Novel surface display system for proteins on non-genetically modified gram-positive bacteria

Appl Environ Microbiol. 2006 Jan;72(1):880-9. doi: 10.1128/AEM.72.1.880-889.2006.

Abstract

A novel display system is described that allows highly efficient immobilization of heterologous proteins on bacterial surfaces in applications for which the use of genetically modified bacteria is less desirable. This system is based on nonliving and non-genetically modified gram-positive bacterial cells, designated gram-positive enhancer matrix (GEM) particles, which are used as substrates to bind externally added heterologous proteins by means of a high-affinity binding domain. This binding domain, the protein anchor (PA), was derived from the Lactococcus lactis peptidoglycan hydrolase AcmA. GEM particles were typically prepared from the innocuous bacterium L. lactis, and various parameters for the optimal preparation of GEM particles and binding of PA fusion proteins were determined. The versatility and flexibility of the display and delivery technology were demonstrated by investigating enzyme immobilization and nasal vaccine applications.

Publication types

  • Evaluation Study

MeSH terms

  • Administration, Intranasal
  • Animals
  • Female
  • Immunization
  • Lactococcus lactis / genetics*
  • Lactococcus lactis / metabolism*
  • Malaria / prevention & control
  • Malaria Vaccines
  • Mice
  • Mice, Inbred BALB C
  • N-Acetylmuramoyl-L-alanine Amidase / genetics
  • N-Acetylmuramoyl-L-alanine Amidase / metabolism*
  • Plasmodium berghei / genetics
  • Plasmodium berghei / immunology
  • Plasmodium berghei / metabolism
  • Protozoan Proteins / genetics
  • Protozoan Proteins / metabolism*
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism*

Substances

  • Malaria Vaccines
  • Protozoan Proteins
  • Recombinant Fusion Proteins
  • circumsporozoite protein, Protozoan
  • N-Acetylmuramoyl-L-alanine Amidase