Journal
BIOCHEMICAL ENGINEERING JOURNAL
Volume 97, Issue -, Pages 59-64Publisher
ELSEVIER
DOI: 10.1016/j.bej.2015.02.010
Keywords
Chitinase; Chitinibacter; Purification; Biodegradation; Waste treatment; Enzyme biocatalysis
Funding
- National Nature Science Foundation of China [21390200, 21106068]
- National Key Technology Support Program [2012BAI44G00]
- 973 Program of China [2011CBA00807]
- 863 Program of China [2014AA021703]
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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.
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