Abstract
The identification of novel herbicides is of crucial importance to modern agriculture. We developed an efficient in vivo assay based on oxygen evolution measurements using suspensions of chlorenchyma cells isolated from the single-cell C4 plant Bienertia sinuspersici to identify and characterize inhibitors of C4 photosynthesis. This novel approach fills the gap between conventional in vitro assays for inhibitors targeting C4 key enzymes and in vivo experiments on whole plants. The assay addresses inhibition of the target enzymes in a plant context thereby taking care of any reduced target inhibition due to metabolization or inadequate uptake of small molecule inhibitors across plant cell walls and membranes. Known small molecule inhibitors targeting C4 photosynthesis were used to validate the approach. To this end, we tested pyruvate phosphate dikinase inhibitor bisindolylmaleimide IV and phosphoenolpyruvate carboxylase inhibitor okanin. Both inhibitors show inhibition of plant photosynthesis at half-maximal inhibitory concentrations in the sub-mM range and confirm their potential to act as a new class of C4 selective inhibitors.
Highlights
A number of different types of photosynthesis — C3, C4, and crassulacean acid metabolism (CAM) — are known for terrestrial plants
The photosynthetic activity of B. sinuspersici chlorenchyma cell suspensions was determined by a Clark type oxygen electrode as described above
The yields of typical preparations were in the range of 1,000 to 7,200 intact cells per leaf judged by trypan blue staining
Summary
A number of different types of photosynthesis — C3, C4, and crassulacean acid metabolism (CAM) — are known for terrestrial plants. CAM and C4 plants adapted to hot and dry climate by establishing CO2 concentrating mechanisms that circumvent the oxygenase reactivity of ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBisCO) which is the key enzyme of photosynthetic carbon fixation within the Calvin-Benson-Bassham (CBB) cycle. In C4 plants, this CO2 concentrating mechanism is implemented by a spatial separation of CO2 uptake from the CBB cycle. This separation is established across two cell types: bundle sheath (BS) cells which are surrounded by a layer of leaf mesophyll (LM) cells forming the so-called Kranz anatomy. Primary CO2 fixation takes place in the LM cells, where atmospheric CO2 is fixed after conversion to HCO3− by phosphoenolpyruvate carboxylase (PEPC) yielding the four-carbon organic acid
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