Synergistic effect of lactate and Fe2+ on cell killing in E. coli and other bacteria

K. Ohshiro, J. Ueno, M. Aktar Ali, N. Murakami, T. Konishi

Research output: Contribution to journalArticle

Abstract

Since we previously found that lactate enhances OH radical generation in the Fenton reaction, the bactericidal effect of lactate modified Fenton reaction was studied on E. coli JM109 by the colony counting method. However, the lactate addition did not significantly enhance the cytotoxicity of pure Fenton system. The colony forming ability of E. coli was seriously damaged by lactate/Fe2+ coupled without H2O2. The viable cell number decreased with increasing concentrations of lactate in the presence of a fixed amount of Fe2+. Likewise, Fe2+ cytotoxicity was markedly enhanced in the presence of lactate, although Fe3+ was essentially non-toxic up to 1 mM in spite of lactate presence. Since Fe2+ chelating agent, deferoxamine inhibited the lethal effect of lactate/Fe2+ couple, an increased cellular uptake of Fe2+ was expected to be the cause of cytotoxicity induced by the lactate/Fe2+ couple. However, the cytotoxicity was not manipulated in the presence of membrane permeable OH radical scavengers, indicating intracellular Fenton reaction mediated by the Fe2+ may not be the only cause of cell death. The lethal effect of lactate/Fe2+ couple was also observed in other bacterial strains such as Bacillus subtilis ATCC 6633, Pseudomonas aeruginosa ATCC 27853 and Klebsiella pneumoniae ATCC 13883. No relationship was determined between their gram staining natures and the sensitivities toward lactate/Fe2+.

Original languageEnglish (US)
Pages (from-to)215-222
Number of pages8
JournalResearch Communications in Biochemistry and Cell and Molecular Biology
Volume3
Issue number3-4
StatePublished - 1999

Fingerprint

Escherichia coli
Lactic Acid
Bacteria
Cells
Cytotoxicity
Deferoxamine
Klebsiella pneumoniae
Bacilli
Cell death
Chelating Agents
Bacillus subtilis
Pseudomonas aeruginosa
Cause of Death
Cell Death
Cell Count
Staining and Labeling
Membranes

ASJC Scopus subject areas

  • Cell Biology
  • Clinical Biochemistry
  • Molecular Biology

Cite this

Synergistic effect of lactate and Fe2+ on cell killing in E. coli and other bacteria. / Ohshiro, K.; Ueno, J.; Aktar Ali, M.; Murakami, N.; Konishi, T.

In: Research Communications in Biochemistry and Cell and Molecular Biology, Vol. 3, No. 3-4, 1999, p. 215-222.

Research output: Contribution to journalArticle

Ohshiro, K. ; Ueno, J. ; Aktar Ali, M. ; Murakami, N. ; Konishi, T. / Synergistic effect of lactate and Fe2+ on cell killing in E. coli and other bacteria. In: Research Communications in Biochemistry and Cell and Molecular Biology. 1999 ; Vol. 3, No. 3-4. pp. 215-222.
@article{90fec3ce81764e03b35f31272d442eb9,
title = "Synergistic effect of lactate and Fe2+ on cell killing in E. coli and other bacteria",
abstract = "Since we previously found that lactate enhances OH radical generation in the Fenton reaction, the bactericidal effect of lactate modified Fenton reaction was studied on E. coli JM109 by the colony counting method. However, the lactate addition did not significantly enhance the cytotoxicity of pure Fenton system. The colony forming ability of E. coli was seriously damaged by lactate/Fe2+ coupled without H2O2. The viable cell number decreased with increasing concentrations of lactate in the presence of a fixed amount of Fe2+. Likewise, Fe2+ cytotoxicity was markedly enhanced in the presence of lactate, although Fe3+ was essentially non-toxic up to 1 mM in spite of lactate presence. Since Fe2+ chelating agent, deferoxamine inhibited the lethal effect of lactate/Fe2+ couple, an increased cellular uptake of Fe2+ was expected to be the cause of cytotoxicity induced by the lactate/Fe2+ couple. However, the cytotoxicity was not manipulated in the presence of membrane permeable OH radical scavengers, indicating intracellular Fenton reaction mediated by the Fe2+ may not be the only cause of cell death. The lethal effect of lactate/Fe2+ couple was also observed in other bacterial strains such as Bacillus subtilis ATCC 6633, Pseudomonas aeruginosa ATCC 27853 and Klebsiella pneumoniae ATCC 13883. No relationship was determined between their gram staining natures and the sensitivities toward lactate/Fe2+.",
author = "K. Ohshiro and J. Ueno and {Aktar Ali}, M. and N. Murakami and T. Konishi",
year = "1999",
language = "English (US)",
volume = "3",
pages = "215--222",
journal = "Research Communications in Biochemistry and Cell and Molecular Biology",
issn = "1087-111X",
publisher = "PJD Publications Ltd",
number = "3-4",

