Anew structural type for Haemophilus influenzae lipopolysaccharide - Structural analysis of the lipopolysaccharide from nontypeable Haemophilus influenzae strain 486

Citation
M. Mansson et al., Anew structural type for Haemophilus influenzae lipopolysaccharide - Structural analysis of the lipopolysaccharide from nontypeable Haemophilus influenzae strain 486, EUR J BIOCH, 268(7), 2001, pp. 2148-2159
Citations number
49
Categorie Soggetti
Biochemistry & Biophysics
Journal title
EUROPEAN JOURNAL OF BIOCHEMISTRY
ISSN journal
00142956 → ACNP
Volume
268
Issue
7
Year of publication
2001
Pages
2148 - 2159
Database
ISI
SICI code
0014-2956(200104)268:7<2148:ASTFHI>2.0.ZU;2-5
Abstract
Structural elucidation of the sialylated lipopolysaccharide (LPS) of non-ty peable Haemophilus influenzae (NTHi) strain 486 has been achieved by the ap plication of high-field NMR techniques and ESI-MS along with composition an d linkage analyses on O-deacylated LPS and oligosaccharide samples. It was found that the LPS contains the common element of H. influenzae, L-alpha -D -Hepp-(1-->2)][PEtn-->6]-L-alpha -D-Hepp-(1-->3)-[beta -D-Glcp-( 1-->4)]-L- alpha -D-Hepp-(1-->5)- [PPEtn-->4]-alpha -Kdop- (2-->6)-Lipid A, but instea d of glycosyl substitution of the terminal heptose residue (HepIII) at the O2 position observed in other H. influenzae strains, HepIII is chain elonga ted at the O3 position by either lactose or sialyllactose (i.e. alpha -Neu5 Ac(2-->3)-beta -D-Galp-(1-->4)-beta -D-Glcp). The LPS is substituted by an O-acetyl group linked to the O2 position of HepIII and phosphocholine (PCho ) which was located at the O6 position of a terminal alpha -D-Glcp, residue attached to the central heptose, a molecular environment different from wh at has been reported earlier for PCho. In addition, minor substitution by O -linked glycine to the LPS was observed. By investigation of LPS from a lps A mutant of NTHi strain 486, it was demonstrated that the lpsA gene product also is responsible for chain extension from HepIII in this strain. The in volvement of lic1 in expression of PCho was established by investigation of a lic1 mutant of NTHi strain 486.