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首页> 外文期刊>Marine biotechnology >Surface Display of GFP by Pseudomonas Syringae Truncated Ice Nucleation Protein in Attenuated Vibrio Anguillarum Strain
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Surface Display of GFP by Pseudomonas Syringae Truncated Ice Nucleation Protein in Attenuated Vibrio Anguillarum Strain

机译:丁香假单胞菌截短的冰核蛋白在减毒弧菌菌株中GFP的表面展示。

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摘要

Microbial cell surface display of foreign proteins has been widely developed for many potential applications in live vaccine construction, whole-cell biocatalysts, and bioadsorption. To investigate the feasibility of displaying heterologous proteins on the surface of attenuated Vibrio anguillarum strain for potential multivalent live vaccine development, different display systems were built upon a truncated ice nucleation protein (INP) from Pseudomonas syringae ICMP3023 whose N- and C-terminal domains were considered to be the putative membrane-anchoring motifs. Green fluorescent protein (GFP), as a reporter, was fused with the display systems in different forms of N-GFP, NC-GFP, and N-GFP-C. Analysis of the total expression level and surface localization of GFP demonstrated that the truncated P. syringae INP could be used to display foreign protein in V. anguillarum, while the system of N-GFP showed the higher levels of total expression and surface display based on unit cell density among the three and might be available for further carrier vaccine development.
机译:对于活疫苗构建,全细胞生物催化剂和生物吸附中的许多潜在应用,已经广泛开发了外源蛋白质在微生物细胞表面的展示。为了研究在减毒鳗弧菌菌株表面上展示异源蛋白用于潜在多价活疫苗开发的可行性,在丁香假单胞菌ICMP3023的截短的冰核蛋白(INP)上构建了不同的展示系统,该蛋白的N和C端结构域为被认为是假定的膜锚定基元。作为报告基因,绿色荧光蛋白(GFP)以不同形式的N-GFP,NC-GFP和N-GFP-C与展示系统融合。对GFP的总表达水平和表面定位的分析表明,截短的丁香假单胞菌INP可用于显示鳗弧菌中的外源蛋白,而N-GFP系统显示较高的总表达水平和表面展示。这三者之间的单位细胞密度可能会用于进一步的载体疫苗开发。

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