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Abstract
Annual Review of Microbiology
Vol. 61: 309-329 (Volume publication date October 2007)
(doi:10.1146/annurev.micro.61.081606.103348)
First published online as a Review in Advance on June 18, 2007
Toward a Hyperstructure Taxonomy*,

Vic Norris,1 ­Tanneke den Blaauwen, ­Roy H. Doi, ­Rasika M. Harshey, ­Laurent Janniere, ­Alfonso Jiménez-Sánchez, ­Ding Jun Jin, ­Petra Anne Levin, ­Eugenia Mileykovskaya, ­Abraham Minsky, ­Gradimir Misevic, ­Camille Ripoll, ­Milton Saier, ­Jr., Kirsten Skarstad, and ­Michel Thellier­
1Department of Science, University of Rouen, 76821 Mont Saint Aignan Cedex, France and Epigenomics Project, genopole®, 91000 Evry, France; email:

Bacterial cells contain many large, spatially extended assemblies of ions, molecules, and macromolecules, called hyperstructures, that are implicated in functions that range from DNA replication and cell division to chemotaxis and secretion. Interactions between these hyperstructures would create a level of organization intermediate between macromolecules and the cell itself. To explore this level, a taxonomy is needed. Here, we describe classification criteria based on the form of the hyperstructure and on the processes responsible for this form. These processes include those dependent on coupled transcription-translation, protein-protein affinities, chromosome site-binding by protein, and membrane structures. Various combinations of processes determine the formation, maturation, and demise of many hyperstructures that therefore follow a trajectory within the space of classification by form/process. Hence a taxonomy by trajectory may be desirable. Finally, we suggest that working toward a taxonomy based on speculative interactions between hyperstructures promises most insight into life at this level.

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Authors:
Vic Norris
Tanneke den Blaauwen
Roy H. Doi
Rasika M. Harshey
Laurent Janniere
Alfonso Jiménez-Sánchez
Ding Jun Jin
Petra Anne Levin
Eugenia Mileykovskaya
Abraham Minsky
Gradimir Misevic
Camille Ripoll
Milton Saier
Jr., Kirsten Skarstad
Michel Thellier
Keywords:
cytoskeleton
cell cycle
module
assembly
bacteria

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