4.6 Article

Multi-spectrometric analyses of lipoteichoic acids isolated from Lactobacillus plantarum

Journal

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbrc.2011.03.107

Keywords

Lipoteichoic acid; Lactobacillus plantarum; Anti-inflammatory; NMR; MALDI-TOF/TOF

Funding

  1. Korea Biotech RD Group of Next-generation of Next-generation growth engine Project [F104AD010001-08A0401-00130]
  2. 21C Frontier Microbial Genomics and Applications Center [M102KK010016-08K1101-01650]
  3. Ministry of Education, Science and Technology (MEST), Republic of Korea [R322009000102130]
  4. National Research Foundation of Korea [2007-0055756, 2006-2008395] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Lipoteichoic acid is a major cell wall virulence factor of gram-positive bacteria. LTAs from various bacteria have differential immunostimulatory potentials due to heterogeneity in their structures. Although recent studies have demonstrated that LTA isolated from Lactobacillus plantarum (pLTA) has anti-inflammatory properties and is less inflammatory than LTAs from pathogenic bacteria, little is known about the structure of pLTA. In this study, high-field NMR spectra of the pLTA were compared with those of LTA from pathogenic bacterium, Staphylococcus aureus (aLTA). The 2D NMR results demonstrated that pLTA possesses alpha-linked hexose sugar substituents on the poly-glycerophosphate backbone instead of N-acetyl-glucosamine substituents, and unsaturated fatty acids in its glycolipids. The sugar substituents were revealed as an approximately 29:1 molar ratio of the glucose to galactose by HPAEC-PAD analysis. MALDI-TOF/TOF MS analyses identified the presence of unsaturated fatty acids in the glycolipid moieties of pLTA. In addition, the glycolipid structure was found to be composed of trihexosyl-diacyl- and/or trihexosyl-triacyl-glycerol ceramide units by means of unique fragment ions of the glycolipids. These results enabled us to elucidate the pLTA structure, which is distinctively different from canonical LTA structure, and suggest that the unique immunological property of pLTA might be caused by the pLTA structure. (C) 2011 Elsevier Inc. All rights reserved.

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