Organism name |
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NCBI taxonomy ID |
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Lineage |
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Description |
Land plant: Solanaceae: tomato, same as Lycopersicon esculentum (Primary producer of carotenoids) Japanese
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Carotenoid Profile
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[
Reconstructed carotenoid biosynthesis pathways of the Solanum lycopersicum carotenoids |
Search similar profiled organisms
]
CA00044 Prolycopene
(Ref.123)

CA00060 Phytoene
(Ref.214)

CA00066 (7Z,9Z,9'Z)-Neurosporene
(Ref.296)

CA00071 Lycoxanthin
(Ref.346)

CA00983 (2S,5R,6R)-1,16-didehydro- 2,6-cyclolycopene-5-ol
(Ref.318)

CA00131 Phytofluenol

CA01053 (2S,5S,6R)-1,16-didehydro-2,6-cyclolycopene-5-ol
(Ref.318)

CA01056 (2R,5R,6R)-2,6-cyclolycopene-1,5-diol
(Ref.318)

CA00984 (2S,5S,6R)-2,6-cyclolycopene-1-methoxy-5-ol
(Ref.318)

CA00150 Lycopene 5,6-epoxide

CA00147 ζ-Carotene epoxide
(Ref.346)

CA00151 Phytofluene epoxide
(Ref.346)

CA00148 Phytoene epoxide
(Ref.346)

CA00302 3-Hydroxy-δ-carotene

CA00397 Mutatochrome
(Ref.346)

CA00678 Anhydrolutein I
(Ref.318)

CA00790 Apo-6'-lycopenal

CA00789 Apo-8'-lycopenal

CA01148 Apo-10'-lycopenal
(Ref.694)

CA01219 Apo-12'-lycopenal
(Ref.694)

CA01220 Apo-14'-lycopenal
(Ref.694)

CA01010 Geranylacetone

CA01013 Pseudoionone
(Ref.395)

CA01055 (2S,5S,6R)-plinol
(Ref.318)

CA01011 6-methyl-5-hepten-2-one
(Ref.393)

CA00803 β-Ionone

CA00800 β-Damascenone
(Ref.393)

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References |
Ref.123 : Fantini, Elio; Falcone, Giulia; Frusciante, Sarah; Giliberto, Leonardo; Giuliano, Giovanni, Plant Physiology (2013), 163(2), 986-998., "Dissection of tomato lycopene biosynthesis through virus-induced gene silencing" Ref.214 : Ebenezer, Warren J.; Pattenden, Gerald, Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999) (1993), (16), 1869-73., "cis-Stereoisomers of β-carotene and its congeners in the alga Dunaliella bardawil, and their biogenetic interrelationships" Ref.296 : Tal Isaacson, Itzhak Ohad, Peter Beyer and Joseph Hirschberg, Plant Physiology December 2004 vol. 136 no. 4 4246-4255, doi: http://dx.doi.org/10.1104/pp.104.052092, "Analysis in Vitro of the Enzyme CRTISO Establishes a Poly-cis-Carotenoid Biosynthesis Pathway in Plants" Ref.346 : Avraham Ben-Aziz, George Britton, Trevor W. Goodwin, Phytochemistry, Volume 12, Issue 11, November 1973, Pages 2759-2764, "Carotene epoxides of Lycopersicon esculentum" Ref.318 : Tadashi YOKOTA, Hideo ETOH, Shunji OSHIMA, Kirou HAYAKAWA and Yukio ISHIGURO, Bioscience, Biotechnology, and Biochemistry, Volume 67, Issue 12, 2003, "Oxygenated Lycopene and Dehydrated Lutein in Tomato Puree" Ref.694 : R. E. Kopec et al., J Agric Food Chem. 2010 March 24; 58(6), pp. 3290–3296, "Identification and Quantification of Apo-lycopenals in Fruits, Vegetables, and Human Plasma", doi:10.1021/jf100415z. Ref.395 : Andrew J. Simkin, Steven H. Schwartz, Michele Auldridge, Mark G. Taylor, and Harry J. Klee, The Plant Journal (2004) 40, 882–892, doi: 10.1111/j.1365-313X.2004.02263.x, "The tomato carotenoid cleavage dioxygenase 1 genes contribute to the formation of the flavor volatiles b-ionone, pseudoionone, and geranylacetone" Ref.393 : Jonathan T Vogel, Denise M Tieman, Charles A Sims, Asli Z Odabasi, David G Clark, and Harry J Klee, J Sci Food Agric. 2010 Oct;90(13):2233-40. doi: 10.1002/jsfa.4076., "Carotenoid content impacts flavor acceptability in tomato (Solanum lycopersicum)."
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