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Expression and Characterization of an Alginate Lyase and Its Thermostable Mutant inPichia pastoris

文献类型： 外文期刊

作者： Yang, Suxiao 1 ; Liu, Zhemin 1 ; Fu, Xiaodan 1 ; Zhu, Changliang 1 ; Kong, Qing 1 ; Yang, Min 2 ; Mou, Haijin 1 ;

作者机构： 1.Ocean Univ China, Coll Food Sci & Engn, Qingdao 266003, Peoples R China

2.Chinese Acad Fishery Sci, Yellow Sea Fisheries Res Inst, Lab Marine Drugs & Bioprod, Pilot Natl Lab Marine Sci & Technol, Qingdao 266071, Peoples R China

关键词： Pichia pastoris; alginate lyase; thermostable mutant; alginate oligosaccharides

期刊名称：MARINE DRUGS （ 影响因子：5.118； 五年影响因子：5.951 ）

ISSN：

年卷期： 2020 年 18 卷 6 期

页码：

收录情况： SCI

摘要： Alginate is one of the most abundant polysaccharides in algae. Alginate lyase degrades alginate through a beta-elimination mechanism to produce alginate oligosaccharides with special bioactivities. Improving enzyme activity and thermal stability can promote the application of alginate lyase in the industrial preparation of alginate oligosaccharides. In this study, the recombinant alginate lyase cAlyM and its thermostable mutant 102C300C were expressed and characterized inPichia pastoris. The specific activities of cAlyM and 102C300C were 277.1 U/mg and 249.6 U/mg, respectively. Both enzymes showed maximal activity at 50 degrees C and pH 8.0 and polyG preference. The half-life values of 102C300C at 45 degrees C and 50 degrees C were 2.6 times and 11.7 times the values of cAlyM, respectively. The degradation products of 102C300C with a lower degree of polymerization contained more guluronate. The oligosaccharides with a polymerization degree of 2-4 were the final hydrolytic products. Therefore, 102C300C is potentially valuable in the production of alginate oligosaccharides with specific M/G ratio and molecular weights.

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