Isolation, Purification, Characterization and Direct Conjugation of the Lipid A-Free Lipopolysaccharide of Vibrio cholerae O139.
Peng XuJana KorcováPeter BaráthAlžbeta ČížováJana ValárikováFirdausi QadriMeagan KellyRobert D O'ConnorEdward T RyanSlavomír BystrickýPavol KováčPublished in: Chemistry (Weinheim an der Bergstrasse, Germany) (2019)
The lipopolysaccharide (LPS) of Vibrio cholerae O139, strain CIRS245, was isolated conventionally, and the lipid A was removed by mild acid hydrolysis (0.1 m NaOAc buffer containing 1 % SDS, pH 4.2, 95 °C, 8 h). The crude product was a complex mixture consisting mainly of constituent fragments of the O-specific polysaccharide-core (OSPc). The OSPc was only a minor component in the mixture. Two-stage purification of the crude OSPc by HPLC gave pure OSPc fragment of the LPS, as shown by NMR spectroscopy, analytical HPLC and ESI-MS. This material is the purest OSPc fragment of the LPS from Vibrio cholerae O139 reported to date. The purified OSPc was readily converted to the corresponding methyl squarate derivative and the latter was conjugated to BSA. The conjugate, when examined by ELISA, showed immunoreactivity with sera from patients in Bangladesh recovering from cholera caused by V. cholerae O139, but not O1.
Keyphrases
- ms ms
- inflammatory response
- end stage renal disease
- lps induced
- mass spectrometry
- anti inflammatory
- toll like receptor
- simultaneous determination
- chronic kidney disease
- ejection fraction
- newly diagnosed
- high performance liquid chromatography
- multiple sclerosis
- peritoneal dialysis
- fatty acid
- prognostic factors
- solid phase extraction
- liquid chromatography
- tandem mass spectrometry
- cancer therapy
- immune response
- high resolution
- water soluble
- monoclonal antibody