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用简单多糖制备鲎试剂明胶。

Gelatin of Limulus amoebocyte lysate by simple polysaccharides.

作者信息

Mikami T, Nagase T, Suzuki S, Suzuki M

出版信息

Microbiol Immunol. 1982;26(5):403-9. doi: 10.1111/j.1348-0421.1982.tb00190.x.

DOI:10.1111/j.1348-0421.1982.tb00190.x
PMID:6181382
Abstract

The Limulus lysate gelatin activity of several simple polysaccharides including yeast mannans and bacterial dextrans was investigated. The mannans from Saccharomyces cerevisiae wild and mutant strains possessing dense branches showed positive gelatin activity at concentrations of 1 microgram/ml or more regardless of differences in their chemical structure. However, two synthetic mannans possessing linear structures with alpha 1 leads to 2 and alpha 1 leads to 6 linkages also gave positive reactions at concentrations of 10 microgram/ml or more and 500 microgram/ml or more, respectively. The dextran from Leuconostoc mesenteroides IAM 1046 consisting of a dense branching moiety displayed reactivity at concentrations of 100 microgram/ml or more, while the dextrans devoid of such branches were negative in this reaction. The optimal concentration for Limulus lysate gelatin could not be determined for any of the polysaccharides and lipopolysaccharides (LPS) tested in this study. The gelation activity of the polysaccharides was stable to treatment with 100 mM NaOH at 30 C for 72 hr. The minimum concentration for the gelation activity of LPS treated with 100 mM NaOH under the same conditions was reduced from 10(-6) approximately(-9) microgram/ml to 1-10 microgram/ml. The above findings demonstrate that the major part of Limulus lysate gelation activity of LPS depends on the alkali-degradable lipid A moiety, and that such simple polysaccharides are also able to participate in this activity even though the extent of participation is very low.

摘要

研究了几种简单多糖(包括酵母甘露聚糖和细菌葡聚糖)的鲎试剂明胶活性。来自具有密集分支的酿酒酵母野生型和突变株的甘露聚糖,无论其化学结构有何差异,在浓度为1微克/毫升或更高时均表现出阳性明胶活性。然而,两种具有α1→2和α1→6连接的线性结构的合成甘露聚糖,分别在浓度为10微克/毫升或更高和500微克/毫升或更高时也给出阳性反应。来自肠膜明串珠菌IAM 1046的具有密集分支部分的葡聚糖在浓度为100微克/毫升或更高时显示出反应性,而没有这种分支的葡聚糖在该反应中为阴性。在本研究中测试的任何多糖和脂多糖(LPS)都无法确定鲎试剂明胶的最佳浓度。多糖的凝胶化活性在30℃下用100 mM NaOH处理72小时后是稳定的。在相同条件下用100 mM NaOH处理的LPS的凝胶化活性的最低浓度从10^(-6)~10^(-9)微克/毫升降低到1~10微克/毫升。上述发现表明,LPS的鲎试剂凝胶化活性的主要部分取决于碱可降解的脂质A部分,并且即使参与程度非常低,这些简单多糖也能够参与该活性。

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