Bacterial membrane injuries induced by lactacin F and nisin

被引:17
作者
Dalmau M. [1 ]
Maier E. [2 ]
Mulet N. [1 ]
Viñas M. [1 ]
Benz R. [2 ]
机构
[1] Biomedical Research Center of Bellvitge, Laboratory of Microbiology, University of Barcelona
[2] Lehrstuhl für Biotechnologie, Theodor-Boveri-Institut (Biozentrum), Universität Würzburg, 97074 Würzburg, Am Hubland
关键词
Flow cytometry; Lactacin F; Lactic acid bacteria (LAB); Nisin; Planar lipid bilayer;
D O I
10.1007/s10123-002-0063-2
中图分类号
学科分类号
摘要
The combined action of nisin and lactacin F, two bacteriocins produced by lactic acid bacteria, is additive. In this report, the basis of this effect is examined. Channels formed by lactacin F were studied by experiments using planar lipid bilayers, and bactericidal effects were analyzed by flow cytometry. Lactacin F produced pores with a conductance of 1 ns in black lipid bilayers in 1 mM KCl at 10 mV at 20 °C. Pore formation was strongly dependent on voltage. Although lactacin F formed pores at very low potential (10 mV), the dependence was exponential above 40 mV. The injuries induced by nisin and lactacin F in the membranes of Lactobacillus helveticus produced different flow cytometric profiles. Probably, when both bacteriocins are present, each acts separately; their cooperation may be due to an increase in the number of single membrane injuries. © Springer-Verlag and SEM 2002.
引用
收藏
页码:73 / 80
页数:7
相关论文
共 34 条
[1]  
Abee T., Klaenhammer T.R., Letellier L., Kinetic studies of the action of lactacin F, a bacteriocin produced by Lactobacillus johnsonii that forms poration complexes in the cytoplasmic membrane, Appl Environ Microbiol, 60, pp. 1006-1013, (1994)
[2]  
Allison G.E., Fremaux C., Klaenhammer T.R., Expansion of bacteriocin activity and host range upon complementation of two peptides encoded within the lactacin F operon, J Bacteriol, 176, pp. 2235-2241, (1994)
[3]  
Allison G.E., Worobo R.W., Stiles M.E., Klaenhammer T.R., Heterologous expression of the lactacin F peptides by Carnobacterium piscicola LV17, Appl Environ Microbiol, 61, pp. 1371-1377, (1995)
[4]  
Alvarez-Barrientos A., Arroyo J., Canton R., Nombela C., Sanchez-Perez M., Applications of flow cytometry to clinical Microbiology, Clin Microbiol Rev, 13, pp. 167-195, (2000)
[5]  
Arana I., Pocino M., Muela A., Fernandez-Astorga A., Barcina I., Detection and enumeration of viable but non-culturable transconjugants of Escherichia coli during the survival of recipient cells in river water, J Appl Microbiol, 83, pp. 340-346, (1997)
[6]  
Barcina I., Survival strategies of enteric bacteria in aquatic systems, Microbiologia SEM, 11, pp. 389-392, (1995)
[7]  
Benz R., Janko K., Boos W., Lauger P., Formation of large, ion-permeable membrane channels by the matrix protein (porin) of Escherichia coli, Biochim Biophys Acta, 511, pp. 305-319, (1978)
[8]  
Benz R., Janko K., Lauger P., Ionic selectivity of pores formed by the matrix protein (porin) of Escherichia coli, Biochim Biophys Acta, 551, pp. 238-247, (1979)
[9]  
Benz R., Jung G., Sahl H.G., Mechanism of channel-formation by lantibiotics in black lipid membranes, Nisin and Novel Lantibiotics, pp. 359-372, (1991)
[10]  
Benz R., Solute uptake through bacterial outer membranes, Bacterial Cell Wall, pp. 397-423, (1994)