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Structural analysis of lipid A from Escherichia coli O157:H7:K − using thin‐layer chromatography and ion‐trap mass spectrometry
Author(s) -
Lee ChangSoo,
Kim YunGon,
Joo HwangSoo,
Kim ByungGee
Publication year - 2004
Publication title -
journal of mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.475
H-Index - 121
eISSN - 1096-9888
pISSN - 1076-5174
DOI - 10.1002/jms.614
Subject(s) - chemistry , mass spectrometry , thin layer chromatography , ion , chromatography , thin layer , escherichia coli , trap (plumbing) , ion trap , layer (electronics) , ion chromatography , analytical chemistry (journal) , organic chemistry , biochemistry , environmental engineering , engineering , gene
Rapid separation and structural identification of lipid A from Escherichia coli were performed using thin‐layer chromatography (TLC) and mass spectrometry (MS). After the resolved spot of the lipid A had been scraped from TLC plate, the sample was re‐extracted from the removed powder with chloroform–methanol (2 : 1, v/v) and analyzed by matrix‐assisted laser desorption/ionization time‐of‐flight (MALDI‐TOF) and electrospray ionization (ESI) ion‐trap MS. For detailed structural characterization, multiple‐stage mass analysis (MS 4 ) of the major species in ESI‐MS/MS provided important information about the series of fragment ions. The dominant fragment ions in each MS stage were produced from the loss of fatty acyl groups mainly driven by charge‐remote processes, and this information about the fragment ions can be used to deduce the composition or the position of the fatty acid substituent in the lipid A. In contrast, MALDI‐TOFMS indicated that fragmentation resulted from charge‐driven processes. Molecular mass profiling and fragmentation analysis provides essential information for clarifying the detailed structure of the lipid A from E. coli O157:H7:K − . Copyright © 2004 John Wiley & Sons, Ltd.