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Identification of the major drivers of 'phenolic' taste in ... - GWRDC

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AWRI: <strong>Identification</strong> Of The Major Drivers Of ‘Phenolic’ Taste In White W<strong>in</strong>es<br />

keep back pressure under 300 bar and reduce <strong>the</strong> flow rate to 0.13 mL/m<strong>in</strong> dur<strong>in</strong>g <strong>the</strong> high methanol<br />

phase. With two <strong>in</strong> series <strong>the</strong> time taken to elute all peaks has now <strong>in</strong>creased to just over 100 m<strong>in</strong>utes.<br />

To ensure post-run column equilibration was atta<strong>in</strong>ed, a wait time <strong>of</strong> 20 m<strong>in</strong>utes was <strong>in</strong>corporated <strong>in</strong>to<br />

<strong>the</strong> method program, mean<strong>in</strong>g that a complete run lasts 155 m<strong>in</strong>utes (Figure A-1). Us<strong>in</strong>g two columns<br />

<strong>in</strong>creased <strong>the</strong> resolution by a factor <strong>of</strong> two and allowed caffeic acid and one <strong>of</strong> <strong>the</strong> coutaric acid<br />

isomers to be separated. This improvement <strong>in</strong> resolution also allows <strong>the</strong> separation <strong>of</strong> 2-S-glutathionyl<br />

adduct <strong>of</strong> trans-caftaric acid (GRP) from <strong>the</strong> free acid. These are depicted Figure A-2. Unfortunately<br />

<strong>the</strong> resolution between quercet<strong>in</strong>-3-O-glucoside and quercet<strong>in</strong>-3-O-glucuronide is reduced <strong>in</strong> <strong>the</strong> two-<br />

column configuration. Mass spectrometry highlights <strong>the</strong> elution <strong>of</strong> UV-<strong>in</strong>active material elut<strong>in</strong>g 30<br />

m<strong>in</strong>utes after <strong>the</strong> last phenolic peak. This is seen <strong>in</strong> Figure A-3 where <strong>the</strong>re is still a total ion count<br />

(TIC) trace after 110 m<strong>in</strong>utes but no UV absorbance.<br />

106<br />

RS (1x column) RS (2x columns)<br />

trans-caftaric acid + 2-S-glutathionyl trans-caftaric acid (GRP) 1.0 2.3<br />

cis and trans isomers <strong>of</strong> coutaric acid 4.75 8.16<br />

Resolution, RS = (tR1 – tR2) / 0.5(tW1 + tW2) where tR is elution time and tW is tangent basel<strong>in</strong>e width

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