Effect on solute size on diffusion rates through the transmembrane pores of the outer membrane of Escherichia coli

Nutrients usually cross the outer membrane of Escherichia coli by diffusion through water-filled channels surrounded by a specific class of protein, porins. In this study, the rates of diffusion of hydrophilic nonelectrolytes, mostly sugars and sugar alcohols, through the porin channels were determined in two systems, (a) vesicles reconstituted from phospholipids and purified porin and (b) intact cells of mutant strains that produce many fewer porin molecules than wild-type strains. The diffusion rates were strongly affected by the size of the solute, even when the size was well within the "exclusion limit" of the channel. In both systems, hexoses and hexose disaccharides diffused through the channel at rates 50-80% and 2-4%, respectively, of that of a pentose, arabinose. Application of the Renkin equation to these data led to the estimate that the pore radius is approximately 0.6 nm, if the pore is assumed to be a hollow cylinder. The results of the study also show that the permeability of the outer membrane of the wild-type E. coli cell to glucose and lactose can be explained by the presence of porin channels, that a significant fraction of these channels must be functional or "open" under our conditions of growth, and that even 10(5) channels per cell could become limiting when E. coli tries to grow at a maximal rate on low concentrations of slowly penetrating solutes, such as disaccharides.

[1]  H. Nikaido,et al.  Specificity of diffusion channels produced by lambda phage receptor protein of Escherichia coli. , 1980, Proceedings of the National Academy of Sciences of the United States of America.

[2]  K. Meyenburg Transport-Limited Growth Rates in a Mutant of Escherichia coli , 1971 .

[3]  A C Steven,et al.  Ultrastructure of a periodic protein layer in the outer membrane of Escherichia coli , 1977, The Journal of cell biology.

[4]  A. K. Solomon,et al.  Temperature Dependence of Nonelectrolyte Permeation across Red Cell Membranes , 1973, The Journal of general physiology.

[5]  E. M. Renkin,et al.  FILTRATION, DIFFUSION, AND MOLECULAR SIEVING THROUGH POROUS CELLULOSE MEMBRANES , 1954, The Journal of general physiology.

[6]  J. Rosenbusch Characterization of the major envelope protein from Escherichia coli. Regular arrangement on the peptidoglycan and unusual dodecyl sulfate binding. , 1974, The Journal of biological chemistry.

[7]  A. Glauert,et al.  The topography of the bacterial cell wall. , 1969, Annual review of microbiology.

[8]  T. Nakae Outer membrane of Salmonella. Isolation of protein complex that produces transmembrane channels. , 1976, The Journal of biological chemistry.

[9]  O. Maaløe,et al.  DNA replication and the division cycle in Escherichia coli , 1967 .

[10]  B. Bachmann,et al.  Linkage map of Escherichia coli K-12, edition 6. , 1980, Microbiological reviews.

[11]  T. Nakae,et al.  The outer membrane of Gram-negative bacteria. , 1979, Advances in microbial physiology.

[12]  T. Nakae,et al.  Characterization of porins from the outer membrane of Salmonella typhimurium. 2. Physical properties of the functional oligomeric aggregates. , 1979, European journal of biochemistry.

[13]  H. Nikaido,et al.  Outer membrane of gram-negative bacteria. XII. Molecular-sieving function of cell wall , 1976, Journal of bacteriology.

[14]  G. Ames,et al.  Membranes and Transport , 1973 .

[15]  J. Rosenbusch,et al.  Matrix protein from Escherichia coli outer membranes forms voltage-controlled channels in lipid bilayers. , 1978, Proceedings of the National Academy of Sciences of the United States of America.

[16]  T. Nakae,et al.  Transmembrane permeability channels in vesicles reconstituted from single species of porins from Salmonella typhimurium , 1978, Journal of bacteriology.

[17]  Winfried Boos,et al.  Maltose Transport in Escherichia coli K12 , 1976 .

[18]  S. Mizushima,et al.  Characterization of major outer membrane proteins O-8 and O-9 of Escherichia coli K-12. Evidence that structural genes for the two proteins are different. , 1978, Journal of biochemistry.

[19]  R. W. Hogg,et al.  A comparison of the L-arabinose- and D-galactose-binding proteins of Escherichia coli B-r. , 1974, Journal of Biological Chemistry.

[20]  J. Lutkenhaus Role of a major outer membrane protein in Escherichia coli , 1977, Journal of bacteriology.

[21]  E. J. V. van Zoelen,et al.  A molecular basis for an irreversible thermodynamic description on non-electrolyte permeation through lipid bilayers. , 1978, Biochimica et biophysica acta.

[22]  von Meyenburg Kaspar Transport-limited growth rates in a mutant of Escherichia coli. , 1971, Journal of bacteriology.

[23]  A. K. Solomon,et al.  Determination of the Effective Hydrodynamic Radii of Small Molecules by Viscometry , 1961, The Journal of general physiology.

[24]  A. Kotyk Membranes and transport. , 1977, Acta biochimica et biophysica; Academiae Scientiarum Hungaricae.

[25]  T. Sato,et al.  Chromosomal location and expression of the structural gene for major outer membrane protein Ia of Escherichia coli K-12 and of the homologous gene of Salmonella typhimurium , 1979, Journal of bacteriology.

[26]  A. K. Solomon,et al.  Determination of Urea Permeability in Red Cells by Minimum Method , 1970, The Journal of general physiology.

[27]  J. Folch,et al.  A simple method for the isolation and purification of total lipides from animal tissues. , 1957, The Journal of biological chemistry.

[28]  E. Lin,et al.  CAPTURE OF GLYCEROL BY CELLS OF ESCHERICHIA COLI. , 1965, Biochimica et biophysica acta.

[29]  A. Katchalsky,et al.  Thermodynamic analysis of the permeability of biological membranes to non-electrolytes. , 1958, Biochimica et biophysica acta.

[30]  H. Nikaido,et al.  Outer membrane of Salmonella typhimurium: chemical analysis and freeze-fracture studies with lipopolysaccharide mutants , 1975, Journal of bacteriology.

[31]  A. L. Koch,et al.  The adaptive responses of Escherichia coli to a feast and famine existence. , 1971, Advances in microbial physiology.

[32]  R. Benz,et al.  Formation of large, ion-permeable membrane channels by the matrix protein (porin) of Escherichia coli. , 1978, Biochimica et biophysica acta.

[33]  T. Nakae,et al.  Identification of the outer membrane protein of E. coli that produces transmembrane channels in reconstituted vesicle membranes. , 1976, Biochemical and biophysical research communications.