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Journal of Bacteriology, November 2005, p. 7667-7679, Vol. 187, No. 22
0021-9193/05/$08.00+0     doi:10.1128/JB.187.22.7667-7679.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

The Twin-Arginine Translocation Pathway of Mycobacterium smegmatis Is Functional and Required for the Export of Mycobacterial ß-Lactamases

Justin A. McDonough,1 Kari E. Hacker,1 Anthony R. Flores,2 Martin S. Pavelka Jr,2 and Miriam Braunstein1*

Department of Microbiology and Immunology, University of North Carolina School of Medicine, Chapel Hill, North Carolina 27599-7290,1 Department of Microbiology and Immunology, University of Rochester School of Medicine and Dentistry, Rochester, New York 146422

Received 29 June 2005/ Accepted 24 August 2005

The twin-arginine translocation (Tat) pathway exports folded proteins across the bacterial cytoplasmic membrane and is responsible for the proper extracytoplasmic localization of proteins involved in a variety of cellular functions, including pathogenesis. The Mycobacterium tuberculosis and Mycobacterium smegmatis genomes contain open reading frames with homology to components of the Tat export system (TatABC) as well as potential Tat-exported proteins possessing N-terminal signal sequences with the characteristic twin-arginine motif. Due to the importance of exported virulence factors in the pathogenesis of M. tuberculosis and the limited understanding of mycobacterial protein export systems, we sought to determine the functional nature of the Tat export pathway in mycobacteria. Here we describe phenotypic analyses of {Delta}tatA and {Delta}tatC deletion mutants of M. smegmatis, which demonstrated that tatA and tatC encode components of a functional Tat system capable of exporting characteristic Tat substrates. Both mutants displayed a growth defect on agar medium and hypersensitivity to sodium dodecyl sulfate. The mutants were also defective in the export of active ß-lactamases of M. smegmatis (BlaS) and M. tuberculosis (BlaC), both of which possess twin-arginine signal sequences. The Tat-dependent nature of BlaC was further revealed by mutation of the twin-arginine motif. Finally, we demonstrated that replacement of the native signal sequence of BlaC with the predicted Tat signal sequences of M. tuberculosis phospholipase C proteins (PlcA and PlcB) resulted in the Tat-dependent export of an enzymatically active 'BlaC. Thus, 'BlaC can be used as a genetic reporter for Tat-dependent export in mycobacteria.

* Corresponding author. Mailing address: Department of Microbiology and Immunology, CB no. 7290, 804 Mary Ellen Jones, University of North Carolina, Chapel Hill, NC 27599-7290. Phone: (919) 966-5051. Fax: (919) 962-8103. E-mail: Miriam_Braunstein{at}med.unc.edu.

Journal of Bacteriology, November 2005, p. 7667-7679, Vol. 187, No. 22
0021-9193/05/$08.00+0     doi:10.1128/JB.187.22.7667-7679.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.



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