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. 2004 Dec;136(4):4246–4255. doi: 10.1104/pp.104.052092

Table I.

Absorption spectra of carotenoids in the HPLC analysis

Peak No. in Chromatogram in Figure 3 Carotenoid λ max nma % III/IIab
1a trans-Lycopene 449, 474, 503 63
1b Di-cis-lycopene 450, 474 0
2 Prolycopene 440 0
3a Neurosporene isomer 1 419, 440, 470 83
3b Neurosporene isomer 2 417, 440, 469 56
3c 7,9,9′-cis-Neurosporene 411, 435, 463 0
4a 9,15,9′-cis-ζ-Carotene (297), 380, 401, 425 76
4b 9,9′-cis-ζ-Carotene 380, 401, 425 95
5a β-Carotene isomer 1 455, 484 13
5b β-Carotene isomer 2 450, 476 0
6 Phytofluene 331, 350, 367 62
7 Phytoene 288 0
Standard trans-Lycopene 449, 474, 503 62
Standard trans-Neurosporene 420, 445, 474 90
Standard trans-ζ-Carotene 380, 401, 425 95
Standard trans-β-Carotene 430, 455, 484 21
a

Absorbance spectra as detected in the HPLC running solvent: a gradient of acetonitrile:water (9:1) and ethylacetate (HPLC system 2).

b

% III/II, Fine structure of the absorption spectra expressed as the relative heights of the longest wavelength peak (III) to the middle peak (II). Zero means lack of peak III.