Dual antibacterial mechanisms of nisin Z against Gram-positive and Gram-negative bacteria

被引:136
作者
Kuwano, K
Tanaka, N
Shimizu, T
Nagatoshi, K
Nou, S
Sonomoto, K
机构
[1] Kurume Univ, Sch Med, Dept Bacteriol, Fukuoka 8300011, Japan
[2] Omu Milk Prod Co Ltd, Div Res & Dev, Fukuoka 8360895, Japan
[3] Kyushu Univ, Grad Sch, Fac Agr, Dept Biosci & Biotechnol, Fukuoka 8128581, Japan
关键词
nisin Z; cationic peptide; antibacterial activity; membrane permeabilisation; vancomycin; lipid II;
D O I
10.1016/j.ijantimicag.2005.08.010
中图分类号
R51 [传染病];
学科分类号
100401 [流行病与卫生统计学];
摘要
Nisin, an amphipathic antibiotic peptide, is produced by a number of strains of Lactococcus lactis subsp. lactis. It has been employed as a food preservative as it has a high antibacterial activity with a relatively low toxicity for humans. Nisin is known to exert a high antibacterial activity against Gram-positive but not Gram-negative bacteria. However, purified nisin Z was found to show an antibacterial activity both against Gram-positive and Gram-negative bacteria. To clarify the mechanisms of activity, nisin Z and purified nisin Z were tested for their antibacterial activities in a high-salt environment. The activity of nisin Z against Staphylococcus aureus was stable even in the presence of NaCl at 100 mM, showing ca. 2 log colony-forming unit (CFU) reduction. In contrast, the activity of nisin Z against Escherichia coli was highly sensitive to the same concentration of NaCl, and CFU reduction was not observed. Furthermore, purified nisin Z caused the permeabilisation both of S. aureus and E. coli cytoplasmic membranes. The permeabilisation of E. coli but not S. aureus cytoplasmic membranes was remarkably reduced in a high-salt environment. Moreover, vancomycin inhibited the nisin Z-induced permeabilisation of the S. aureus cytoplasmic membrane. These results suggest that nisin Z utilises two distinct mechanisms of antibacterial activity: a high-salt-sensitive mechanism for E. coli and a high-salt-insensitive mechanism for S. aureus. (C) 2005 Elsevier B.V. and the International Society of Chemotherapy. All rights reserved.
引用
收藏
页码:396 / 402
页数:7
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