6B Peptides 197
from wine (Moreno-Arribas et al. 1996 1998a,b; Mart ́ınez-Rodr ́ıguez et al. 2002).
Figures 6B.1 and 6B.2 show the chromatograms obtained using this method to sepa-
rate the peptides from the fraction of molecular weight higher (Fig. 6B.1) and lower
(Fig. 6B.2) than 700 Da of one must, one base wine and four sparkling wines (9–12
months of aging) from the Parellada variety.
HPLC has also been used to isolate wine peptides for characterization by other
analytical techniques. Gel filtration chromatography followed by RP-HPLC, using
aμBondasphere C 18 column, was used by Takayanagi and Yokotsuka (1999) to
separate and fractionate several wine peptide fractions. They investigated the amino
acid sequences of the isolated fractionsand also their bioactive capacity using
MMuustst 15m15m
BBaase se winewine 1188 mm
MMuustst
PEPTIDES > 700 Da
15m15m
BBaase se winewine
12m12m12m12m 31m31m31m31m
9m9m9m9m 24m24m24m24m
1188 mm
minminminmin
Absorb
ance
Absorb
ance
(214 (214
nmnm
))
Absorb
ance
Absorb
ance
(214 (214
nmnm
))
Fig. 6B.1HPLC profiles of fraction>700 Da eluted from a Sephadex G-10 column of one must,
one base wine and four sparkling wines of 9, 12, 15 and 18 months of aging with yeast (from
Moreno-Arribas et al. 1996, with permission)