Identification of isolutein (lutein epoxide) as cis-antheraxanthin in orange juice

被引:47
作者
Meléndez-Martínez, AJ
Britton, G
Vicario, IM
Heredia, FJ [1 ]
机构
[1] Univ Seville, Lab Food Color & Qual, Dept Nutr & Food Sci, Fac Pharm, E-41012 Seville, Spain
[2] Univ Liverpool, Sch Biol Sci, Liverpool L69 7ZB, Merseyside, England
关键词
antheraxanthin; C-30; carotenoids; isolutein; lutein epoxide; orange juice;
D O I
10.1021/jf051722i
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
The carotenoid profile of orange juice is very complex, a common characteristic for citrus products in general. This fact, along with the inherent acidity of the product, which promotes the isomerization of some carotenoids, makes the correct identification of some of these pigments quite difficult. Thus, one of the carotenoids occurring in orange juice has been traditionally identified as isolutein, a term used to refer to lutein epoxide, although enough evidence to support that identification has not been given. In this study, the carotenoid previously identified as isolutein/lutein epoxide in orange juice has been isolated and identified as a 9 or 9'-cis isomer of antheraxanthin as a result of different tests. To support this identification, a mixture of geometrical isomers of lutein epoxide isolated from petals of dandelions was analyzed under the same conditions used for orange juice carotenoids to check that neither their retention times nor their spectroscopic features matched with those of the orange juice carotenoid now identified as a cis isomer of antheraxanthin.
引用
收藏
页码:9369 / 9373
页数:5
相关论文
共 41 条
[1]  
[Anonymous], 1999, ARCH LATINOAM NUTR
[2]  
[Anonymous], THESIS U SEVILLA
[3]  
[Anonymous], CLOROFILAS CAROTENOI
[4]   Xanthophyll epoxides, unlike β-carotene monoepoxides, are not detectibly absorbed by humans [J].
Barua, AB ;
Olson, JA .
JOURNAL OF NUTRITION, 2001, 131 (12) :3212-3215
[5]   Improved normal-phase and reversed-phase gradient high-performance liquid chromatography procedures for the analysis of retinoids and carotenoids in human serum, plant and animal tissues [J].
Barua, AB .
JOURNAL OF CHROMATOGRAPHY A, 2001, 936 (1-2) :71-82
[6]   Chromatographic performance on a C30-bonded stationary phase of monohydroxycarotenoids with variable chain length or degree of desaturation and of lycopene isomers synthesized by various carotene desaturases [J].
Breitenbach, J ;
Braun, G ;
Steiger, S ;
Sandmann, G .
JOURNAL OF CHROMATOGRAPHY A, 2001, 936 (1-2) :59-69
[7]  
Britton G., 1995, Carotenoids, Volume 1A: Isolation and Analysis, V1A
[8]  
Britton G., 1993, CAROTENOIDS PHOTOSYN, P409
[9]  
Britton G, 1991, METHODS PLANT BIOCH, P473
[10]  
Britton G, 1995, CAROTENOIDS A, P201