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Control of wall band splitting in Streptococcus faecalis
Journal of General Microbiology
|April 1, 1984
Summary
This study analyzed the cell cycle of Streptococcus faecalis, finding that cell division initiates when growth zones can't keep pace with cytoplasmic production. Pole time closely matches mass doubling time, indicating dichotomous replication.
Area of Science:
- Microbiology
- Cell Biology
- Bacterial Growth Dynamics
Background:
- Understanding bacterial cell cycle regulation is crucial for comprehending growth and division.
- Streptococcus faecalis serves as a model organism for studying microbial cell division.
Purpose of the Study:
- To analyze the cell cycle of Streptococcus faecalis under different growth conditions.
- To estimate cell cycle phase durations and key timing parameters like pole time.
- To investigate the relationship between cell growth, DNA replication, and division.
Main Methods:
- Computerized reconstruction and analysis of whole-mounted, shadowed Streptococcus faecalis cells.
- Application of a novel method for estimating cell cycle phase durations and statistical parameters.
- Classification of cells based on septal radius, growth zones, and 'birth site' characteristics.
Main Results:
- Pole time was found to be only slightly greater than the mass doubling time in both slow and rapid growth conditions.
- In slow-growing cells, 69% of newborn cells lacked growth zones, compared to 16% or less in rapid growth.
- Dichotomous replication occurs, where new DNA synthesis rounds begin before previous ones complete, due to DNA synthesis duration exceeding mass doubling time.
Conclusions:
- Cell division is initiated when surface area expansion via growth zones cannot accommodate cytoplasmic production.
- Initiation of DNA replication and cell wall band splitting are not simultaneous events.
- The cell cycle regulation in Streptococcus faecalis involves complex coordination between growth, DNA replication, and division processes.