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首页|期刊导航|食品科学|嗜热链球菌LMG 18311来源右旋糖酐酶的生物信息学分析、异源表达及酶学性质表征

嗜热链球菌LMG 18311来源右旋糖酐酶的生物信息学分析、异源表达及酶学性质表征

魏真 陈金玲 徐淋香

食品科学2025,Vol.46Issue(22):246-256,11.
食品科学2025,Vol.46Issue(22):246-256,11.DOI:10.7506/spkx1002-6630-20250617-118

嗜热链球菌LMG 18311来源右旋糖酐酶的生物信息学分析、异源表达及酶学性质表征

Bioinformatics Analysis,Heterologous Expression and Enzymatic Characterization of Dextranase from Streptococcus thermophiles LMG 18311

魏真 1陈金玲 2徐淋香1

作者信息

  • 1. 江苏海洋大学江苏省海洋生物资源与环境重点实验室,江苏 连云港 222005||江苏省海洋生物产业技术协同创新中心,江苏 连云港 222005||江苏省海洋资源开发研究院(连云港),江苏 连云港 222005
  • 2. 江苏海洋大学江苏省海洋生物资源与环境重点实验室,江苏 连云港 222005||江苏省海洋生物产业技术协同创新中心,江苏 连云港 222005
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摘要

Abstract

In this study,bioinformatics analysis,heterologous expression and enzymatic characterization of dextranase(StDex)from Streptococcus thermophilus LMG 18311 were conducted to expand the dextranase resource library and lay the foundation for further research on its thermostability mechanism and its application in functional foods.The bioinformatics analysis indicated that StDex contained 166 amino acids with a theoretical molecular mass of 18.60 kDa and an isoelectric point of 6.59.It was a stable hydrophilic protein with a stable low molecular mass.StDex belonged to the glycoside hydrolase(GH)66 family.Homology modeling showed that its catalytic site characteristics were significantly different from those of other dextranases,indicating that this enzyme might have a unique hydrolysis mechanism.Heterologous soluble expression of StDex was achieved using the pET28a-SUMO vector.After purification by Ni-chelating affinity chromatography,the specific activity of the recombinant StDex reached 90.18 U/mg.The enzymatic characterization indicated that the optimal catalytic conditions for the recombinant StDex were 50℃and pH 7.0.This enzyme retained more than 60%of its original activity after 1 h of incubation at 20-65℃,and retained more than 80%of its original activity after 1 h of incubation at pH 4.0-8.0.Dextran T20 was found to be the most suitable substrate for the enzyme,and its relative activities towards dextran T10,T40 and T70 all exceeded 70.36%;its relative activity towards soluble starch was 46.74%.Ca2+,Ba2+,and Fe3+at concentrations of 1-5 mmol/L had no significant inhibitory effect on the activity of StDex.More than 88%of its activity remained after treatment with 10 mmol/L Ca2+,Fe3+,Ni2+or Mn2+,and the addition of 0.1%sodium fluoride increased its activity by 14.53%.Compared with dextran T10,T20,T40 and T70,StDex had the smallest Km value of 5.40 μmol/L and the largest kcat/Km value of 90.44 L/(μmol·min)for dextran T500,indicating that it had a higher substrate affinity and catalytic efficiency for dextran with a higher molecular mass.The major products produced from the hydrolysis of dextran T20 and T500 by StDex were both isomaltooligosaccharides ranging from triose to heptaose,and their oligosaccharide products all exhibited high antioxidant activity.The results of this study provide a theoretical basis for the application of StDex in the prevention and treatment of dental caries,the preparation of active oligosaccharides,and the development of functional foods.

关键词

嗜热链球菌/右旋糖酐酶/异源表达/酶学性质

Key words

Streptococcus thermophilus/dextranase/heterologous expression/enzymatic properties

分类

轻工业

引用本文复制引用

魏真,陈金玲,徐淋香..嗜热链球菌LMG 18311来源右旋糖酐酶的生物信息学分析、异源表达及酶学性质表征[J].食品科学,2025,46(22):246-256,11.

基金项目

江苏海洋大学科研启动基金项目(KQ19052) (KQ19052)

连云港市第六期"521高层次人才培养工程"科研项目(LYG06521202396) (LYG06521202396)

江苏省高校自然科学基金面上项目(22KJB180015) (22KJB180015)

食品科学

OA北大核心

1002-6630

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