}

TY - JOUR

T1 - Synergistic effect of lactate and Fe2+ on cell killing in E. coli and other bacteria

AU - Ohshiro, K.

AU - Ueno, J.

AU - Aktar Ali, M.

AU - Murakami, N.

AU - Konishi, T.

PY - 1999

Y1 - 1999

N2 - Since we previously found that lactate enhances OH radical generation in the Fenton reaction, the bactericidal effect of lactate modified Fenton reaction was studied on E. coli JM109 by the colony counting method. However, the lactate addition did not significantly enhance the cytotoxicity of pure Fenton system. The colony forming ability of E. coli was seriously damaged by lactate/Fe2+ coupled without H2O2. The viable cell number decreased with increasing concentrations of lactate in the presence of a fixed amount of Fe2+. Likewise, Fe2+ cytotoxicity was markedly enhanced in the presence of lactate, although Fe3+ was essentially non-toxic up to 1 mM in spite of lactate presence. Since Fe2+ chelating agent, deferoxamine inhibited the lethal effect of lactate/Fe2+ couple, an increased cellular uptake of Fe2+ was expected to be the cause of cytotoxicity induced by the lactate/Fe2+ couple. However, the cytotoxicity was not manipulated in the presence of membrane permeable OH radical scavengers, indicating intracellular Fenton reaction mediated by the Fe2+ may not be the only cause of cell death. The lethal effect of lactate/Fe2+ couple was also observed in other bacterial strains such as Bacillus subtilis ATCC 6633, Pseudomonas aeruginosa ATCC 27853 and Klebsiella pneumoniae ATCC 13883. No relationship was determined between their gram staining natures and the sensitivities toward lactate/Fe2+.

AB - Since we previously found that lactate enhances OH radical generation in the Fenton reaction, the bactericidal effect of lactate modified Fenton reaction was studied on E. coli JM109 by the colony counting method. However, the lactate addition did not significantly enhance the cytotoxicity of pure Fenton system. The colony forming ability of E. coli was seriously damaged by lactate/Fe2+ coupled without H2O2. The viable cell number decreased with increasing concentrations of lactate in the presence of a fixed amount of Fe2+. Likewise, Fe2+ cytotoxicity was markedly enhanced in the presence of lactate, although Fe3+ was essentially non-toxic up to 1 mM in spite of lactate presence. Since Fe2+ chelating agent, deferoxamine inhibited the lethal effect of lactate/Fe2+ couple, an increased cellular uptake of Fe2+ was expected to be the cause of cytotoxicity induced by the lactate/Fe2+ couple. However, the cytotoxicity was not manipulated in the presence of membrane permeable OH radical scavengers, indicating intracellular Fenton reaction mediated by the Fe2+ may not be the only cause of cell death. The lethal effect of lactate/Fe2+ couple was also observed in other bacterial strains such as Bacillus subtilis ATCC 6633, Pseudomonas aeruginosa ATCC 27853 and Klebsiella pneumoniae ATCC 13883. No relationship was determined between their gram staining natures and the sensitivities toward lactate/Fe2+.

UR - http://www.scopus.com/inward/record.url?scp=0033502144&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0033502144&partnerID=8YFLogxK

M3 - Article

AN - SCOPUS:0033502144

VL - 3

SP - 215

EP - 222

JO - Research Communications in Biochemistry and Cell and Molecular Biology

JF - Research Communications in Biochemistry and Cell and Molecular Biology

SN - 1087-111X

IS - 3-4

ER -