The acclimation of higher plants to different light intensities is associated with a reorganization of the photosynthetic apparatus. These modifications, namely, changes in the amount of peripheral antenna (LHCII) of photosystem (PS) II and changes in PSII/PSI stoichiometry, typically lead to an altered chlorophyll (Chl) a/b ratio. However, our previous studies show that in spruce, this ratio is not affected by changes in growth light intensity. The evolutionary loss of PSII antenna proteins LHCB3 and LHCB6 in the Pinaceae family is another indication that the light acclimation strategy in spruce could be different. Here we show that, unlike Arabidopsis, spruce does not modify its PSII/PSI ratio and PSII antenna size to maximize its photosynthetic performance during light acclimation. Its large PSII antenna consists of many weakly bound LHCIIs, which form effective quenching centers, even at relatively low light. This, together with sensitive photosynthetic control on the level of cytochrome b6f complex (protecting PSI), is the crucial photoprotective mechanism in spruce. High-light acclimation of spruce involves the disruption of PSII macro-organization, reduction of the amount of both PSII and PSI core complexes, synthesis of stress proteins that bind released Chls, and formation of "locked-in" quenching centers from uncoupled LHCIIs. Such response has been previously observed in the evergreen angiosperm Monstera deliciosa exposed to high light. We suggest that, in contrast to annuals, shade-tolerant evergreen land plants have their own strategy to cope with light intensity changes and the hallmark of this strategy is a stable Chl a/b ratio.

• Keywords
• Arabidopsis thaliana, LHCII antenna, Light acclimation, Non-photochemical quenching, Photoprotection, Photosynthetic control, Picea abies, Thylakoid membrane,
• MeSH
• Acclimatization MeSH
• Arabidopsis * metabolism   MeSH
• Chlorophyll A metabolism   MeSH
• Chlorophyll metabolism   MeSH
• Cytochromes b metabolism   MeSH
• Photosystem I Protein Complex metabolism   MeSH
• Photosystem II Protein Complex metabolism   MeSH
• Cytochrome b6f Complex metabolism   MeSH
• Heat-Shock Proteins metabolism   MeSH
• Picea * metabolism   MeSH
• Light MeSH
• Light-Harvesting Protein Complexes metabolism   MeSH
• Publication type
• Journal Article MeSH
• Names of Substances
• Chlorophyll A MeSH
• Chlorophyll MeSH
• Cytochromes b MeSH
• Photosystem I Protein Complex MeSH
• Photosystem II Protein Complex MeSH
• Cytochrome b6f Complex MeSH
• Heat-Shock Proteins MeSH
• Light-Harvesting Protein Complexes MeSH

Photosystem II (PSII) complexes are organized into large supercomplexes with variable amounts of light-harvesting proteins (Lhcb). A typical PSII supercomplex in plants is formed by four trimers of Lhcb proteins (LHCII trimers), which are bound to the PSII core dimer via monomeric antenna proteins. However, the architecture of PSII supercomplexes in Norway spruce[Picea abies (L.) Karst.] is different, most likely due to a lack of two Lhcb proteins, Lhcb6 and Lhcb3. Interestingly, the spruce PSII supercomplex shares similar structural features with its counterpart in the green alga Chlamydomonas reinhardtii [Kouřil et al. (2016) New Phytol. 210, 808-814]. Here we present a single-particle electron microscopy study of isolated PSII supercomplexes from Norway spruce that revealed binding of a variable amount of LHCII trimers to the PSII core dimer at positions that have never been observed in any other plant species so far. The largest spruce PSII supercomplex, which was found to bind eight LHCII trimers, is even larger than the current largest known PSII supercomplex from C. reinhardtii. We have also shown that the spruce PSII supercomplexes can form various types of PSII megacomplexes, which were also identified in intact grana membranes. Some of these large PSII supercomplexes and megacomplexes were identified also in Pinus sylvestris, another representative of the Pinaceae family. The structural variability and complexity of LHCII organization in Pinaceae seems to be related to the absence of Lhcb6 and Lhcb3 in this family, and may be beneficial for the optimization of light-harvesting under varying environmental conditions.

• Keywords
• Picea abies, Pinus sylvestris, clear native polyacrylamide electrophoresis, grana membrane, megacomplex, photosystem II, single-particle electron microscopy, supercomplex,
• MeSH
• Photosystem II Protein Complex chemistry   metabolism   MeSH
• Picea metabolism   MeSH
• Light-Harvesting Protein Complexes chemistry   metabolism   MeSH
• Protein Structure, Tertiary MeSH
• Publication type
• Journal Article MeSH
• Research Support, Non-U.S. Gov't MeSH
• Names of Substances
• Photosystem II Protein Complex MeSH
• Light-Harvesting Protein Complexes MeSH

We explored ability of reflectance vegetation indexes (VIs) related to chlorophyll fluorescence emission (R₆₈₆/R₆₃₀, R₇₄₀/R₈₀₀) and de-epoxidation state of xanthophyll cycle pigments (PRI, calculated as (R₅₃₁- R₅₇₀)/(R₅₃₁-R₅₇₀) to track changes in the CO₂ assimilation rate and Light Use Efficiency (LUE) in montane grassland and Norway spruce forest ecosystems, both at leaf and also canopy level. VIs were measured at two research plots using a ground-based high spatial/spectral resolution imaging spectroscopy technique. No significant relationship between VIs and leaf light-saturated CO₂ assimilation (A(MAX)) was detected in instantaneous measurements of grassland under steady-state irradiance conditions. Once the temporal dimension and daily irradiance variation were included into the experimental setup, statistically significant changes in VIs related to tested physiological parameters were revealed. ΔPRI and Δ(R₆₈₆/R₆₃₀) of grassland plant leaves under dark-to-full sunlight transition in the scale of minutes were significantly related to A(MAX) (R² = 0.51). In the daily course, the variation of VIs measured in one-hour intervals correlated well with the variation of Gross Primary Production (GPP), Net Ecosystem Exchange (NEE), and LUE estimated via the eddy-covariance flux tower. Statistical results were weaker in the case of the grassland ecosystem, with the strongest statistical relation of the index R₆₈₆/R₆₃₀ with NEE and GPP.

• MeSH
• Chlorophyll analysis   MeSH
• Spectrometry, Fluorescence * MeSH
• Photosynthesis physiology   MeSH
• Carbon Cycle physiology   MeSH
• Poaceae physiology   MeSH
• Plant Components, Aerial physiology   MeSH
• Climate MeSH
• Picea physiology   MeSH
• Publication type
• Journal Article MeSH
• Research Support, Non-U.S. Gov't MeSH
• Names of Substances
• Chlorophyll MeSH