| Abstract
| - A total of 570 lyophilised Brassica root and shoot tissue samples were hydrolyzed, and the liberatedisothiocyanates (ITCs) were analyzed by gas chromatography−flame photometric detection (GC−FPD). Glucosinolates (GSLs) were extracted from samples of the same tissues and analyzed by high-performance liquid chromatography (HPLC). The concentrations of six GSLs/ITCs (2-propenyl,3-butyl, 4-pentenyl, benzyl, 4-methylthiobutyl, and 2-phenylethyl) as determined by the twotechniques were compared. In 79% of the samples, the concentration of GSLs in the tissues wasgreater than that of the ITCs released on hydrolysis. Several possible reasons for the difference areproposed, including the effect of tissue storage time, hydrolysis of GSLs may be less efficient thanthe GSL extraction procedure, or some of the ITCs formed reacted with plant proteins and aminoacids in the sample and were therefore not detected in the extract. GSL concentration in planttissues is used to estimate the biofumigation potential of the plant tissue, whereas the actualbiofumigation effect is thought to be due to the ITCs formed by hydrolysis of the plant-based GSLs.The variation between ITC and GSL values therefore has implications for the assessment of thebiofumigation potential of the plant tissue. Keywords: Isothiocyanates; glucosinolates; hydrolysis; biofumigation; brassicas; GC; HPLC
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