Transertion and cell geometry organize the Escherichia coli nucleoid during rapid growth
Preprint
Abstract
A bstract: Bacterial chromosomes are spatiotemporally organized and sensitive to environmental changes. However, the mechanisms underlying chromosome configuration and reorganization are currently not fully understood. Using 3D single-molecule localization microscopy and live-cell imaging, we show that the Escherichia coli nucleoid adopts a condensed, membrane-associated configuration during rapid growth. To study the influence of different biosynthetic processes on nucleoid morphology and positioning, we recorded multi-colour super-resolution images during drug treatment. After developing analysis routines for confocal and super-resolution images, we captured highly resolved snapshots which revealed the complete loss of the membrane-bound state of the nucleoid within 10 minutes of halting transcription and translation. This indicates an active role of transertion (coupled transcription, translation and membrane insertion) in nucleoid organization. In contrast, cell wall synthesis inhibition only affects nucleoid organization during morphological changes. Further, we provide evidence that the E. coli nucleoid spatially correlates with MreB in unperturbed E. coli cells, while this correlation diminishes in cells with changed cell geometry or upon inhibition of protein biosynthesis. Replication inhibition experiments, as well as multi-drug treatments highlight the role of entropic effects and transcription in nucleoid condensation and positioning. In summary, we provide experimental evidence for transertion as a principal organiser of the bacterial nucleoid, and show that an altered metabolic state and antibiotic treatment both lead to major changes in the degree of transertion and overall spatial organization of the nucleoid. Our high-resolution characterization reveals dynamics of antibiotic action and provides tools to quantify bacterial chromosome organization. This does not only provide valuable insights into the role of transertion, but can also be applied to study other cell-biological processes.Keywords
This publication has 72 references indexed in Scilit:
- Physical manipulation of the Escherichia coli chromosome reveals its soft natureProceedings of the National Academy of Sciences, 2012
- Fiji: an open-source platform for biological-image analysisNature Methods, 2012
- Membrane protein expression triggers chromosomal locus repositioning in bacteriaProceedings of the National Academy of Sciences, 2012
- Live Cell Imaging of Bacillus subtilis and Streptococcus pneumoniae using Automated Time-lapse MicroscopyJournal of Visualized Experiments, 2011
- Cooperation Between Translating Ribosomes and RNA Polymerase in Transcription ElongationScience, 2010
- MreB Drives De N ovo Rod Morphogenesis in Caulobacter crescentus via Remodeling of the Cell WallJournal of Bacteriology, 2010
- Bacterial translation elongation factor EF-Tu interacts and colocalizes with actin-like MreB proteinProceedings of the National Academy of Sciences, 2010
- Wide-field subdiffraction imaging by accumulated binding of diffusing probesProceedings of the National Academy of Sciences, 2006
- The depletion attraction: an underappreciated force driving cellular organizationJournal of Cell Biology, 2006
- Entropy-driven spatial organization of highly confined polymers: Lessons for the bacterial chromosomeProceedings of the National Academy of Sciences, 2006