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Surface display of GFP by Pseudomonas syringae truncated ice nucleation protein in attenuated Vibrio anguillarum strain
Xu, Y.; Liu, Q.; Zhou, L.; Yang, Z.; Zhang, Y. (2008). Surface display of GFP by Pseudomonas syringae truncated ice nucleation protein in attenuated Vibrio anguillarum strain. Mar. Biotechnol. 10(6): 701-708. https://dx.doi.org/10.1007/s10126-008-9108-7
In: Marine Biotechnology. Springer-Verlag: New York. ISSN 1436-2228; e-ISSN 1436-2236, more
Peer reviewed article  

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Keywords
    Peptides > Proteins > Marker proteins > Reporter proteins > Green fluorescent protein
    Listonella anguillara (Bergeman, 1909) MacDonell & Colwell, 1985 [WoRMS]
    Marine/Coastal

Authors  Top 
  • Xu, Y.
  • Liu, Q.
  • Zhou, L.
  • Yang, Z.
  • Zhang, Y.

Abstract
    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.

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