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Improved methods for producing outer membrane vesicles in Gram-negative bacteria
被引:61
作者:

Henry, T
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机构: CNRS, Inst Biol Struct & Microbiol, UPR 9027, F-13402 Marseille 20, France

Pommier, S
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机构: CNRS, Inst Biol Struct & Microbiol, UPR 9027, F-13402 Marseille 20, France

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Bernadac, A
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机构: CNRS, Inst Biol Struct & Microbiol, UPR 9027, F-13402 Marseille 20, France

Gorvel, JP
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h-index: 0
机构: CNRS, Inst Biol Struct & Microbiol, UPR 9027, F-13402 Marseille 20, France

Lloubès, R
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h-index: 0
机构: CNRS, Inst Biol Struct & Microbiol, UPR 9027, F-13402 Marseille 20, France
机构:
[1] CNRS, Inst Biol Struct & Microbiol, UPR 9027, F-13402 Marseille 20, France
[2] Ctr Immunol Marseille Luminy, Case 906, F-13288 Marseille 9, France
[3] Univ Basel, Biozentrum, CH-4056 Basel, Switzerland
关键词:
outer membrane vesicles;
outer membrane integrity;
Tol-Pal proteins;
colicins;
minor coat g3p protein;
D O I:
10.1016/j.resmic.2004.04.007
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Outer membrane vesicle formation occurs during Gram-negative bacterial growth. However, natural production of large amounts of outer membrane vesicles has only been described in a few bacterial genera. The purified vesicles of some bacterial pathogens have shown potential applications in vaccinology and in antibiotic therapy. This study focused on the development of a gene expression system able to induce production of large amounts of outer membrane vesicles. The Tol-Pal system of Escherichia coli, required to maintain outer membrane integrity, is composed of five cell envelope proteins, TolA, TolB, TolQ, TolR and Pal. Tol proteins are parasitized by filamentous bacteriophages and by colicins. The phage infection process and colicin import require, respectively, the N-terminal domain of the minor coat g3p protein and the translocation domain of colicins, with both domains interacting with Tol proteins. In this study, we show that the periplasmic production of either Tol, g3p or colicin domains was able to specifically destabilize the E. coli or Shigella flexneri cell envelope and to induce production of high amounts of vesicles. This technique was further found to work efficiently in Salmonella enterica serovar Typhimurium. (C) 2004 Elsevier SAS. All rights reserved.
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页码:437 / 446
页数:10
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Bernadac, A
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