Effect of Ce3+ on membrane permeability ofEscherichia coli cell

This study aimed to delineate the antibacterial mechanism of rare-earth ion Ce3+ to the target organism Escherichia coil cell, and the most important purpose was to identify its biological effect of increasing the E. coli cell membrane permeability. The antibacterial activi- ties of Ce3+ to E. coli...

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Published in中国稀土学报:英文版 Vol. 30; no. 9; pp. 947 - 951
Main Author CHEN Aimei SHI Qingshan OUYANG Yousheng CHEN Yiben
Format Journal Article
LanguageEnglish
Published 2012
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Abstract This study aimed to delineate the antibacterial mechanism of rare-earth ion Ce3+ to the target organism Escherichia coil cell, and the most important purpose was to identify its biological effect of increasing the E. coli cell membrane permeability. The antibacterial activi- ties of Ce3+ to E. coli cells were tested, and then the permeability of outer membrane (OM) and inner membrane (IM) were studied by N-phenyl-l-naphthylamine (NPN) and o-nitrophenyl-β-D-galactopyranoside (ONPG) methods separately. Through these experiments we concluded that the E. coli cells grown to log phage were more sensitive to Ce3+ than the ones not at this stage; the structure of membrane was destroyed and the permeability of both OM and IM was obviously increased by Ce3+; there should be certain interactions between Ce3+ and some proteins inside the cell, which impeded the physiological activities of bacteria.
AbstractList This study aimed to delineate the antibacterial mechanism of rare-earth ion Ce3+ to the target organism Escherichia coil cell, and the most important purpose was to identify its biological effect of increasing the E. coli cell membrane permeability. The antibacterial activi- ties of Ce3+ to E. coli cells were tested, and then the permeability of outer membrane (OM) and inner membrane (IM) were studied by N-phenyl-l-naphthylamine (NPN) and o-nitrophenyl-β-D-galactopyranoside (ONPG) methods separately. Through these experiments we concluded that the E. coli cells grown to log phage were more sensitive to Ce3+ than the ones not at this stage; the structure of membrane was destroyed and the permeability of both OM and IM was obviously increased by Ce3+; there should be certain interactions between Ce3+ and some proteins inside the cell, which impeded the physiological activities of bacteria.
Author CHEN Aimei SHI Qingshan OUYANG Yousheng CHEN Yiben
AuthorAffiliation Cruangdong Institute of Microbiology; Guangdong Open Laboratory of Applied Microbiology; Guangdong Province Key Laboratory of Microbial Culture Collection and Application, State Key Laboratory of Applied Microbiology (Ministry-Cruangdong Province Jointly Breeding Base), South China, Guangzhou 510070, China
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This study aimed to delineate the antibacterial mechanism of rare-earth ion Ce3+ to the target organism Escherichia coil cell, and the most important purpose was to identify its biological effect of increasing the E. coli cell membrane permeability. The antibacterial activi- ties of Ce3+ to E. coli cells were tested, and then the permeability of outer membrane (OM) and inner membrane (IM) were studied by N-phenyl-l-naphthylamine (NPN) and o-nitrophenyl-β-D-galactopyranoside (ONPG) methods separately. Through these experiments we concluded that the E. coli cells grown to log phage were more sensitive to Ce3+ than the ones not at this stage; the structure of membrane was destroyed and the permeability of both OM and IM was obviously increased by Ce3+; there should be certain interactions between Ce3+ and some proteins inside the cell, which impeded the physiological activities of bacteria.
cerium ion; antibacterial activity; outer membrane; inner membrane; membrane permeability; rare earths
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PublicationTitle 中国稀土学报:英文版
PublicationTitleAlternate Journal of Rare Earths
PublicationYear 2012
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Snippet This study aimed to delineate the antibacterial mechanism of rare-earth ion Ce3+ to the target organism Escherichia coil cell, and the most important purpose...
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SubjectTerms 半乳糖苷
大肠杆菌细胞
抗菌机理
活性关系
生物学效应
硝基苯基
稀土离子
膜通透性
Title Effect of Ce3+ on membrane permeability ofEscherichia coli cell
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