JB
Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
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 Google Scholar
Google Scholar
Right arrow Articles by Real, G.
Right arrow Articles by Moran, C. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Real, G.
Right arrow Articles by Moran, C. P., Jr.

 Previous Article  |  Next Article 

Journal of Bacteriology, September 2005, p. 6443-6453, Vol. 187, No. 18
0021-9193/05/$08.00+0     doi:10.1128/JB.187.18.6443-6453.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

A Gene Encoding a Holin-Like Protein Involved in Spore Morphogenesis and Spore Germination in Bacillus subtilis

Gonçalo Real,1 Sérgio M. Pinto,1 Ghislain Schyns,2,{dagger} Teresa Costa,1 Adriano O. Henriques,1,2 and Charles P. Moran Jr.2*

Instituto de Tecnologia Química e Biológica, Universidade Nova de Lisboa, Avenida da República, Apartado 127, 2781-901 Oeiras, Portugal,1 Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, Georgia 303222

Received 23 March 2005/ Accepted 25 May 2005

We report here studies of expression and functional analysis of a Bacillus subtilis gene, ywcE, which codes for a product with features of a holin. Primer extension analysis of ywcE transcription revealed that a single transcript accumulated from the onset of sporulation onwards, produced from a {sigma}A-type promoter bearing the TG dinucleotide motif of "extended" –10 promoters. No primer extension product was detected in vivo during growth. However, specific runoff products were produced in vitro from the ywcE promoter by purified {sigma}A-containing RNA polymerase (E{sigma}A), and the in vivo and in vitro transcription start sites were identical. These results suggested that utilization of the ywcE promoter by E{sigma}A during growth was subjected to repression. Studies with a lacZ fusion revealed that the transition-state regulator AbrB repressed the transcription of ywcE during growth. This repression was reversed at the onset of sporulation in a Spo0A-dependent manner, but Spo0A did not appear to contribute otherwise to ywcE transcription. We found ywcE to be required for proper spore morphogenesis. Spores of the ywcE mutant showed a reduced outer coat which lacked the characteristic striated pattern, and the outer coat failed to attach to the underlying inner coat. The mutant spores also accumulated reduced levels of dipicolinic acid. ywcE was also found to be important for spore germination.


* Corresponding author. Mailing address: Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA 30322. Phone: (404) 727-5969. Fax: (404) 727-5993. E-mail: moran{at}microbio.emory.edu.

{dagger} Present address: DSM Nutritional Products, Bau 203/25a, Wurmisweg 576, CH-4303 Kaiseraugst, Switzerland.


Journal of Bacteriology, September 2005, p. 6443-6453, Vol. 187, No. 18
0021-9193/05/$08.00+0     doi:10.1128/JB.187.18.6443-6453.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.







Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
Appl. Environ. Microbiol. Infect. Immun. Eukaryot. Cell
Mol. Cell. Biol. J. Virol. Microbiol. Mol. Biol. Rev.
ALL ASM JOURNALS

Copyright © 2005 by the American Society for Microbiology. All rights reserved.