Abstract

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 LPSS.minnesotaRe 595 (MW 2,500) and Lipid A fromS.minnesotaRe 595 (MW 2000) were 4 μM and 5 μM respectively. The CAC of LPS from heterogenous long O-antigen polysaccharide chain bacterial serotypes:S.minnesota wildtypewere 11 μg LPS/ml,S.typhimurium14 μg LPS/ml andE.coli0111:B4 22 μg LPS/ml, respectively. The result obtained suggests that critical aggregate concentration and solubility of LPS is a function of polysaccharide chain length.

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