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IUPAC name ε,ψ-Carotene | |
Systematic IUPAC name (6R)-6--1,5,5-trimethylcyclohex-1-ene | |
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Chemical formula | C40H56 |
Molar mass | 536.873 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references |
δ-Carotene (delta-carotene) or ε,ψ-carotene is a form of carotene with an ε-ring at one end, and the other uncyclized, labelled ψ (psi). It is an intermediate synthesis product in some photosynthetic plants between lycopene and α-carotene (β,ε-carotene) or ε-carotene (ε,ε-carotene). δ-Carotene is fat soluble. Delta-carotene contains an alpha-ionone instead of a beta-ionone ring; this conversion is carried out by the gene Del which shifts the position of the double bond in the ring structure. The formation delta-carotene under the presence of the Del gene is sensitive to high temperatures.
References
- Cunningham FX, Gantt E (February 2001). "One ring or two? Determination of ring number in carotenoids by lycopene epsilon-cyclases". Proceedings of the National Academy of Sciences of the United States of America. 98 (5): 2905–10. doi:10.1073/pnas.051618398. PMC 30238. PMID 11226339.
- Tomes ML (August 1969). "Delta-carotene in the tomato". Genetics. 62 (4): 769–80. doi:10.1093/genetics/62.4.769. PMC 1212314. PMID 17248458.
- Tomes ML (June 1967). "The competitive effect of the Beta- and delta-carotene genes on alpha- or Beta-ionone ring formation in the tomato". Genetics. 56 (2): 227–32. doi:10.1093/genetics/56.2.227. PMC 1211498. PMID 17248383.
Carotenoids | |
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Carotenes (C40) | |
Xanthophylls (C40) | |
Apocarotenoids (C<40) | |
Vitamin A retinoids (C20) | |
Retinoid drugs |
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