2003
DOI: 10.1016/j.tcb.2003.09.005
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A dynamic bacterial cytoskeleton

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Cited by 112 publications
(82 citation statements)
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“…While we are currently undertaking work on a pyrenoid proteome and also investigating the relationship between rubisco structure and function in the chloroplast pyrenoid, our closest guess to the normal pyrenoid structure is some type of aggregation mechanism associated with rubisco, which may be related either to rubisco holoenzyme amino acid residue interactions or some additional plastoskeleton structures. There is evidence for the existence of complex filamentous networks in bacteria (Carballido-Ló pez & Errington 2003), which could have a counterpart in the endosymbiotically inherited plastids or during cell division. At any event, solving the riddle of the pyrenoid structure and operation for installation in C3 plants may provide a more tractable alternative to the introduction of C4 biochemistry into certain crop species.…”
Section: Discussionmentioning
confidence: 99%
“…While we are currently undertaking work on a pyrenoid proteome and also investigating the relationship between rubisco structure and function in the chloroplast pyrenoid, our closest guess to the normal pyrenoid structure is some type of aggregation mechanism associated with rubisco, which may be related either to rubisco holoenzyme amino acid residue interactions or some additional plastoskeleton structures. There is evidence for the existence of complex filamentous networks in bacteria (Carballido-Ló pez & Errington 2003), which could have a counterpart in the endosymbiotically inherited plastids or during cell division. At any event, solving the riddle of the pyrenoid structure and operation for installation in C3 plants may provide a more tractable alternative to the introduction of C4 biochemistry into certain crop species.…”
Section: Discussionmentioning
confidence: 99%
“…Formation of the bacterial division septum is preceded by assembly of a multiprotein septasome complex that is visible as a ring extending around the cell cylinder at the division site (16,19). The septasome is required for invagination of the division septum and subsequent separation of the daughter cells.…”
Section: Ii)mentioning
confidence: 99%
“…The striking observation that depletion or mutational inactivation of both actin homologues ParM and MreB result in a DNA segregation defect, raises the possibility that MreB filaments participate directly or indirectly in chromosome segregation. The discovery that MreB filaments in vivo are dynamic would satisfy a mechanism in which polymerization of MreB would actively move chromosomal DNA in opposite directions toward the cell poles (Carballido-Lopez & Errington 2003;Defeu Soufo & Graumann 2004). Alternatively, MreB filaments may serve as the tracks along which presently unidentified motor proteins move to drive chromosomal origin regions apart.…”
Section: A Link Between Dna Segregation and The Bacterial Cytoskeleton?mentioning
confidence: 99%