Steryl esters make up a major portion of the total lipids in aspen wood, an
d contribute significantly to pitch deposit problems during pulping. Fungal
treatment of aspen is an attractive method for removing these compounds be
cause it is inexpensive and environmentally acceptable; however, the mechan
ism of steryl ester removal remains unclear. Identification of the steryl e
sters will lead to a better understanding of how they are removed by fungi.
The steryl ester fraction from aspen wood was obtained by acetone extracti
on then further purified by silica gel column chromatography and argentatio
n-silica gel column chromatography. This led to the isolation of three majo
r fractions: fraction I, fraction II, and fraction III. The major steryl es
ters of fractions I and ii were identified by gas chromatography, gas chrom
atography-mass spectroscopy, and proton nuclear magnetic resonance analysis
of the intact fraction as well as sterol and fatty acid moieties obtained
after base hydrolysis. Identification of the steryl esters was carried out
by mass spectra comparisons with steryl ester standards synthesized in the
laboratory and comparison with mass spectra libraries (Wiley and NIST) by m
ass fragmentography. Fraction I contained primarily the palmitate, stearate
, and eicosanoate esters of alpha- and beta-amyrin. Fraction II consisted m
ainly of the palmitate, stearate, and eicosanoate esters of tirucalla-7,24-
dien-3 beta-ol and lupeol.