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Review
. 2020 Jan;74(1):1-16.
doi: 10.1007/s11418-019-01364-x. Epub 2019 Oct 1.

Carotenoids as natural functional pigments

Affiliations
Review

Carotenoids as natural functional pigments

Takashi Maoka. J Nat Med. 2020 Jan.

Abstract

Carotenoids are tetraterpene pigments that are distributed in photosynthetic bacteria, some species of archaea and fungi, algae, plants, and animals. About 850 naturally occurring carotenoids had been reported up until 2018. Photosynthetic bacteria, fungi, algae, and plants can synthesize carotenoids de novo. Carotenoids are essential pigments in photosynthetic organs along with chlorophylls. Carotenoids also act as photo-protectors, antioxidants, color attractants, and precursors of plant hormones in non-photosynthetic organs of plants. Animals cannot synthesize carotenoids de novo, and so those found in animals are either directly accumulated from food or partly modified through metabolic reactions. So, animal carotenoids show structural diversity. Carotenoids in animals play important roles such precursors of vitamin A, photo-protectors, antioxidants, enhancers of immunity, and contributors to reproduction. In the present review, I describe the structural diversity, function, biosyntheses, and metabolism of natural carotenoids.

Keywords: Biosyntheses; Carotenoids; Function; Metabolism; Natural pigments.

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Conflict of interest statement

No conflict of interests for the author.

Figures

Fig. 1
Fig. 1
a Basic structures of carotenoids and end groups. b Structures of typical carotenes and xanthophylls
Fig. 2
Fig. 2
a Carotenoid biosynthetic pathways (formation of phytoene). b Desaturation of polyene chain and cyclization of end groups
Fig. 3
Fig. 3
Xanthophyll cycles
Fig. 4
Fig. 4
a Formation of tobiraxanthin and b formation of pittosporumxanthins in the seeds of Pittosporum tobira
Fig. 5
Fig. 5
a Metabolic pathways of fucoxanthin in bivalves and tunicates. b Metabolic conversion mechanisms of end groups of fucoxanthin in bivalves and tunicates
Fig. 6
Fig. 6
Metabolic pathways of peridinin in bivalves and tunicates
Fig. 7
Fig. 7
Oxidative metabolism of β-carotene in crustaceans
Fig. 8
Fig. 8
Metabolic conversion of zeaxanthin to (3S,3′S)-astaxanthin in Cyprinidae fish
Fig. 9
Fig. 9
Reductive metabolic pathway of astaxanthin in marine fish
Fig. 10
Fig. 10
Food chain and metabolism of carotenoids in sea angel
Fig. 11
Fig. 11
Novel carotenoid pyropheophorbide A ester from abalone
Fig. 12
Fig. 12
Carotenoid biosynthetic pathways by horizontal transfer genes from fungi and symbiotic bacteria in aphid and whitefly
Fig. 13
Fig. 13
Oxidation pathway of xanthophylls with 3-hydroxy-β-end in mammals
Fig. 14
Fig. 14
Auto oxidation products of astaxanthin and reaction products of astaxanthin with peroxynitrite
Fig. 15
Fig. 15
Reaction products of ataxanthin with hydroxy radicals, superoxide anion radicals, and singlet oxygen

References

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