The anthocyanins of red onions, Allium cepa L, extraction, characterization, complexation and stabilization.

Using high performance liquid chromatography (HPLC) with a reverse phase column and a photodiode array detector, the chromatographic profiles of the four red onion varieties 'Mambo', 'Red Bone', 'Red Granex' and 'Red Jumbo' were determined. A total of four maj...

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Main Author: Donner, Horst
Language:en_US
Published: 2007
Online Access:http://hdl.handle.net/1993/1129
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spelling ndltd-LACETR-oai-collectionscanada.gc.ca-MWU.1993-11292014-03-29T03:41:20Z The anthocyanins of red onions, Allium cepa L, extraction, characterization, complexation and stabilization. Donner, Horst Using high performance liquid chromatography (HPLC) with a reverse phase column and a photodiode array detector, the chromatographic profiles of the four red onion varieties 'Mambo', 'Red Bone', 'Red Granex' and 'Red Jumbo' were determined. A total of four major and four minor anthocyanins were present in red onions. The anthocyanins and colourless phenolics were identified using a rapid identification procedure based on spectrophotometric, and liquid and gas chromatographic techniques. The major anthocyanins were identified as cyanidin 3-glucoside, cyanidin 3-laminaribioside, cyanidin 3-(6$\sp{\prime\prime}$-malonylglucoside), and cyanidin 3-(6$\sp{\prime\prime}$-malonyllaminaribioside). The four minor anthocyanins were identified as cyanidin 3-(3$\sp{\prime\prime}$-malonylglucoside), peonidin 3-glucoside, pe nidin 3-malonylglucoside and cyanidin 3-dimalonyllaminaribioside. Using the same technique, the colourless phenolic compounds were identified as protocatechuic acid 4-glucoside, quercetin 7,4$\sp\prime$-diglucoside, quercetin 3,4$\sp\prime$-diglucoside, quercetin 3-glucoside, quercetin 4$\sp\prime$-glucoside, and a 5,7-dihydroxy flavanone glucoside or a 5,7-dihydroxy dihydroflavanol glucoside. The copigmentation effect was studied using cyanidin 3-glucoside, cyanidin 3-malonylglucoside, cyanidin 3-malonyllaminaribioside, chlorogenic acid, protocatechuic acid and caffeine in aqueous buffers at pH 3.7, 4.7 and 5.7. It was observed that copigment structure and concentration, and pH have a dramatic influence on the copigmentation phenomenon. Colour stability studies using cyanidin 3-glucoside solutions at pH 3.7, 4.7, and 5.7 without and with added chlorogenic acid, protocatechuic acid and caffeine in the presence and absence of light, demonstrated that intense exposure to fluorescent and incandescent light was detrimental to the photostability of copigmented cyanidin 3-glucoside solutions at any pH. (Abstract shortened by UMI.) 2007-05-15T15:29:46Z 2007-05-15T15:29:46Z 1998-11-01T00:00:00Z http://hdl.handle.net/1993/1129 en_US
collection NDLTD
language en_US
sources NDLTD
description Using high performance liquid chromatography (HPLC) with a reverse phase column and a photodiode array detector, the chromatographic profiles of the four red onion varieties 'Mambo', 'Red Bone', 'Red Granex' and 'Red Jumbo' were determined. A total of four major and four minor anthocyanins were present in red onions. The anthocyanins and colourless phenolics were identified using a rapid identification procedure based on spectrophotometric, and liquid and gas chromatographic techniques. The major anthocyanins were identified as cyanidin 3-glucoside, cyanidin 3-laminaribioside, cyanidin 3-(6$\sp{\prime\prime}$-malonylglucoside), and cyanidin 3-(6$\sp{\prime\prime}$-malonyllaminaribioside). The four minor anthocyanins were identified as cyanidin 3-(3$\sp{\prime\prime}$-malonylglucoside), peonidin 3-glucoside, pe nidin 3-malonylglucoside and cyanidin 3-dimalonyllaminaribioside. Using the same technique, the colourless phenolic compounds were identified as protocatechuic acid 4-glucoside, quercetin 7,4$\sp\prime$-diglucoside, quercetin 3,4$\sp\prime$-diglucoside, quercetin 3-glucoside, quercetin 4$\sp\prime$-glucoside, and a 5,7-dihydroxy flavanone glucoside or a 5,7-dihydroxy dihydroflavanol glucoside. The copigmentation effect was studied using cyanidin 3-glucoside, cyanidin 3-malonylglucoside, cyanidin 3-malonyllaminaribioside, chlorogenic acid, protocatechuic acid and caffeine in aqueous buffers at pH 3.7, 4.7 and 5.7. It was observed that copigment structure and concentration, and pH have a dramatic influence on the copigmentation phenomenon. Colour stability studies using cyanidin 3-glucoside solutions at pH 3.7, 4.7, and 5.7 without and with added chlorogenic acid, protocatechuic acid and caffeine in the presence and absence of light, demonstrated that intense exposure to fluorescent and incandescent light was detrimental to the photostability of copigmented cyanidin 3-glucoside solutions at any pH. (Abstract shortened by UMI.)
author Donner, Horst
spellingShingle Donner, Horst
The anthocyanins of red onions, Allium cepa L, extraction, characterization, complexation and stabilization.
author_facet Donner, Horst
author_sort Donner, Horst
title The anthocyanins of red onions, Allium cepa L, extraction, characterization, complexation and stabilization.
title_short The anthocyanins of red onions, Allium cepa L, extraction, characterization, complexation and stabilization.
title_full The anthocyanins of red onions, Allium cepa L, extraction, characterization, complexation and stabilization.
title_fullStr The anthocyanins of red onions, Allium cepa L, extraction, characterization, complexation and stabilization.
title_full_unstemmed The anthocyanins of red onions, Allium cepa L, extraction, characterization, complexation and stabilization.
title_sort anthocyanins of red onions, allium cepa l, extraction, characterization, complexation and stabilization.
publishDate 2007
url http://hdl.handle.net/1993/1129
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