Identification of interacting proteins of Arabidopsis cyclophilin38 (AtCYP38) via multiple screening approaches reveals its possible broad functions in chloroplasts.
This article investigates physiological roles of AtCYP38 and analyses the ultrastructure of chloroplasts from cyp38-2 plants. Transmission electron microscopy followed by quantitative micrography revealed modifications in thylakoid stacking. The depletion of AtCYP38 influences PSII performance which leads to stunted phenotype of cyp38-2 plants.
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