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Streptomyces: A Screening Tool for Bacterial Cell Division Inhibitors
- Publication Year :
- 2015
- Publisher :
- SAGE Publications, 2015.
-
Abstract
- Cell division is essential for spore formation but not for viability in the filamentous streptomycetes bacteria. Failure to complete cell division instead blocks spore formation, a phenotype that can be visualized by the absence of gray (in Streptomyces coelicolor) and green (in Streptomyces venezuelae) spore-associated pigmentation. Despite the lack of essentiality, the streptomycetes divisome is similar to that of other prokaryotes. Therefore, the chemical inhibitors of sporulation in model streptomycetes may interfere with the cell division in rod-shaped bacteria as well. To test this, we investigated 196 compounds that inhibit sporulation in S. coelicolor. We show that 19 of these compounds cause filamentous growth in Bacillus subtilis, consistent with impaired cell division. One of the compounds is a DNA-damaging agent and inhibits cell division by activating the SOS response. The remaining 18 act independently of known stress responses and may therefore act on the divisome or on divisome positioning and stability. Three of the compounds (Fil-1, Fil-2, and Fil-3) confer distinct cell division defects on B. subtilis. They also block B. subtilis sporulation, which is mechanistically unrelated to the sporulation pathway of streptomycetes but is also dependent on the divisome. We discuss ways in which these differing phenotypes can be used in screens for cell division inhibitors.
- Subjects :
- Streptomyces venezuelae
Cell division
biology
Streptomyces coelicolor
fungi
Drug Evaluation, Preclinical
Microbial Sensitivity Tests
Bacillus subtilis
biology.organism_classification
Biochemistry
Streptomyces
Article
Bacterial cell structure
Anti-Bacterial Agents
Analytical Chemistry
Microbiology
Cell biology
Small Molecule Libraries
Molecular Medicine
SOS response
SOS Response, Genetics
Cell Division
Bacteria
Biotechnology
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....9226b258f9882a1a7d69862ef66de5a8