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van den Berg, T. E.

Publications and source records attributed to van den Berg, T. E..

2 recordsLinked to original sources

Viewing stomata in action: Autonomous in planta imaging of individual stomatal movement links morphology and kinetics

Stomata regulate plant gas exchange under changing environments, but observations of the dynamics of single stomata in planta are sparse. We developed a compact microscope system that can measure the kinetics of tens of stomata in planta simultaneously, with sub-minute time resolution. Dark field imaging with green light was used to create 3D stacks from which 2D surface projection were constructed to resolve stomatal apertures within the field of view. Stomatal dynamics of Chrysanthemum morifolium (Chrysanthemum) and Zea Mays (Maize) under dynamically changing light intensity were categorized, and a kinetic model was fitted to the data for quantitative comparison. In addition, we also resolved dynamics of the surface position of the leaf, related to dynamics of leaf thickness or bending. Maize stomata oscillated frequently between open and closed states under constant growth light and these oscillating stomata responded faster to changes in light than non-oscillating stomata at the same aperture. The slow closure of Chrysanthemum stomata reduced water use efficiency (WUE). Over 50% showed delayed or partial closure, leading to unnecessarily large apertures after reduced light. Stomata with larger apertures had more lag and similar closure speeds compared to those with smaller apertures and lag, further reducing WUE. In contrast, maize stomata with larger apertures closed faster, with no lag. In conclusion, our new system enables fine mapping of the heterogeneity of movement in neighboring stomata, providing new insights on the relations between stomatal dimensions, relative position and aperture changes under fluctuating light intensity.

plant biology↗

The Loroxanthin cycle: A new type of xanthophyll cycle in green algae (Chlorophyta)

Xanthophyll cycles have proven to be major contributors to photoacclimation for many organisms. This work describes a light-driven xanthophyll cycle operating in the chlorophyte Chlamydomonas reinhardtii and involving the xanthophylls Lutein (L) and Loroxanthin (Lo). Pigments were quantified during a switch from high to low light and at different time points from cells grown in Day/night cycle. Trimeric LHCII was purified from cells acclimated to high or low light and their pigment content and spectroscopic properties were characterized. The Lo/(L+Lo) ratio in the cells varies by a factor of 10 between cells grown in low or high light leading to a change in the Lo/(L+Lo) ratio in trimeric LHCII from 0.5 in low light to 0.07 in high light. Trimeric LhcbMs binding Loroxanthin have 5{+/-}1% higher excitation energy transfer from carotenoid to Chlorophyll as well as higher thermo- and photostability than trimeric LhcbMs that only bind Lutein. The Loroxanthin cycle operates on long time scales (hours to days) and likely evolved as a shade adaptation. It has many similarities with the Lutein-epoxide - Lutein cycle of plants.

plant biology↗