Literature DB >> 10733957

Biophysical characterization of changes in amounts and activity of Escherichia coli cell and compartment water and turgor pressure in response to osmotic stress.

D S Cayley1, H J Guttman, M T Record.   

Abstract

To obtain turgor pressure, intracellular osmolalities, and cytoplasmic water activity of Escherichia coli as a function of osmolality of growth, we have quantified and analyzed amounts of cell, cytoplasmic, and periplasmic water as functions of osmolality of growth and osmolality of plasmolysis of nongrowing cells with NaCl. The effects are large; NaCl (plasmolysis) titrations of cells grown in minimal medium at 0.03 Osm reduce cytoplasmic and cell water to approximately 20% and approximately 50% of their original values, and increase periplasmic water by approximately 300%. Independent analysis of amounts of cytoplasmic and cell water demonstrate that turgor pressure decreases with increasing osmolality of growth, from approximately 3.1 atm at 0.03 Osm to approximately 1.5 at 0.1 Osm and to less than 0.5 atm above 0.5 Osm. Analysis of periplasmic membrane-derived oligosaccharide (MDO) concentrations as a function of osmolality, calculated from literature analytical data and measured periplasmic volumes, provides independent evidence that turgor pressure decreases with increasing osmolality, and verifies that cytoplasmic and periplasmic osmolalities are equal. We propose that MDO play a key role in periplasmic volume regulation at low-to-moderate osmolality. At high growth osmolalities, where only a small amount of cytoplasmic water is observed, the small turgor pressure of E. coli demonstrates that cytoplasmic water activity is only slightly less than extracellular water activity. From these findings, we deduce that the activity of cytoplasmic water exceeds its mole fraction at high osmolality, and, therefore, conclude that the activity coefficient of cytoplasmic water increases with increasing growth osmolality and exceeds unity at high osmolality, presumably as a consequence of macromolecular crowding. These novel findings are significant for thermodynamic analyses of effects of changes in growth osmolality on biopolymer processes in general and osmoregulatory processes in particular in the E. coli cytoplasm.

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Year:  2000        PMID: 10733957      PMCID: PMC1300771          DOI: 10.1016/s0006-3495(00)76726-9

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  40 in total

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Authors:  J M Wood
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Authors:  A L Koch
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Authors:  K Sen; J Hellman; H Nikaido
Journal:  J Biol Chem       Date:  1988-01-25       Impact factor: 5.157

5.  Osmotically induced volume and turbidity changes of Escherichia coli due to salts, sucrose and glycerol, with particular reference to the rapid permeation of glycerol into the cell.

Authors:  M M Alemohammad; C J Knowles
Journal:  J Gen Microbiol       Date:  1974-05

6.  Osmotic regulation and the biosynthesis of membrane-derived oligosaccharides in Escherichia coli.

Authors:  E P Kennedy
Journal:  Proc Natl Acad Sci U S A       Date:  1982-02       Impact factor: 11.205

7.  Osmoregulation in Escherichia coli by accumulation of organic osmolytes: betaines, glutamic acid, and trehalose.

Authors:  P I Larsen; L K Sydnes; B Landfald; A R Strøm
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8.  Osmotic regulation of biosynthesis of membrane-derived oligosaccharides in Escherichia coli.

Authors:  E P Kennedy; M K Rumley
Journal:  J Bacteriol       Date:  1988-06       Impact factor: 3.490

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10.  Characterization of the cytoplasm of Escherichia coli K-12 as a function of external osmolarity. Implications for protein-DNA interactions in vivo.

Authors:  S Cayley; B A Lewis; H J Guttman; M T Record
Journal:  J Mol Biol       Date:  1991-11-20       Impact factor: 5.469

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  73 in total

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Authors:  Michael C Konopka; Irina A Shkel; Scott Cayley; M Thomas Record; James C Weisshaar
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7.  The osmolyte TMAO stabilizes native RNA tertiary structures in the absence of Mg2+: evidence for a large barrier to folding from phosphate dehydration.

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Journal:  J Mol Biol       Date:  2010-09-25       Impact factor: 5.469

8.  Reduction of turgor is not the stimulus for the sensor kinase KdpD of Escherichia coli.

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Journal:  J Bacteriol       Date:  2008-02-01       Impact factor: 3.490

9.  Distribution of mechanical stress in the Escherichia coli cell envelope.

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10.  Cytoplasmic protein mobility in osmotically stressed Escherichia coli.

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