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FlgM as a Secretion Moiety for the Development of an Inducible Type III Secretion System
Authors:Thomas Heel  Georg F. Vogel  Andrea Lammirato  Rainer Schneider  Bernhard Auer
Affiliation:1. Institute of Biochemistry, University of Innsbruck, Innsbruck, Austria.; 2. Austrian Centre of Industrial Biotechnology, Graz, Austria.; 3. Center for Molecular Biosciences (CMBI), University of Innsbruck, Innsbruck, Austria.; 4. Division of Histology and Embryology, Medical University of Innsbruck, Innsbruck, Austria.; 5. Division of Cell Biology, Medical University of Innsbruck, Innsbruck, Austria.; Universidad Nacional Autónoma de México, Mexico,
Abstract: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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