研究报告

植物乳杆菌植酸酶理性设计及表达鉴定

  • 唐存多 ,
  • 杨田田 ,
  • 李莹 ,
  • 王喆 ,
  • 何建菊 ,
  • 杨露露 ,
  • 史红玲
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  • 1(南阳师范学院 河南省伏牛山昆虫生物学重点实验室,河南 南阳,473061)
    2(南阳师范学院 生命科学与农业工程学院,河南 南阳,473061)
博士,副教授(史红玲实验师为通信作者,E-mail:shihonglingwu2006@163.com)

收稿日期: 2022-05-19

  修回日期: 2022-06-10

  网络出版日期: 2023-04-28

基金资助

国家自然科学基金项目(31900916);河南省青年人才托举工程项目(2021HYTP036);南阳师范学院青年项目(2020QN003);河南省高校科技创新人才(21HASTIT041)和河南省本科高校省级大学生创新创业训练计划项目(S202110481033)

Rational design and expression identification of phytase from Lactobacillus plantarum

  • TANG Cunduo ,
  • YANG Tiantian ,
  • LI Ying ,
  • WANG Zhe ,
  • HE Jianju ,
  • YANG Lulu ,
  • SHI Hongling
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  • 1(Henan Provincial Key laboratory of Funiu Mountain Insect Biology, Nanyang Normal University, Nanyang 473061, China)
    2 (School of Life Sciences and Agricultural Engineering, Nanyang Normal University, Nanyang 473061, China)

Received date: 2022-05-19

  Revised date: 2022-06-10

  Online published: 2023-04-28

摘要

植酸酶能将植酸水解成肌醇衍生物,并释放出无机磷酸,是一种重要的生物催化剂。植酸酶的热稳定性和比活性是决定其潜在应用价值的2个关键因素。该研究从植物乳杆菌中克隆到了具有233个氨基酸残基、高活性的植酸酶基因(LpPHY233),并在大肠杆菌中实现了高水平的异源表达,其表达水平是植物乳杆菌的800倍。基于理性设计的结果,通过二硫键工程显著提高了LpPHY233的温度特性和催化性能。突变体LpPHY233S58C/K61C的最适反应温度较LpPHY233提高了15 ℃。此外,它还具有良好的pH特性和动力学参数,在食品加工和饲料添加剂领域具有较大的应用前景。该研究结果为植酸酶的进一步分子修饰和工业应用提供了坚实的理论基础。

本文引用格式

唐存多 , 杨田田 , 李莹 , 王喆 , 何建菊 , 杨露露 , 史红玲 . 植物乳杆菌植酸酶理性设计及表达鉴定[J]. 食品与发酵工业, 2023 , 49(7) : 9 -15 . DOI: 10.13995/j.cnki.11-1802/ts.032372

Abstract

Phytase is an important biocatalyst that can dissociate phytate into inositol derivatives and release inorganic phosphoric acid. It can be used as feed additive to reduce phytate anti-nutrient factor in feed. The thermal stability and specific activity of phytase are two key factors that determine its application potential. In this study, a phytase gene with 233 amino acid residues (LpPHY233) was cloned from Lactobacillus plantarum, and the highly heterologous expression was achieved in Escherichia coli, which was 800 times higher than that of L. plantarum. Then, based on the results of in silico design, the temperature characteristics and catalytic performance of LpPHY233 were significantly improved by disulfide bond engineering. The optimal reaction temperature of LpPHY233S58C/K61C was 15 ℃ higher than that of LpPHY233. In addition, it also has good pH characteristics and kinetic parameters, which has a broad application potential in the feed additives field. This study provides a solid theoretical basis for further molecular modification and industrial application of phytases.

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