Efficient method for preparation of highly purified lipopolysaccharides by hydrophobic interaction chromatography

被引:15
|
作者
Muck, A [1 ]
Ramm, M [1 ]
Hamburger, M [1 ]
机构
[1] Univ Jena, Inst Pharm, Lehrstuhl Pharmazeut Biol, D-07743 Jena, Germany
来源
JOURNAL OF CHROMATOGRAPHY B | 1999年 / 732卷 / 01期
关键词
cell wall composition; lipopolysaccharides;
D O I
10.1016/S0378-4347(99)00256-X
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A method for the efficient preparation of highly purified lipopolysaccharides (LPSs) by hydrophobic interaction chromatography (HIC) has been developed. The procedure can be used for the purification of cell wall bound LPSs after hot phenol-water extraction and for the isolation of extracellular LPSs from the supernatant, respectively. The method described has been tested with artificial mixtures containing LPSs, polysaccharide, protein and RNA and subsequently employed for the preparative purification of two LPSs of different origin, namely the extracellular LPS secreted by Escherichia coli E49 into the culture medium, and the cell wall bound LPS from Pseudomonas aeruginosa VA11465/1. Compared to currently used methods for LPS purification such as enzymatic digestion and ultracentrifugation, the chromatographic separation reported here combines superior purity with minimal loss of LPS, high reproducibility and simple handling. The removal of contaminants such as protein, RNA and polysaccharides and the recovery of LPSs were monitored by appropriate assays. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:39 / 46
页数:8
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