Literature DB >> 10572306

Hypothesis: hyperstructures regulate bacterial structure and the cell cycle.

V Norris1, S Alexandre, Y Bouligand, D Cellier, M Demarty, G Grehan, G Gouesbet, J Guespin, E Insinna, L Le Sceller, B Maheu, C Monnier, N Grant, T Onoda, N Orange, A Oshima, L Picton, H Polaert, C Ripoll, M Thellier, J M Valleton, M C Verdus, J C Vincent, G White, P Wiggins.   

Abstract

A myriad different constituents or elements (genes, proteins, lipids, ions, small molecules etc.) participate in numerous physico-chemical processes to create bacteria that can adapt to their environments to survive, grow and, via the cell cycle, reproduce. We explore the possibility that it is too difficult to explain cell cycle progression in terms of these elements and that an intermediate level of explanation is needed. This level is that of hyperstructures. A hyperstructure is large, has usually one particular function, and contains many elements. Non-equilibrium, or even dissipative, hyperstructures that, for example, assemble to transport and metabolize nutrients may comprise membrane domains of transporters plus cytoplasmic metabolons plus the genes that encode the hyperstructure's enzymes. The processes involved in the putative formation of hyperstructures include: metabolite-induced changes to protein affinities that result in metabolon formation, lipid-organizing forces that result in lateral and transverse asymmetries, post-translational modifications, equilibration of water structures that may alter distributions of other molecules, transertion, ion currents, emission of electromagnetic radiation and long range mechanical vibrations. Equilibrium hyperstructures may also exist such as topological arrays of DNA in the form of cholesteric liquid crystals. We present here the beginning of a picture of the bacterial cell in which hyperstructures form to maximize efficiency and in which the properties of hyperstructures drive the cell cycle.

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Year:  1999        PMID: 10572306     DOI: 10.1016/s0300-9084(99)00203-5

Source DB:  PubMed          Journal:  Biochimie        ISSN: 0300-9084            Impact factor:   4.079


  5 in total

1.  Effects of calcium and calcium chelators on growth and morphology of Escherichia coli L-form NC-7.

Authors:  T Onoda; J Enokizono; H Kaya; A Oshima; P Freestone; V Norris
Journal:  J Bacteriol       Date:  2000-03       Impact factor: 3.490

2.  Examining the architecture of cellular computing through a comparative study with a computer.

Authors:  Degeng Wang; Michael Gribskov
Journal:  J R Soc Interface       Date:  2005-06-22       Impact factor: 4.118

3.  Question 7: the first units of life were not simple cells.

Authors:  Vic Norris; Axel Hunding; Francois Kepes; Doron Lancet; Abraham Minsky; Derek Raine; Robert Root-Bernstein; K Sriram
Journal:  Orig Life Evol Biosph       Date:  2007-07-10       Impact factor: 1.950

Review 4.  Functional taxonomy of bacterial hyperstructures.

Authors:  Vic Norris; Tanneke den Blaauwen; Armelle Cabin-Flaman; Roy H Doi; Rasika Harshey; Laurent Janniere; Alfonso Jimenez-Sanchez; Ding Jun Jin; Petra Anne Levin; Eugenia Mileykovskaya; Abraham Minsky; Milton Saier; Kirsten Skarstad
Journal:  Microbiol Mol Biol Rev       Date:  2007-03       Impact factor: 11.056

5.  Differences in the degree of inhibition of NDP reductase by chemical inactivation and by the thermosensitive mutation nrdA101 in Escherichia coli suggest an effect on chromosome segregation.

Authors:  José Riola; Estrella Guarino; Elena C Guzmán; Alfonso Jiménez-Sánchez
Journal:  Cell Mol Biol Lett       Date:  2006-11-24       Impact factor: 5.787

  5 in total

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