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[来自青枯雷尔氏菌ICMP 7859的脂多糖及其修饰衍生物的生物活性]

[The biological activity of a lipopolysaccharide from Ralstonia solanacearum ICMP 7859 and of its modified derivative].

作者信息

Varbanets L D, Seĭfullina I I, Rybalko S L, Diadiun S T, Brovarskaia O S

机构信息

Institute of Microbiology and Virology, National Academy of Sciences of Ukraine, Kyiv.

出版信息

Mikrobiol Z. 1998 Jul-Aug;60(4):80-7.

PMID:9859644
Abstract

Coordinational compound of the Ralstonia solanacearum ICMP 7859 lipopolysaccharide (LPS) with germanium was obtained. The derivative has lost to considerable extent its toxicity (as compared to the initial substance) but preserves immunomodulating activity, interferon-inducing one in particular. Lipid A modification has led to complete loss of interferon-inducing activity. Apparently, phosphate at C4' GlcN II can be responsible for interferon-inducing activity of lipid A, while carboxylic groups of core oligosaccharide or 0-specific polysaccharide, are responsible for that in native molecule of LPS.

摘要

获得了青枯雷尔氏菌ICMP 7859脂多糖(LPS)与锗的配位化合物。该衍生物在很大程度上丧失了其毒性(与初始物质相比),但保留了免疫调节活性,尤其是干扰素诱导活性。脂质A修饰导致干扰素诱导活性完全丧失。显然,C4' GlcN II上的磷酸可能是脂质A干扰素诱导活性的原因,而核心寡糖或O-特异性多糖的羧基则是LPS天然分子中该活性的原因。

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