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肺炎克雷伯菌O3脂多糖的佐剂活性:蛋白质对佐剂活性表达无贡献。

Adjuvant activity of Klebsiella O3 lipopolysaccharide: no contribution of proteins to the expression of adjuvant activity.

作者信息

Kato N, Kido N, Ohta M, Naito S, Hasegawa T, Mori M, Agata N, Nakashima I, Kuno T

出版信息

Microbiol Immunol. 1983;27(12):1043-55. doi: 10.1111/j.1348-0421.1983.tb02938.x.

Abstract

Previously we found that Klebsiella O3 lipopolysaccharide (KO3 LPS) isolated from culture supernatant of strain Kasuya (O3: K1) or its decapsulated mutant strain LEN-1 (O3: K1-) exhibited very strong adjuvant activity in augmenting antibody response and delayed-type hypersensitivity to protein antigens in mice. The preparation of KO3 LPS after deproteinization by four cycles of treatment with chloroform-butanol (5: 1) usually contained a small percentage of proteins and a definite amount of another antigen which was destroyed by heating at 100 C for 1 hr. This antigen proved to be derived from type 1 fimbriae which are responsible for mannose-sensitive hemagglutination of guinea pig erythrocytes. The preparation of KO3 LPS isolated from culture supernatant of the strains which did not produce type 1 fimbriae exhibited strong adjuvant activity similar to that of the preparation from those which produced them. The preparation of KO3 LPS treated with hot phenol water which is known to remove lipid A-associated proteins exhibited a similar strong adjuvant activity. The preparation of KO3 LPS after extensive deproteinizing, two cycles of pronase treatment followed by ten cycles of treatment with chloroform-butanol, no longer contained detectable amounts of proteins and the fimbrial antigen, but this preparation also exhibited similar strong adjuvant activity. Moreover, there was no difference in strength of the adjuvant activity between the preparation of KO3 LPS isolated from culture supernatant and that isolated by the phenol method from bacterial cells. The present study demonstrates that the strong adjuvant activity of the preparation of KO3 LPS does not depend in any way on proteins contaminating the preparation.

摘要

先前我们发现,从春日株(O3:K1)或其去荚膜突变株LEN-1(O3:K1-)的培养上清液中分离出的肺炎克雷伯菌O3脂多糖(KO3 LPS),在增强小鼠对蛋白质抗原的抗体反应和迟发型超敏反应方面表现出非常强的佐剂活性。用氯仿-丁醇(5:1)处理四个循环进行脱蛋白后制备的KO3 LPS通常含有少量蛋白质和一定量的另一种抗原,该抗原在100℃加热1小时后被破坏。事实证明,这种抗原来自1型菌毛,它负责豚鼠红细胞的甘露糖敏感血凝反应。从不产生1型菌毛的菌株的培养上清液中分离出的KO3 LPS制剂表现出与从产生1型菌毛的菌株中分离出的制剂相似的强佐剂活性。用已知可去除与脂多糖A相关蛋白质的热酚水进行处理的KO3 LPS制剂也表现出类似的强佐剂活性。经过广泛脱蛋白处理(先用链霉蛋白酶处理两个循环,然后用氯仿-丁醇处理十个循环)的KO3 LPS制剂不再含有可检测到的蛋白质和菌毛抗原,但该制剂也表现出类似的强佐剂活性。此外,从培养上清液中分离出的KO3 LPS制剂与用苯酚法从细菌细胞中分离出的制剂之间的佐剂活性强度没有差异。本研究表明,KO3 LPS制剂的强佐剂活性绝不依赖于制剂中污染的蛋白质。

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