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利用优化的几丁质酶混合物从脱脂磷虾副产物中生产 N,N'-二乙酰壳二糖和 N-乙酰-d-葡萄糖胺。

An optimized cocktail of chitinolytic enzymes to produce N,N'-diacetylchitobiose and N-acetyl-d-glucosamine from defatted krill by-products.

机构信息

State Key Laboratory of Fine Chemical Engineering and School of Life Science and Biotechnology, Dalian University of Technology, Dalian 116024, China.

State Key Laboratory of Fine Chemical Engineering and School of Life Science and Biotechnology, Dalian University of Technology, Dalian 116024, China.

出版信息

Int J Biol Macromol. 2019 Jul 15;133:1029-1034. doi: 10.1016/j.ijbiomac.2019.04.114. Epub 2019 Apr 17.

DOI:10.1016/j.ijbiomac.2019.04.114
PMID:31004644
Abstract

Defatted krill powder (DKP), the byproduct of krill oil industry, is a resource of biological macromolecules. Here, one bacterial protease, three bacterial chitinases and one insect N-acetyl-d-hexosaminidase were integratively used to produce peptide, N,N'-diacetylchitobiose [(GlcNAc)] and N-acetyl-d-glucosamine (GlcNAc) from DKP. First, alkaline protease was found to outperform neutral protease in deproteinizing DKP and the resultant krill peptides were rich in essential amino acids (41.4%). Second, the mutant of chitinase A from Serratia marcescens [SmChiA-F232W/F396W (SmChiA-M)] was found to be 32% faster than wild-type SmChiA in hydrolyzing the deproteinized DKP (DDKP) and showed significant synergy with chitinase B from S. marcescens (SmChiB) and chitinase C from S. marcescens (SmChiC). Then two SmChiA-M-based enzyme combinations [SmChiA-M + SmChiB + SmChiC and SmChiA-M + SmChiB + SmChiC + OfHex1 (an insect N-acetyl-d-hexosaminidase from Ostrinia furnacalis)] were designed to produce (GlcNAc) and GlcNAc, respectively, from DDKP. A yield of 2.04 g/L (GlcNAc) or 2.71 g/L GlcNAc (each with 95% purity) could be obtained from 20 g/L DDKP in 24 h.

摘要

脱脂磷虾粉(DKP)是磷虾油工业的副产品,是生物大分子的资源。在这里,一种细菌蛋白酶、三种细菌几丁质酶和一种昆虫 N-乙酰-d-氨基葡萄糖苷酶被综合用于从 DKP 生产肽、N,N'-二乙酰壳二糖 [(GlcNAc)] 和 N-乙酰-d-葡萄糖胺(GlcNAc)。首先,碱性蛋白酶在脱蛋白 DKP 方面表现优于中性蛋白酶,所得磷虾肽富含必需氨基酸(41.4%)。其次,发现沙雷氏菌来源的几丁质酶 A 的突变体[SmChiA-F232W/F396W(SmChiA-M)]在水解脱蛋白的 DKP(DDKP)方面比野生型 SmChiA 快 32%,并与沙雷氏菌来源的几丁质酶 B(SmChiB)和沙雷氏菌来源的几丁质酶 C(SmChiC)表现出显著协同作用。然后设计了两种基于 SmChiA-M 的酶组合[SmChiA-M+SmChiB+SmChiC 和 SmChiA-M+SmChiB+SmChiC+OfHex1(一种来自东方粘虫的昆虫 N-乙酰-d-氨基葡萄糖苷酶)],分别从 DDKP 生产(GlcNAc)和 GlcNAc。在 24 小时内,可以从 20 g/L 的 DDKP 中获得 2.04 g/L(GlcNAc)或 2.71 g/L GlcNAc(每种纯度均为 95%)。

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