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 Hao, J.
Right arrow Articles by Kendrick, K. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hao, J.
Right arrow Articles by Kendrick, K. E.

 Previous Article  |  Next Article 

J Bacteriol, April 1998, p. 2125-2132, Vol. 180, No. 8
0021-9193/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.

Visualization of Penicillin-Binding Proteins during Sporulation of Streptomyces griseus

Jiang Hao and Kathleen E. Kendrick*

Department of Microbiology, Ohio State University, Columbus, Ohio 43210

Received 10 November 1997/Accepted 2 February 1998

We used fluorescein-tagged beta -lactam antibiotics to visualize penicillin-binding proteins (PBPs) in sporulating cultures of Streptomyces griseus. Six PBPs were identified in membranes prepared from growing and sporulating cultures. The binding activity of an 85-kDa PBP increased fourfold by 10 to 12 h of sporulation, at which time the sporulation septa were formed. Cefoxitin inhibited the interaction of the fluorescein-tagged antibiotics with the 85-kDa PBP and also prevented septum formation during sporulation but not during vegetative growth. The 85-kDa PBP, which was the predominant PBP in membranes of cells that were undergoing septation, preferentially bound fluorescein-6-aminopenicillanic acid (Flu-APA). Fluorescence microscopy showed that the sporulation septa were specifically labeled by Flu-APA; this interaction was blocked by prior exposure of the cells to cefoxitin at a concentration that interfered with septation. We hypothesize that the 85-kDa PBP is involved in septum formation during sporulation of S. griseus.


* Corresponding author. Mailing address: Department of Microbiology, 484 West 12th Ave., Ohio State University, Columbus, OH 43210. Phone: (614) 292-1440. Fax: (614) 292-9195 or (614) 292-8120. E-mail: kendrick.1{at}osu.edu.




This article has been cited by other articles:

  • Scheffers, D.-J., Pinho, M. G. (2005). Bacterial Cell Wall Synthesis: New Insights from Localization Studies. Microbiol. Mol. Biol. Rev. 69: 585-607 [Abstract] [Full Text]  
  • Kwak, J., Dharmatilake, A. J., Jiang, H., Kendrick, K. E. (2001). Differential Regulation of ftsZ Transcription during Septation of Streptomyces griseus. J. Bacteriol. 183: 5092-5101 [Abstract] [Full Text]  
  • Kwak, J., McCue, L. A., Trczianka, K., Kendrick, K. E. (2001). Identification and Characterization of a Developmentally Regulated Protein, EshA, Required for Sporogenic Hyphal Branches in Streptomyces griseus. J. Bacteriol. 183: 3004-3015 [Abstract] [Full Text]  
  • Lázaro, S., Fernández-Piñas, F., Fernández-Valiente, E., Blanco-Rivero, A., Leganés, F. (2001). pbpB, a Gene Coding for a Putative Penicillin-Binding Protein, Is Required for Aerobic Nitrogen Fixation in the Cyanobacterium Anabaena sp. Strain PCC7120. J. Bacteriol. 183: 628-636 [Abstract] [Full Text]  
  • van Wezel, G. P., van der Meulen, J., Kawamoto, S., Luiten, R. G. M., Koerten, H. K., Kraal, B. (2000). ssgA Is Essential for Sporulation of Streptomyces coelicolor A3(2) and Affects Hyphal Development by Stimulating Septum Formation. J. Bacteriol. 182: 5653-5662 [Abstract] [Full Text]  
  • Jiang, H., Kendrick, K. E. (2000). Characterization of ssfR and ssgA, Two Genes Involved in Sporulation of Streptomyces griseus. J. Bacteriol. 182: 5521-5529 [Abstract] [Full Text]  
  • Zhao, G., Meier, T. I., Kahl, S. D., Gee, K. R., Blaszczak, L. C. (1999). BOCILLIN FL, a Sensitive and Commercially Available Reagent for Detection of Penicillin-Binding Proteins. Antimicrob. Agents Chemother. 43: 1124-1128 [Abstract] [Full Text]