, Food Coll, Shihezi City 832003, Peoples R China
[3] Taizhou Vocat & Tech Coll, Taizhou City 318000, Peoples R China
关键词
Chitinase; Chitinibacter; Purification; Biodegradation; Waste treatment; Enzyme biocatalysis; ACETYL-D-GLUCOSAMINE; N-ACETYLGLUCOSAMINE; HETEROLOGOUS EXPRESSION; CHITINOLYTIC BACTERIUM; BACILLUS-LICHENIFORMIS; ALPHA-CHITIN; PURIFICATION; ACID; TEMPERATURE; EXTRACTION;
D O I
10.1016/j.bej.2015.02.010
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
In this study, a novel chitinase-producing bacterium Chitinibacter sp. GC72 was isolated and investigated for N-acetyl-D-glucosamine production from crayfish shell enzymatic degradation. A dimeric chitinase was purified, which had an optimal activity at a pH of 6.8 and 40 degrees C. The metal ions Al3+, Cu2+, and Zn2+ inhibited the chitinase activity, whereas Ca2+, Mn2+, and Mg2+ promoted the activity. The chitinase was active on p-NP-GlcNAc with apparent K-m value of 152.83 mu mol/L and V-m value of 49.12 mu mol/L min at 37 degrees C. Based on the hydrolysate formed, the chitinase was characterized as an exo-hydrolytic N-acetyl glucosaminidase. Furthermore, combined treatment of ultra-micro grinding and ultrasonic with direct enzymatic hydrolysis of crayfish shell for GlcNAc production was investigated, which resulted in 15.2 g of GlcNAc production from 100g of crayfish shell following chitinase degradation for 36 h. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:59 / 64
页数:6
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