The distribution of the photosynthetic pigments of the chlorophyll-binding proteins or photosystem-II membranes, isolated from dark-adapted maize leaves was determined. Most (80%) of a xanthophyll, violaxanthin, was found in the three minor chlorophyll-ulb proteins CP24, CP26 and CP29 whose function is unknown. Violaxanthin is the precursor of zeaxanthin, which is involved in dissipating excess excitation energy into heat [Demmig-Adams, B. (1991) . We propose that a role for the minor photosystem-II chlorophyll-ulb proteins is the regulation of energy transfer to the reaction centre. It was also confirmed that the photosystem I1 reaction centre (Dl-D2-~ytochrome b5.59) contains pcarotene as the only carotenoid. However, the two other chlorophyll-a-binding proteins of photosystem 11, CP47 and CP43, bind not only p-carotene, but also the xanthophyll lutein, previously thought to be restricted to chlorophyll-ulb proteins.In green plants, light harvesting and photosynthetic electron transport occur in the thylakoids, which are the predominant membranes in plant leaf cells representing up to 80% of the total membrane [l] in a mesophyll cell. Thylakoids are organized into two major functional regions : the appressed or grana membranes and the non-appressed or stroma membranes, which contain different electron-transport components and pigment-binding complexes participating in the photosynthetic process.In both membrane domains, the photosynthetic pigments have four functions : light harvesting, energy transfer, energy dissipation and charge separation [2-41. Charge separation is restricted to the primary chromophore chlorophyll a, while photoprotection through energy dissipation is a carotenoid function, owing to the low energy levels of their triplet states with respect to those of chlorophyll. The role of the pigments in each of the functions listed above depends on the different features of their molecular structures. For example, energy transfer from carotenoids to chlorophylls occurs through singlet-singlet excitation-energy transfer while triplet-triplet interactions are involved in photoprotection. The characteristics of the energetic transitions involved are determined by the covalent molecular structure of the pigments and by their interactions with the polypeptides to which they are bound. The latter can be regarded as a fine tuning process to modify their function. The properties of the photosynthetic pigments in vivo are different from those in solution, the absorbance Abbreviations. PSII core, chlorophyll a complex containing D1, D2, cytochrome b559, CP43, CP47 ; Cab, chlorophyll-u/b proteins; CP, chlorophyll-protein complex; PSII, photosystem I1 ; LHCII, the major light-harvesting complex of PSII; 0. E. E., oxygen evolving enhancer.ste 75, 1-35121 Padova, Italy maxima being red-shifted up to about 30 nm, probably due to the influence of charged residues in the polypeptide(s) [5]; however, shifts due to a transmembrane electric field caused by a pH gradient have also been reported, accounting for a poss...