Screening crucifer seeds as sources of specific intact glucosinolates using ion-pair high-performance liquid chromatography negative ion electrospray mass spectrometry

被引:166
作者
Bennett, RN [1 ]
Mellon, FA [1 ]
Kroon, PA [1 ]
机构
[1] Inst Food Res, Norwich NR4 7UA, Norfolk, England
关键词
glucosinolates; seeds; standards; functional foods; LC-MS;
D O I
10.1021/jf030530p
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Seeds, of either commercial crucifer crops or some wild and weed relatives, were screened for intact glucosinolates using a previously developed ion-pair LC-MS method. This method, in contrast to GC-MS techniques, ensures the accurate measurement of all classes of glucosinolates. Many crucifer seeds contained very high concentrations of glucosinolates with low concentrations of additional pigments and secondary metabolites. The other common seed metabolites were cinnamoylcholine esters, for example, sinapine. Glucosinolates derived from homologues of L-methionine were characteristic of Brassica and related crucifer species. In addition, significant concentrations of 4-hydroxy-3-indolylmethyl-glucosinolate were found in the majority of Brassica species. Wild and weed species often had relatively simple glucosinolate profiles: either a single glucosinolate or a predominant glucosinolate together with trace amounts of others. Species identified with seed glucosinolate profiles suitable for purification included various Alyssum, Erysimum, and Iberis species for 3-methythiopropyl-glucosinolate and 3-methylsulfinylpropyl-glucosinolate and various Alyssum, Erysimum, and Lepidium species with very high concentrations of C4-C6 aliphatic glucosinolates. Seeds of Arabis, Barbarea, Lepidium, Moringa, and Sinapis species were good sources of aromatic glucosinolates, and Azima tetracantha was a good source for N-methoxy-3-indolylmethyl-glucosinolate. MS data are reported for all of the intact glucosinolates detected from the screening process.
引用
收藏
页码:428 / 438
页数:11
相关论文
共 52 条
[1]  
AGEBIRK N, 1998, J AGR FOOD CHEM, V46, P1563
[2]   Sulforaphane and its glutathione conjugate but not sulforaphane nitrile induce UDP-glucuronosyl transferase (UGT1A1) and glutathione transferase (GSTA1) in cultured cells [J].
Basten, GP ;
Bao, YP ;
Williamson, G .
CARCINOGENESIS, 2002, 23 (08) :1399-1404
[3]   Biosynthesis of benzylglucosinolate, cyanogenic glucosides and phenylpropanoids in Carica papaya [J].
Bennett, RN ;
Kiddle, G ;
Wallsgrove, RM .
PHYTOCHEMISTRY, 1997, 45 (01) :59-66
[4]   Profiling glucosinolates and phenolics in vegetative and reproductive tissues of the multi-purpose trees Moringa oleifera L. (horseradish tree) and Moringa stenopetala L. [J].
Bennett, RN ;
Mellon, FA ;
Foidl, N ;
Pratt, JH ;
Dupont, MS ;
Perkins, L ;
Kroon, PA .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2003, 51 (12) :3546-3553
[5]   Identification of the major glucosinolate (4-mercaptobutyl glucosinolate) in leaves of Eruca sativa L. (salad rocket) [J].
Bennett, RN ;
Mellon, FA ;
Botting, NP ;
Eagles, J ;
Rosa, EAS ;
Williamson, G .
PHYTOCHEMISTRY, 2002, 61 (01) :25-30
[6]   Micellar electrokinetic capillary chromatography of thiocarbamoyl derivatives produced in reactions between isothiocyanates and amino acids [J].
Bjergegaard, C ;
Moller, P ;
Sorensen, H ;
Sorensen, JC ;
Sorensen, S .
JOURNAL OF CHROMATOGRAPHY A, 1999, 836 (01) :115-127
[7]  
Bones AM, 1996, PHYSIOL PLANTARUM, V97, P194, DOI 10.1111/j.1399-3054.1996.tb00497.x
[8]   Effects of benzyl isothiocyanate and 2-phenethyl isothiocyanate on benzo[a]pyrene and 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone metabolism in F-344 rats [J].
Boysen, G ;
Kenney, PMJ ;
Upadhyaya, P ;
Wang, MY ;
Hecht, SS .
CARCINOGENESIS, 2003, 24 (03) :517-525
[9]  
Bushkov S., 2000, J AGR FOOD CHEM, V48, P2693
[10]   In vitro and in vivo inhibition of human flavin-containing monooxygenase form 3 (FMO3) in the presence of dietary indoles [J].
Cashman, JR ;
Xiong, Y ;
Lin, J ;
Verhagen, H ;
van Poppel, G ;
van Bladeren, PJ ;
Larsen-Su, S ;
Williams, DE .
BIOCHEMICAL PHARMACOLOGY, 1999, 58 (06) :1047-1055