1985
DOI: 10.1016/0308-8146(85)90019-6
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Oxygen involvement in betanine degradation—Measurement of active oxygen species and oxidation reduction potentials

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Cited by 38 publications
(23 citation statements)
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“…467 Moreover, betalains are less susceptible to hydrolytic cleavage (the cleavage of chemical bonds by water addition), see Fig. 472 In 2002, cyclic voltammetry measurements by Butera et al 456 reported for betanin three anodic waves (oxidation) at 0.62, 0.84 and 1.22 V (vs. NHE). 452 In this context, betalains can be an alternative to the less water soluble anthocyanins which under the same pH conditions lose their photochemical properties due to changes of their colours.…”
Section: Betalainsmentioning
confidence: 99%
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“…467 Moreover, betalains are less susceptible to hydrolytic cleavage (the cleavage of chemical bonds by water addition), see Fig. 472 In 2002, cyclic voltammetry measurements by Butera et al 456 reported for betanin three anodic waves (oxidation) at 0.62, 0.84 and 1.22 V (vs. NHE). 452 In this context, betalains can be an alternative to the less water soluble anthocyanins which under the same pH conditions lose their photochemical properties due to changes of their colours.…”
Section: Betalainsmentioning
confidence: 99%
“…Nevertheless, a characterization and clarification of the electron injection mechanism from betalains to TiO 2 , contrary to the case of anthocyanins and chlorophylls, 283,465,466 is missing and the current understanding is mainly correlated to the analysis of the IPCE experiments. 4,172 Since 1985, the redox chemistry of betalains has been investigated, 472 with redox potential values ranging from 0.45 to 0.67 V (vs. NHE). 467 Moreover, betalains are less susceptible to hydrolytic cleavage (the cleavage of chemical bonds by water addition), see Fig.…”
Section: Betalainsmentioning
confidence: 99%
“…, 2004a). Comparing stability of different betacyanins, glycosylated structures are more stable than aglycons, probably because of the higher oxidation–reduction potentials of the former (von Elbe & Attoe, 1985). However, stability does not seem to be enhanced by further glycosylation (Huang & von Elbe, 1986).…”
Section: Factors Affecting Chemical Stability Of Betalainsmentioning
confidence: 99%
“…Comparing the stability of different betacyanin structures, glycosylation was reported to increase the half‐life value of betanidin and isobetanidin by 17 times upon degradation by active oxygen species. This was attributed to the lower oxidation–reduction potential of betanidin as compared to betanin (von Elbe and Attoe 1985). Interestingly, betacyanin stability may not be improved by further glycosylation, since amaranthin (betanidin 5‐ O ‐[2´‐ O ‐(β‐glucuronic acid)]‐β‐glucoside; Figure 1) and betanin were found to exhibit identical stability in the presence of oxygen.…”
Section: Factors Governing Betalain Stabilitymentioning
confidence: 99%
“…Interestingly, oxygen uptake was found to be pH dependent and to increase beyond the pH optimum of betanin (Attoe and von Elbe 1984). Detailed degradation kinetics of betanin as affected by oxygen were established by von Elbe and co‐workers (Attoe and von Elbe 1982, 1984, 1985; von Elbe and Attoe 1985). In addition to oxygen, hydrogen peroxide was also reported to accelerate betanin degradation (Wasserman and others 1984), while betanin stability was shown to be significantly improved in a nitrogen atmosphere (Attoe and von Elbe 1982; von Elbe and Attoe 1985).…”
Section: Factors Governing Betalain Stabilitymentioning
confidence: 99%