This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Dilks, K.
Right arrow Articles by Pohlschröder, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Dilks, K.
Right arrow Articles by Pohlschröder, M.

 Previous Article  |  Next Article 

Journal of Bacteriology, December 2005, p. 8104-8113, Vol. 187, No. 23
0021-9193/05/$08.00+0     doi:10.1128/JB.187.23.8104-8113.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Genetic and Biochemical Analysis of the Twin-Arginine Translocation Pathway in Halophilic Archaea

Kieran Dilks, María Inés Giménez, and Mechthild Pohlschröder*

Department of Biology, University of Pennsylvania, Philadelphia, Pennsylvania 19104

Received 28 June 2005/ Accepted 15 September 2005

The twin-arginine translocation (Tat) pathway is present in a wide variety of prokaryotes and is capable of exporting partially or fully folded proteins from the cytoplasm. Although diverse classes of proteins are transported via the Tat pathway, in most organisms it facilitates the secretion of a relatively small number of substrates compared to the Sec pathway. However, computational evidence suggests that haloarchaea route nearly all secreted proteins to the Tat pathway. We have expanded previous computational analyses of the haloarchaeal Tat pathway and initiated in vivo characterization of the Tat machinery in a model haloarchaeon, Haloferax volcanii. Consistent with the predicted usage of the this pathway in the haloarchaea, we determined that three of the four identified tat genes in Haloferax volcanii are essential for viability when grown aerobically in complex medium. This represents the first report of an organism that requires the Tat pathway for viability when grown under such conditions. Deletion of the nonessential gene had no effect on the secretion of a verified substrate of the Tat pathway. The two TatA paralogs TatAo and TatAt were detected in both the membrane and cytoplasm and could be copurified from the latter fraction. Using size exclusion chromatography to further characterize cytoplasmic and membrane TatA proteins, we find these proteins present in high-molecular-weight complexes in both cellular fractions.


* Corresponding author. Mailing address: Department of Biology, University of Pennsylvania, Philadelphia, PA 19104. Phone: (215) 573-2278. Fax: (215) 898-8780. E-mail: pohlschr{at}sas.upenn.edu.


Journal of Bacteriology, December 2005, p. 8104-8113, Vol. 187, No. 23
0021-9193/05/$08.00+0     doi:10.1128/JB.187.23.8104-8113.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Sanchez-Porro, C., Mellado, E., Pugsley, A. P., Francetic, O., Ventosa, A. (2009). The Haloprotease CPI Produced by the Moderately Halophilic Bacterium Pseudoalteromonas ruthenica Is Secreted by the Type II Secretion Pathway. Appl. Environ. Microbiol. 75: 4197-4201 [Abstract] [Full Text]  
  • Bagos, P.G., Tsirigos, K.D., Plessas, S.K., Liakopoulos, T.D., Hamodrakas, S.J. (2009). Prediction of signal peptides in archaea. Protein Eng Des Sel 22: 27-35 [Abstract] [Full Text]  
  • Hand, N. J., Klein, R., Laskewitz, A., Pohlschroder, M. (2006). Archaeal and Bacterial SecD and SecF Homologs Exhibit Striking Structural and Functional Conservation. J. Bacteriol. 188: 1251-1259 [Abstract] [Full Text]