TY - JOUR
T1 - Structural analysis of the lipid A isolated from Hafnia alvei 32 and PCM 1192 lipopolysaccharides
AU - Lukasiewicz, Jolanta
AU - Jachymek, Wojciech
AU - Niedziela, Tomasz
AU - Kenne, Lennart
AU - Lugowski, Czeslaw
PY - 2010
Y1 - 2010
N2 - Hafnia alvei, a Gram-negative bacterium, is an opportunistic pathogen associated with mixed hospital infections, bacteremia, septicemia, and respiratory diseases. The majority of clinical symptoms of diseases caused by this bacterium have a lipopolysaccharide (LPS, endotoxin)-related origin. The lipid A structure affects the biological activity of endotoxins predominantly. Thus, the structure of H. alvei lipid A was analyzed for the first time. The major form, asymmetrically hexa-acylated lipid A built of beta-D-GlcpN4P-(1 -> 6)-alpha-D-GlcpN1P substituted with (R)-14:0(3-OH) at N-2 and O-3, 14:0(3-(R)-O-12:0) at N-2', and 14:0(3-(R)-O-14:0) at O-3', was identified by ESI-MS(n) and MALDI-time-of-flight (TOF) MS. Comparative analysis performed by MS suggested that LPSs of H. alvei 32, PCM 1192, PCM 1206, and PCM 1207 share the identified structure of lipid A. LPSs of H. alvei are yet another example of enterobacterial endotoxins having the Escherichia coli-type structure of lipid A. The presence of hepta-acylated forms of H. alvei lipid A resulted from the addition of palmitate (16:0) substituting 14:0(3-OH) at N-2 of the alpha-GlcpN residue. All the studied strains of H. alvei have an ability to modify their lipid A structure by palmitoylation.-Lukasiewicz, J., W. Jachymek, T. Niedziela, L. Kenne, and C. Lugowski. Structural analysis of the lipid A isolated from Hafnia alvei 32 and PCM 1192 lipopolysaccharides. J. Lipid Res. 2010. 51: 564-574.
AB - Hafnia alvei, a Gram-negative bacterium, is an opportunistic pathogen associated with mixed hospital infections, bacteremia, septicemia, and respiratory diseases. The majority of clinical symptoms of diseases caused by this bacterium have a lipopolysaccharide (LPS, endotoxin)-related origin. The lipid A structure affects the biological activity of endotoxins predominantly. Thus, the structure of H. alvei lipid A was analyzed for the first time. The major form, asymmetrically hexa-acylated lipid A built of beta-D-GlcpN4P-(1 -> 6)-alpha-D-GlcpN1P substituted with (R)-14:0(3-OH) at N-2 and O-3, 14:0(3-(R)-O-12:0) at N-2', and 14:0(3-(R)-O-14:0) at O-3', was identified by ESI-MS(n) and MALDI-time-of-flight (TOF) MS. Comparative analysis performed by MS suggested that LPSs of H. alvei 32, PCM 1192, PCM 1206, and PCM 1207 share the identified structure of lipid A. LPSs of H. alvei are yet another example of enterobacterial endotoxins having the Escherichia coli-type structure of lipid A. The presence of hepta-acylated forms of H. alvei lipid A resulted from the addition of palmitate (16:0) substituting 14:0(3-OH) at N-2 of the alpha-GlcpN residue. All the studied strains of H. alvei have an ability to modify their lipid A structure by palmitoylation.-Lukasiewicz, J., W. Jachymek, T. Niedziela, L. Kenne, and C. Lugowski. Structural analysis of the lipid A isolated from Hafnia alvei 32 and PCM 1192 lipopolysaccharides. J. Lipid Res. 2010. 51: 564-574.
KW - Polish Collection of Microorganisms
KW - endotoxin
KW - mass spectrometry
KW - palmitoylation
KW - Polish Collection of Microorganisms
KW - endotoxin
KW - mass spectrometry
KW - palmitoylation
UR - https://res.slu.se/id/publ/48606
U2 - 10.1194/jlr.M001362
DO - 10.1194/jlr.M001362
M3 - Journal article
C2 - 19706748
SN - 0022-2275
VL - 51
SP - 564
EP - 574
JO - Journal of Lipid Research
JF - Journal of Lipid Research
IS - 3
ER -