Tobramycin uptake in Escherichia coli is driven by either electrical potential or ATP

Aminoglycoside antibiotics such as streptomycin and tobramycin must traverse the bacterial cytoplasmic membrane prior to initiating lethal effects. Previous data on Escherichia coli, Staphylococcus aureus, and Bacillus subtilis have demonstrated that transport of aminoglycosides is regulated by delta psi, the electrical component of the proton motive force. However, several laboratories have observed that growth of bacterial cells can occur in the apparent absence of delta psi, and we wished to confirm these studies with E. coli and further investigate whether transport of aminoglycosides could occur in the absence of a membrane potential. Treatment of acrA strain CL2 with the protonophore carbonyl cyanide m-chlorophenylhydrazone (CCCP) dissipated delta psi, decreased intracellular ATP levels, and resulted in cessation of growth; after a variable period of time (3 to 7 h), growth resumed, ultimately achieving growth rates comparable to those of untreated cells. Absence of delta psi in these cells was confirmed by absence of [3H]tetraphenyl phosphonium+ uptake as measured by membrane filtration, lack of flagellar motion, and inability of these cells to transport proline (but not methionine). Regrowth was associated with restoration of normal intracellular ATP as measured by luciferin-luciferase bioluminescence assay. Unlike unacclimatized CL2 cells treated with CCCP, these cells transported [3H]tobramycin similarly to untreated cells; aminoglycoside-induced killing was seen in association with transport. These studies suggest that under certain circumstances aminoglycoside transport can be driven by ATP (or other high-energy activated phosphate donors) alone, in the absence of a measurable delta psi. delta uncBC mutants of CL2 incapable of interconverting delta psi and ATP were treated with CCCP, resulting in dissipation of delta psi but no alteration in ATP content. Despite maintenance of normal ATP, there was no transport of [3H] bramycin, confirming that under normal growth conditions ATP has no role in the transport of aminoglycosides.

[1]  T. A. Krulwich,et al.  Uncoupler-resistant mutants of bacteria. , 1990, Microbiological reviews.

[2]  I. Campbell,et al.  Uncoupler resistance in Escherichia coli: the role of cellular respiration. , 1989, Journal of general microbiology.

[3]  V. Skulachev,et al.  The Na+‐motive respiration in Escherichia coli , 1989 .

[4]  W. Nichols,et al.  Bioenergetics of dihydrostreptomycin transport by Escherichia coli , 1988, FEBS letters.

[5]  P. Tai,et al.  Effects of nucleotides on ATP-dependent protein translocation into Escherichia coli membrane vesicles , 1986, Journal of bacteriology.

[6]  M. Ballesteros,et al.  Respiration rate, growth rate and the accumulation of streptomycin in Escherichia coli. , 1985, Journal of general microbiology.

[7]  P. Tai,et al.  ATP is essential for protein translocation into Escherichia coli membrane vesicles. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[8]  H. Kobayashi,et al.  Proton motive force is not obligatory for growth of Escherichia coli , 1984, Journal of bacteriology.

[9]  J. Cairney,et al.  Proline uptake through the major transport system of Salmonella typhimurium is coupled to sodium ions , 1984, Journal of bacteriology.

[10]  E. Bakker,et al.  The requirement for energy during export of beta‐lactamase in Escherichia coli is fulfilled by the total protonmotive force. , 1984, EMBO Journal.

[11]  H. Kaback,et al.  Quantitative association between electrical potential across the cytoplasmic membrane and early gentamicin uptake and killing in Staphylococcus aureus , 1984, Journal of bacteriology.

[12]  L. Bryan,et al.  Roles of ribosomal binding, membrane potential, and electron transport in bacterial uptake of streptomycin and gentamicin , 1983, Antimicrobial Agents and Chemotherapy.

[13]  H. Kaback,et al.  Membrane potential in anaerobically growing Staphylococcus aureus and its relationship to gentamicin uptake , 1983, Antimicrobial Agents and Chemotherapy.

[14]  H. Kaback,et al.  Membrane potential and gentamicin uptake in Staphylococcus aureus. , 1982, Proceedings of the National Academy of Sciences of the United States of America.

[15]  W. Epstein,et al.  Role of the membrane potential in bacterial resistance to aminoglycoside antibiotics , 1981, Antimicrobial Agents and Chemotherapy.

[16]  N. Hirota,et al.  Use of lipophilic cation-permeable mutants for measurement of transmembrane electrical potential in metabolizing cells of Escherichia coli , 1981, Journal of bacteriology.

[17]  E. R. Kashket Proton motive force in growing Streptococcus lactis and Staphylococcus aureus cells under aerobic and anaerobic conditions , 1981, Journal of bacteriology.

[18]  E. R. Kashket Effects of aerobiosis and nitrogen source on the proton motive force in growing Escherichia coli and Klebsiella pneumoniae cells , 1981, Journal of bacteriology.

[19]  Michael H. Miller,et al.  Gentamicin Uptake in Wild-Type and Aminoglycoside-Resistant Small-Colony Mutants of Staphylococcus aureus , 1980, Antimicrobial Agents and Chemotherapy.

[20]  C. Slayman,et al.  Quantitative measurements of membrane potential in Escherichia coli. , 1980, Biochemistry.

[21]  I. Friedberg,et al.  Electrochemical proton gradient in Micrococcus lysodeikticus cells and membrane vesicles , 1980, Journal of bacteriology.

[22]  R M Macnab,et al.  Proton chemical potential, proton electrical potential and bacterial motility. , 1980, Journal of molecular biology.

[23]  L. Leive,et al.  Two mutations which affect the barrier function of the Escherichia coli K-12 outer membrane , 1979, Journal of bacteriology.

[24]  S. Decker,et al.  Mutants of Bacillus megaterium resistant to uncouplers of oxidative phosphorylation. , 1977, The Journal of biological chemistry.

[25]  F. Harold,et al.  Circulation of H+ and K+ across the plasma membrane is not obligatory for bacterial growth. , 1977, Science.

[26]  E. Padan,et al.  The proton electrochemical gradient in Escherichia coli cells. , 1976, European journal of biochemistry.

[27]  J. S. Brand,et al.  Assay of picomole amounts of ATP, ADP, and AMP using the luciferase enzyme system. , 1975, Analytical biochemistry.

[28]  H. Winkler,et al.  Energy coupling for methionine transport in Escherichia coli , 1975, Journal of bacteriology.

[29]  P. Boyer,et al.  Energization of active transport by Escherichia coli. , 1972, The Journal of biological chemistry.

[30]  M. Harris,et al.  Effects of streptomycin in bacterial cultures growing at different rates; interaction with bacterial ribosomes in vivo. , 1969, European journal of biochemistry.

[31]  L. Leive,et al.  Release of lipopolysaccharide by EDTA treatment of E. coli. , 1965, Biochemical and biophysical research communications.

[32]  Oliver H. Lowry,et al.  Protein measurement with the Folin phenol reagent. , 1951, The Journal of biological chemistry.

[33]  A. Torriani-Gorini Phosphate metabolism and cellular regulation in microorganisms , 1987 .

[34]  V. Saunders,et al.  Accumulation of gentamicin by Staphylococcus aureus: the role of the transmembrane electrical potential. , 1986, The Journal of antimicrobial chemotherapy.

[35]  H. Rottenberg The measurement of membrane potential and deltapH in cells, organelles, and vesicles. , 1979, Methods in enzymology.

[36]  H. Kaback Transport across isolated bacterial cytoplasmic membranes. , 1972, Biochimica et biophysica acta.