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Ascorbic Acid
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Supercritical Fluid Chromatography
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Supercritical fluid chromatography as a method of analysis for the determination of 4-hydroxybenzylglucosinolate degradation products
Supercritical fluid chromatography as a method of analysis for the determination of 4-hydroxybenzylglucosinolate degradation products,10.1016/S0165-02
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Supercritical fluid chromatography as a method of analysis for the determination of 4-hydroxybenzylglucosinolate degradation products
(
Citations: 15
)
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Steen Buskov
,
Jørgen Hasselstrøm
,
Carl Erik Olsen
,
Hilmer Sørensen
,
Jens Christian Sørensen
,
Susanne Sørensen
In the present study analytical and preparative
supercritical fluid chromatography
(SFC) were used for investigation of myrosinase catalysed degradation of 4-hydroxybenzylglucosinolate (sinalbin). Sinalbin occurs as a major glucosinolate in seeds of Sinapis alba L., in various mustards and other food products. The degradation products were identified and quantified by analysis based on a developed SFC method using a bare
silica
column. Determinations comprised transformation products of sinalbin, produced both during degradation of isolated sinalbin, and during autolysis of meal from S. alba seeds. The conditions in the developed SFC method were used as basis for the preparative SFC procedure applied for isolation of the components prior to their identification by
nuclear magnetic resonance
(NMR) spectroscopy. Myrosinase catalysed sinalbin hydrolysis resulted in the reactive 4-hydroxybenzyl isothiocyanate as an initial product at pH values from 3.5 to 7.5 whereas 4-hydroxybenzyl cyanide was one of the major products at low pH values. 4-Hydroxybenzyl isothiocyanate was found to disappear from the aqueous reaction mixtures in a few hours, as it reacted easily with available nucleophilic reagents. 4-Hydroxybenzyl alcohol was found as the product from reaction with water, and with ascorbic acid, 4-hydroxybenzylascorbigen was produced.
Journal:
Journal of Biochemical and Biophysical Methods - J BIOCHEM BIOPHYS METH
, vol. 43, no. 1, pp. 157-174, 2000
DOI:
10.1016/S0165-022X(00)00081-6
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Citation Context
(3)
...In accordance, HBC has indeed been detected as a sinalbin hydrolysis product (
Buskov et al. 2000
)...
Caroline Müller
,
et al.
Lack of sequestration of host plant glucosinolates in Pieris rapae an...
...Conversely, in the human diet, they can also have positive physiological effects (Bjergegaard et al., 1994,
Buskov et al., 2000a,
b, and refs...
J. Hill
,
et al.
Inheritance of progoitrin and total aliphatic glucosinolates in oilsee...
...The released aglucones form a variety of biologically active products with structures defined by the type of glucosinolate and the reaction conditions (Bjergegaard et al., 1994;
Buskov et al., 2000a;
Buskov et al., 2000b; Buskov et al., 2000c; Palmieri et al., 1998)...
...Determining the type of glucosinolates present in a certain species might be the first step for the assessment of its biofumigation potential, since transformation products resulting from glucosinolate hydrolysis have different toxicities due to their variation in structural types, physical and chemical properties (Bjergegaard et al., 1994;
Buskov et al., 2000a;
Buskov et al., 2000b; Buskov et al., 2000c; Palmieri et al., 1998)...
Natalia Bellostas
,
et al.
Qualitative and quantitative evaluation of glucosinolates in crucifero...
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