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FlgM as a Secretion Moiety for the Development of an Inducible Type III Secretion System
Author(s) -
Thomas Heel,
Georg F. Vogel,
Andrea Lammirato,
Rainer Schneider,
Bernhard Auer
Publication year - 2013
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0059034
Subject(s) - secretion , heterologous , microbiology and biotechnology , escherichia coli , biology , morphogenesis , proteases , recombinant dna , heterologous expression , mutant , model organism , organism , gene , biochemistry , genetics , enzyme
Regulation and assembly of the flagellar type III secretion system is one of the most investigated and best understood regulational cascades in molecular biology. Depending on the host organism, flagellar morphogenesis requires the interplay of more than 50 genes. Direct secretion of heterologous proteins to the supernatant is appealing due to protection against cellular proteases and simplified downstream processing. As Escherichia coli currently remains the predominant host organism used for recombinant prokaryotic protein expression, the generation of a strain that exhibits inducible flagellar secretion would be highly desirable for biotechnological applications. Here, we report the first engineered Escherichia coli mutant strain featuring flagellar morphogenesis upon addition of an external inducer. Using FlgM as a sensor for direct secretion in combination with this novel strain may represent a potent tool for significant improvements in future engineering of an inducible type III secretion for heterologous proteins.

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