| 注册
首页|期刊导航|生物加工过程|贻贝足蛋白fp-5在大肠杆菌中的表达、修饰与功能分析

贻贝足蛋白fp-5在大肠杆菌中的表达、修饰与功能分析

姚林 谢紫莎 王瑞 张鲁嘉 李莎

生物加工过程2024,Vol.22Issue(1):25-32,8.
生物加工过程2024,Vol.22Issue(1):25-32,8.DOI:10.3969/j.issn.1672-3678.2024.01.004

贻贝足蛋白fp-5在大肠杆菌中的表达、修饰与功能分析

Expression,modification and functional analysis of mussel foot protein fp-5 in Escherichia coli

姚林 1谢紫莎 1王瑞 2张鲁嘉 3李莎2

作者信息

  • 1. 南京工业大学食品与轻工学院,江苏 南京 211800
  • 2. 南京工业大学食品与轻工学院,江苏 南京 211800||南京工业大学材料化学工程国家重点实验室,江苏 南京 211800
  • 3. 华东师范大学 化学与分子工程学院,上海 201100
  • 折叠

摘要

Abstract

The co-expression of Mytilus galloprovincialis foot protein fp-5 and tyrosinase from different bacterial sources in E.coli could produce the modified mussel foot protein with improved in vivo performance.Through sequence analysis and codon optimization,both single-vector and dual-vector co-expression systems were constructed with tyrosinase and mussel foot protein genes,and the subsequent expression proved to be successful in E.coli.The purified protein was analyzed by NBT/Gly staining test and acid-borate differential spectroscopy,showing a wide range of hydroxylation levels in the resultant fp-5.The co-expression of fp-5 and tyrosinase derived from Verrucomicrobium spinosum(TyrVs)reached a concentration of 18.6 mg/L,along with 55.2%modification rate.Moreover,the 5-Vs from such co-expression showed much higher adhesion force(4.6 times)than the unmodified fp-5.Due to the excellent adsorption and adhesion,the 5-Vs modified in vivo by TyrVs will provide a potential bio-glue material for biomedicine and other fields.

关键词

贻贝足蛋白/酪氨酸酶/共表达/大肠杆菌/体内修饰

Key words

mussel foot protein/tyrosinase/co-expression/Escherichia coli/modification in vivo

分类

生物科学

引用本文复制引用

姚林,谢紫莎,王瑞,张鲁嘉,李莎..贻贝足蛋白fp-5在大肠杆菌中的表达、修饰与功能分析[J].生物加工过程,2024,22(1):25-32,8.

基金项目

国家重点研发计划(2019YFA0905203) (2019YFA0905203)

国家自然科学基金(22178177) (22178177)

江苏省先进生物制造创新中心项目自主课题(XTD2201) (XTD2201)

生物加工过程

OACSTPCD

1672-3678

访问量0
|
下载量0
段落导航相关论文