Isolation and characterization of lipopolysaccharide from Centipeda periodontii ATCC 35019

Oral Microbiol Immunol. 1990 Apr;5(2):108-12. doi: 10.1111/j.1399-302x.1990.tb00237.x.

Abstract

Lipopolysaccharide (LPS) was extracted from cells of Centipeda periodontii ATCC 35019 by a hot phenol-water method, purified by nuclease treatment and by repeated ultracentrifugations. The LPS was composed of 21.7% hexose, 9.1% hexosamine, 10.3% fatty acid, 0.5% protein, 2.5% phosphorus, 4.3% 2-keto-3-deoxyoctonate(KDO) and 2.3% heptose. The major fatty acids of the LPS were 3OH C13:0 and C13:0. C. periodontii LPS was able to gelatinize Limulus amebocyte and to produce the local Schwartzman reaction in rabbits. LPS from C. periodontii exhibited strong immunobiological activities, mitogenicity on splenocytes of C3H/HeN mice, and stimulation of interleukin 1 (IL-1) production in peritoneal macrophages of C3H/HeN mice.

MeSH terms

  • Endotoxins
  • Fatty Acids
  • Gram-Negative Anaerobic Bacteria*
  • Humans
  • Interleukin-1 / biosynthesis
  • Limulus Test
  • Lipopolysaccharides / chemistry
  • Lipopolysaccharides / isolation & purification*
  • Mitogens
  • Periodontitis / microbiology
  • Phenols
  • Polysaccharides, Bacterial / chemistry
  • Polysaccharides, Bacterial / isolation & purification

Substances

  • Endotoxins
  • Fatty Acids
  • Interleukin-1
  • Lipopolysaccharides
  • Mitogens
  • Phenols
  • Polysaccharides, Bacterial