STUDIES ON THE AROMA FORMATION MECHANISM OF OOLONG TEA .3. TRANS-LINALOOL AND CIS-LINALOOL 3,6-OXIDE 6-O-BETA-D-XYLOPYRANOSYL-BETA-D-GLUCOPYRANOSIDES ISOLATED AS AROMA PRECURSORS FROM LEAVES FOR OOLONG TEA
Jh. Moon et al., STUDIES ON THE AROMA FORMATION MECHANISM OF OOLONG TEA .3. TRANS-LINALOOL AND CIS-LINALOOL 3,6-OXIDE 6-O-BETA-D-XYLOPYRANOSYL-BETA-D-GLUCOPYRANOSIDES ISOLATED AS AROMA PRECURSORS FROM LEAVES FOR OOLONG TEA, Bioscience, biotechnology, and biochemistry, 58(9), 1994, pp. 1742-1744
New glycosidic aroma precursors (1 and 2) of the main volatile constit
uents, trans- and cis-linalool 3,6-oxides (linalool oxides I and II),
were isolated from oolong tea leaves (Camellia sinensis var. sinensis
cv. Maoxie). The isolation was guided by an enzymatic hydrolysis with
acetone powder prepared from fresh tea leaves (cv. Yabukita) followed
by GC or GC-MS analyses. Chromatographic purification of hot water ext
racts of the tea leaves on active charcoal, Amberlite XAD-2, and Sepha
dex LH-20 columns as well as HPLC gave two new glycosides, trans- and
cis-linalool 3,6-oxide 6-O-beta-D-xylopyranosyl-beta-D-glucopyranoside
s (1 and 2).