Cloning and Expression of Marine α-Glucosidase and Its Preparation of High Purity Panose

被引:0
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作者
Yu, Yiqun [1 ,2 ]
Xue, Luzhou [1 ,2 ]
Ni, Hao [1 ,2 ]
Jiang, Lei [1 ,2 ]
Kang, Xinxin [1 ,2 ]
Pan, Saikun [1 ,2 ]
Wang, Shujun [1 ,2 ]
机构
[1] Key Laboratory of Marine Biological Resources and Environment of Jiangsu Province, Jiangsu Ocean University, Lianyungang,222005, China
[2] Key Laboratory of Marine Biotechnology of Jiangsu Province, Jiangsu Ocean University, Lianyungang,222005, China
关键词
Clone cells - Escherichia coli - Fructose;
D O I
10.13386/j.issn1002-0306.2023110185
中图分类号
学科分类号
摘要
Panose is iso-malto-oligosaccharide contained α-1,6 glycosidic bonds, and α-glucosidase is the key enzyme to produce panose. In this study, the α-glucosidase gene in deep-sea hydrothermal vents thermophilic archaea Thermococcus siculi HJ21 was synthesized, and cloned into the vector pET29a. Then expressed in Escherichia coli BL21 and purified by His Trap HP column. The molecular weight of α-glucosidase was determined by SDS-PAGE. The enzymatic properties and transglycosylation were also investigated. The results showed that the gene of α-glucosidase was 729 bp and encoded 242 amino acids. The molecular weight of α-glucosidase was about 27.2 kDa. Its optimal temperature and pH were 40 ℃ and 6.0 respectively. When the receptor was fructose, and the ratio of fructose and maltose was 1:9, the highest yield of panose could reached 79.1% after 10 h reaction. The results provide a basis for producing high-purity panose by α-glucosidase from archaea. © 2024 Editorial Department of Science and Technology of Food Science. All rights reserved.
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页码:158 / 165
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