Aurell C A, Wistrom A O
Department of Chemical and Environmental Engineering, University of California, Riverside 92521, USA.
Biochem Biophys Res Commun. 1998 Dec 9;253(1):119-23. doi: 10.1006/bbrc.1998.9773.
Bacterial endotoxins or lipopolysaccharides (LPS), cell wall components of gram negative bacteria, are involved in septic shock. While the carbohydrate structure of LPS have been studied in the past, little is known about the macromolecular structure and formation of LPS fragments in blood. It is believed that amphiphilic molecules such as LPS occur as monomers and aggregate into macromolecular structures above a critical micelle or critical aggregate concentration, CAC. The CAC of Lipid A, a LPS precursor, and several LPS serotypes of varying molecular weight and different polysaccharide chain lengths were established by static light scattering and by steady-state fluorescence spectroscopy by incorporation of the fluorescent probe, NPN, N-phenyl-1-naphthylamine. The CAC for short polysaccharide chain mutant LPS S.minnesota Re 595 (MW 2,500) and Lipid A from S.minnesota Re 595 (MW 2000) were 4 microM and 5 microM respectively. The CAC of LPS from heterogeneous long O-antigen polysaccharide chain bacterial serotypes: S.minnesota wildtype were 11 micrograms LPS/ml, S.typhimurium 14 micrograms LPS/ml and E.coli 0111:B4 22 micrograms LPS/ml, respectively. The results obtained suggests that critical aggregate concentration and solubility of LPS is a function of polysaccharide chain length.
细菌内毒素或脂多糖(LPS)是革兰氏阴性菌的细胞壁成分,与脓毒症休克有关。虽然过去已经对LPS的碳水化合物结构进行了研究,但对于血液中LPS片段的大分子结构和形成却知之甚少。据信,诸如LPS之类的两亲性分子以单体形式存在,并在高于临界胶束浓度或临界聚集浓度(CAC)时聚集形成大分子结构。通过静态光散射以及通过掺入荧光探针NPN(N-苯基-1-萘胺)的稳态荧光光谱法,确定了LPS前体脂质A以及几种不同分子量和不同多糖链长度的LPS血清型的CAC。短多糖链突变体LPS S.minnesota Re 595(分子量2500)和来自S.minnesota Re 595的脂质A(分子量2000)的CAC分别为4 microM和5 microM。来自具有不同长O抗原多糖链细菌血清型的LPS的CAC:S.minnesota野生型分别为11微克LPS/毫升,鼠伤寒沙门氏菌为14微克LPS/毫升,大肠杆菌0111:B4为22微克LPS/毫升。所获得的结果表明,LPS的临界聚集浓度和溶解度是多糖链长度的函数。