Regulation of envelope protein composition during adaptation to osmotic stress in Escherichia coli

Adaptation to osmotic stress alters the amounts of several specific proteins in the Escherichia coli K-12 envelope. The most striking feature of the response to elevated osmolarity was the strong induction of a periplasmic protein with an Mr of 31,000. This protein was absent in mutants with lambda plac Mu insertions in an osmotically inducible locus mapping near 58 min. The insertions are likely to be in proU, a locus encoding a transport activity for the osmoprotectants glycine betaine and proline. Factors affecting the extent of proU induction were identified by direct examination of periplasmic proteins on sodium dodecyl sulfate gels and by measuring beta-galactosidase activity from proU-lac fusions. Expression was stimulated by increasing additions of salt or sucrose to minimal medium, up to a maximum at 0.5 M NaCl. Exogenous glycine betaine acted as an osmoregulatory signal; its addition to the high-osmolarity medium substantially repressed the expression of the 31,000-dalton periplasmic protein and the proU-lac+ fusions. Elevated osmolarity also caused the appearance of a second periplasmic protein (Mr = 16,000), and severe reduction in the amounts of two others. In the outer membrane, the well-characterized repression of OmpF by high osmolarity was observed and was reversed by glycine betaine. Additional changes in membrane composition were also responsive to glycine betaine regulation.

[1]  J. Cairney,et al.  Osmoregulation of Gene Expression in Salmonella typhimurium: proU Encodes an Osmotically Induced Betaine Transport System , 1986, Journal of bacteriology.

[2]  J. Cairney,et al.  Salmonella typhimurium proP gene encodes a transport system for the osmoprotectant betaine , 1985, Journal of bacteriology.

[3]  J. Gowrishankar,et al.  Identification of osmoresponsive genes in Escherichia coli: evidence for participation of potassium and proline transport systems in osmoregulation , 1985, Journal of bacteriology.

[4]  J. Meury,et al.  Turgor-controlled K+ fluxes and their pathways in Escherichia coli. , 1985, European journal of biochemistry.

[5]  L. Csonka,et al.  Osmotic regulation of L-proline transport in Salmonella typhimurium , 1985, Journal of bacteriology.

[6]  D. Dietzler,et al.  Restoration of cell volume and the reversal of carbohydrate transport and growth inhibition of osmotically upshocked Escherichia coli. , 1985, Biochemical and biophysical research communications.

[7]  D. le Rudulier,et al.  Glycine betaine transport in Escherichia coli: osmotic modulation , 1985, Journal of bacteriology.

[8]  D. Clark,et al.  Proteins induced by high osmotic pressure in Escherichia coli , 1984 .

[9]  L. Enquist,et al.  Experiments With Gene Fusions , 1984 .

[10]  A. Dandekar,et al.  Molecular Biology of Osmoregulation , 1984, Science.

[11]  G. Weinstock,et al.  Lambda placMu: a transposable derivative of bacteriophage lambda for creating lacZ protein fusions in a single step , 1984, Journal of bacteriology.

[12]  S. Granett,et al.  Osmoregulation of alkaline phosphatase synthesis in Escherichia coli K-12 , 1983, Journal of bacteriology.

[13]  D. le Rudulier,et al.  Glycine betaine, an osmotic effector in Klebsiella pneumoniae and other members of the Enterobacteriaceae , 1983, Applied and environmental microbiology.

[14]  M. E. Clark,et al.  Living with water stress: evolution of osmolyte systems. , 1982, Science.

[15]  L. Csonka A third L-proline permease in Salmonella typhimurium which functions in media of elevated osmotic strength , 1982, Journal of bacteriology.

[16]  M. Hall,et al.  The ompB locus and the regulation of the major outer membrane porin proteins of Escherichia coli K12. , 1981, Journal of molecular biology.

[17]  T. Mizuno,et al.  Influence of molecular size and osmolarity of sugars and dextrans on the synthesis of outer membrane proteins O-8 and O-9 of Escherichia coli K-12 , 1979, Journal of bacteriology.

[18]  A. Pugsley,et al.  Identification of three genes controlling production of new outer membrane pore proteins in Escherichia coli K-12 , 1978, Journal of bacteriology.

[19]  M. Casadaban,et al.  Transposition and fusion of the lac genes to selected promoters in Escherichia coli using bacteriophage lambda and Mu. , 1976, Journal of molecular biology.

[20]  W. Epstein,et al.  Cation transport in Escherichia coli. VIII. Potassium transport mutants , 1976, The Journal of general physiology.

[21]  J. C. Measures Role of amino acids in osmoregulation of non-halophilic bacteria , 1975, Nature.

[22]  M. Lederman,et al.  Multiple Transport Components for Putrescine in Escherichia coli , 1974, Journal of bacteriology.

[23]  U. K. Laemmli,et al.  Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 , 1970, Nature.

[24]  S. Schultz,et al.  Cation Transport in Escherichia coli , 1966, The Journal of general physiology.

[25]  S. Schultz,et al.  Cation Transport in Escherichia coli , 1965, The Journal of general physiology.

[26]  A. K. Solomon,et al.  Cation Transport in Escherichia coli , 1966, The Journal of general physiology.

[27]  W. Epstein,et al.  Osmotic control of kdp operon expression in Escherichia coli. , 1981, Proceedings of the National Academy of Sciences of the United States of America.

[28]  Jeffrey H. Miller Experiments in molecular genetics , 1972 .