Literature DB >> 15134146

Characterization of epoxy carotenoids by fast atom bombardment collision-induced dissociation MS/MS.

Takashi Maoka1, Yasuhiro Fujiwara, Keiji Hashimoto, Naoshige Akimoto.   

Abstract

The characterization and structure of epoxy carotenoids possessing 5,6-epoxy, 5,8-epoxy and 3,6-epoxy end groups conjugated to the polyene chain were investigated using high-energy fast atom bombardment collision-induced dissociation MS/MS methods. In addition to [M - 80](+*), a characteristic fragment ion of an epoxy carotenoid, product ions resulting from the cleavage of C-C bonds in the polyene chain from the epoxy end group, such as m/z 181 (b ion) and 121 (c ion), were detected. On the other hand, diagnostic ions of m/z 286 (e-H ion) and 312 (f-H ion) were observed, not in the 5,6-epoxy or 5,8-epoxy carotenoid but in the 3,6-epoxy carotenoid. These fragmentation patterns can be used to distinguish 3,6-epoxy carotenoids from 5,6-epoxy or 5,8-epoxy carotenoids. The structure of an epoxy carotenoid, 3,6-epoxy-5,6-dihydro-7',8'-didehydro-beta,beta-carotene-5,3'-diol (8), isolated from oyster, was characterized using FAB CID-MS/MS by comparing fragmentation patterns with those of related known compounds.

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Year:  2004        PMID: 15134146     DOI: 10.1007/s11745-004-1217-3

Source DB:  PubMed          Journal:  Lipids        ISSN: 0024-4201            Impact factor:   1.880


  2 in total

1.  Structures of five new carotenoids from the oyster Crassostrea gigas.

Authors:  T Maoka; K Hashimoto; N Akimoto; Y Fujiwara
Journal:  J Nat Prod       Date:  2001-05       Impact factor: 4.050

2.  Carotenoids of tunicates. III. The structural elucidation of two new marine carotenoids, amarouciaxanthin A and B.

Authors:  T Matsuno; M Ookubo; T Komori
Journal:  J Nat Prod       Date:  1985 Jul-Aug       Impact factor: 4.050

  2 in total

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