We compared the responses of wild type (WT) and three mutants including npq1 (lutein-replete and violaxanthin deepoxidase-deficient), lut2 (lutein-deficient), and lut2-npq1 (double mutant) to high irradiance (HI, 2 000 μmol m-2 s-1) at both low (LT, 5 °C) and room (25 °C) temperature. Xanthophyll-dependent energy dissipation was highest in the WT, followed by the lut2, npq1, and npq1-lut2. At 25 °C the relative stress tolerance expressed by Fv/Fm was consistent with the energy dissipation capacity for the first 2 h of treatment. After 3-4 h, the Fv/Fm levels in lut2 and npq1 converged. Under combined LT and HI the relative tolerance sequence was in contrast to the energy dissipation capacity being WT > npq1> lut2 > lut2-npq1. There were little or no significant change in the contents of xanthophylls and carotenes or the chlorophyll (Chl) a/b ratio in any of the materials. Thus lutein (L) substitution possibly alters the conformation/organisation of L binding proteins to enhance damage susceptibility under HI at LT. The enhanced vulnerability is not compensated for the energy dissipation capacity in the lut2 background at LT. and Chang-Lian Peng, A. M. Gilmore.
We compared photoinhibition sensitivity to high irradiance (HI) in wild-type barley (wt) and both its chlorina f104-nuclear gene mutant, that restricts chlorophyll (Chl) a and Chl b synthesis, and its f2-nuclear gene mutant, that inhibits all Chl b synthesis. Both Fv/Fm and ΦPS2 decreased more significantly in f2 than f104 and wt with duration of HI exposure. Chl degraded more rapidly in the f2 than in either f104 or wt. Most sensitivity to photoinhibition was exhibited for f2, whereas there was little difference in response to HI between the f104 and wt. The highest de-epoxidation (DES) value at every time point of exposure to HI was measured for f2, whereas the wt had the lowest value among the three strains. There were two lifetime components resolved for the conversion of violaxanthin (V) to zeaxanthin plus antheraxanthin (Z + A). The most rapid lifetime was around 6 min and the slower lifetime was >140 min, in both the mutants and wt. However, the wt and f104 both displayed larger amplitudes of both de-epoxidation lifetimes than f2. The difference between the final de-epoxidation state (DES = [Z + A]/[V + A + Z]) in the light compared to the dark expressed as ΔDES for wt, f104, and f2 was 0.630, 0.623, and 0.420, respectively. The slow lifetime component and overall larger ΔDES in the wt and f104 correlated with more photoprotection, as indicated by relatively higher Fv/Fm and ΦPS2, compared to the f2. Hence the photoprotection against photoinhibition has no relationship with the absolute DES value, but there is a strong relationship with de-epoxidation rate and relative extent or ΔDES. and Chang-Lian Peng ... [et al.].