Monitoring Chromosome Dynamics in a Living Bacterial Cell

The organization of chromosomes of bacteria, even for the heavily studied case of E. coli, is cloaked in mystery. Using fluorescently-tagged chromosome-organizing proteins, NU-MRSEC researchers have developed techniques to directly visualize the chromosome inside a living E. coli cell, following its progeny as it divides to form a “microcolony”. These methods will be used to analyze how the chromosome foldes and divides, what the role of specific proteins is in maintaining its shape, and how chromosome folding mediated by those proteins affects expression of genes and the operation of cell metabolic processes. Applications include improvement of genetic “programming” of cells for biomaterial production.

chromosome

Top row: cell dividing, early stage of microcolony.
Middle row: chromosome inside cell visualized using a fluorescent chromosome protein (gfp-Fis).
Bottom left: membrane and chromosome following division, note asymmetric positioning. Bottom center: chromosome in cell.
Bottom right: isolated from cell for micromanipulation study; note expansion.

 

Nastaran Hadizadeh, John F. Marko

Collaborators: Calin Guet and Philippe Cluzel, Harvard University; Reid Johnson, UCLA.

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The Materials Research Science and Engineering Center (MRSEC) is supported by the National Science Foundation under NSF Award Number DMR-0520513. Any opinions, findings and conclusions or recommendations expressed in this material are those of the author(s) and do not necessarily reflect those of the National Science Foundation.
© 2008 Northwestern University