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Lipopolysaccharide


DATA No : CLS1411 INFORMANT : Yoshio Kumazawa

NAME : 2'N-3''(undecanoyloxy)tridecanoyl, 3'-O-3''(undecanoyloxy)tridodecanoyl b-(1a_right6) D-glucosaminyl 2N-3''hydroxytridecanoyl, 3-O-3''hydroxytridecanoyl D-glucosamine 1-phosphate, 4'-4''-amino-4-deoxyarabinose-phosphate

COMMON NAME:
SYMBOL:
FORMULA: C97H181O28N3P2 MOL.WT (average) : 1899.426


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BIOLOGICAL ACTIVITY
Susceptibility of P. cerevisiiphilus
[Table 0037]
PHYSICAL AND CHEMICAL PROPERTIES
MELTING POINT:

BOILING POINT:

REFRACTIVE INDEX:

OPTICAL ROTATION:

DENSITY:

SOLUBILITY:
SPECTRAL DATA
UV SPECTRA:

IR SPECTRA:

NMR SPECTRA:31P-NMR spectra of de-O-acylated lipopolysaccharide
[Spectrum 0037]

MASS SPECTRA:Positive ion LD-MS of free dephosphorylated lipid A
[Spectrum 0038]
Assignment of peaks in the LD mass spectra of free dephosphorylated lipid A
[Table 0036]
Interpretation of the fragmentation pattern of free dephosphorylated lipid A
[Spectrum 0039]

OTHER SPECTRA:
CHROMATOGRAM DATA

SOURCE
Pectinatus cerevisiiphilus and Pectinatus frisingensis(Ref. 1411)
CHEMICAL SYNTHESIS

METABOLISM

GENETIC INFORMATION

NOTE
Partial chemical composition of P. cerevisiiphilus lipopolysaccharide and subsequent degradation products
[Table 0035]
REFERENCES
[1411]
AUTHOR:Helander I M., Kilpelainen I, Vaara M, Moran AP, Lindner B, Seydel U
TITLE:Chemical structure of the lipid A of lipopolysaccharide of the genus Pectinatus. PubMed ID:8076652
JOURNAL: Eur J Biochem
VOL:224 PAGE : 63 -70 (1994)
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Last updated June 19, 2007. Copyright © 1989-2007 Japanese Conference on the Biochemistry of Lipids (JCBL). All rights reserved.