Two novel glycolipids, docosanyl 3-O-methyl-alpha -rhamnopyranoside and doc
osanyl 3-O-methylxylopyranoside, were identified as the most abundant GC-am
enable components of extracts of sediments of Ace Lake, an Antarctic meromi
ctic lake. Docosanyl 3-O-methyl-alpha -rhamnopyranoside was identified by i
solation and high-field two-dimensional NMR techniques. Docosanyl 3-O-methy
lxylopyranoside was tentatively identified by characterisation of its sugar
moiety by methanolysis and demethylation. Both glycolipids also have a min
or homologue, containing a C-24 instead of a C-22 n-alkyl chain. Stable car
bon isotope measurements indicate that the sugar moieties of these glycolip
ids are ca. 8-9 parts per thousand enriched relative to the alkyl chains. C
oncentrations increased markedly with depth reaching 2 mg/g sediment at 25
cm depth. Structurally related glycolipids occur in specialised cells of ni
trogen-fixing cyanobacteria, so a cyanobacterial origin is suggested for th
ese sedimentary glycolipids. (C) 2001 Elsevier Science Ltd. All rights rese
rved.