Journal of Bacteriology, August 2003, p. 4578-4584, Vol. 185, No. 15
0021-9193/03/$08.00+0 DOI: 10.1128/JB.185.15.4578-4584.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.
Molecular and Functional Analysis of the lepB Gene, Encoding a Type I Signal Peptidase from Rickettsia rickettsii and Rickettsia typhi
M. Sayeedur Rahman,* Jason A. Simser, Kevin R. Macaluso, and Abdu F. Azad
Department of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, Maryland 21201
Received 14 March 2003/
Accepted 7 May 2003
The type I signal peptidase lepB genes from Rickettsia rickettsii and Rickettsia typhi, the etiologic agents of Rocky Mountain spotted fever and murine typhus, respectively, were cloned and characterized. Sequence analysis of the cloned lepB genes from R. rickettsii and R. typhi shows open reading frames of 801 and 795 nucleotides, respectively. Alignment analysis of the deduced amino acid sequences reveals the presence of highly conserved motifs that are important for the catalytic activity of bacterial type I signal peptidase. Reverse transcription-PCR and Northern blot analysis demonstrated that the lepB gene of R. rickettsii is cotranscribed in a polycistronic message with the putative nuoF (encoding NADH dehydrogenase I chain F), secF (encoding protein export membrane protein), and rnc (encoding RNase III) genes in a secF-nuoF-lepB-rnc cluster. The cloned lepB genes from R. rickettsii and R. typhi have been demonstrated to possess signal peptidase I activity in Escherichia coli preprotein processing in vivo by complementation assay.
* Corresponding author. Mailing address: Department of Microbiology and Immunology, University of Maryland School of Medicine, 655 West Baltimore St., BRB 13-009, Baltimore, MD 21201. Phone: (410) 706-3337. Fax: (410) 706-0282. E-mail: mrahm001{at}umaryland.edu.
Journal of Bacteriology, August 2003, p. 4578-4584, Vol. 185, No. 15
0021-9193/03/$08.00+0 DOI: 10.1128/JB.185.15.4578-4584.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.
This article has been cited by other articles:
-
Wang, H., Na, B., Yang, H., Tai, P. C.
(2008). Additional In Vitro and In Vivo Evidence for SecA Functioning as Dimers in the Membrane: Dissociation into Monomers Is Not Essential for Protein Translocation in Escherichia coli. J. Bacteriol.
190: 1413-1418
[Abstract]
[Full Text]
-
Rahman, M. S., Ceraul, S. M., Dreher-Lesnick, S. M., Beier, M. S., Azad, A. F.
(2007). The lspA Gene, Encoding the Type II Signal Peptidase of Rickettsia typhi: Transcriptional and Functional Analysis. J. Bacteriol.
189: 336-341
[Abstract]
[Full Text]
-
Edwards, M. T., Rison, S. C. G., Stoker, N. G., Wernisch, L.
(2005). A universally applicable method of operon map prediction on minimally annotated genomes using conserved genomic context. Nucleic Acids Res
33: 3253-3262
[Abstract]
[Full Text]
-
Rahman, M. S., Simser, J. A., Macaluso, K. R., Azad, A. F.
(2005). Functional analysis of secA homologues from rickettsiae. Microbiology
151: 589-596
[Abstract]
[Full Text]
-
Lammertyn, E., Van Mellaert, L., Meyen, E., Lebeau, I., De Buck, E., Anne, J., Geukens, N.
(2004). Molecular and functional characterization of type I signal peptidase from Legionella pneumophila. Microbiology
150: 1475-1483
[Abstract]
[Full Text]
Copyright © 2003 by the American Society for Microbiology. All rights reserved.