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. 2018 May 3;69(11):2823–2835. doi: 10.1093/jxb/ery170

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© The Author(s) 2018. Published by Oxford University Press on behalf of the Society for Experimental Biology.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

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Fig. 4. — The pigment composition of the vtc2-1 and vtc2-4 leaves compared with the wild type (WT). Plants were grown under low light (LL; 250 μmol m^-2 s^-1) conditions for 5 weeks and then either for a further 7 d under LL conditions or after transfer to high light (HL; 1600 μmol m^–2 s^–1) growth conditions for 7 d. Leaves were harvested from plants grown only under LL, after 7 d growth under HL, and after ‘recovery’ (2 d after return to the LL growth environment after 7 d under HL). De-epoxidation state (DEPs)=(Z+0.5A)/(V+A+Z); XC: xanthophyll pool (Z+A+V)/(Z+A+V+N+L+β-car) where Z, zeaxanthin; V, violaxanthin; A, antheraxanthin; N, neoxanthin; L, lutein; β-car, β-carotene. Data are presented as means ± SEM from five replicates. * indicates significantly different results during each experimental time point according to ANOVA, P<0.05.