The authors introduce the ENABLE(R) Gene Editing in planta toolkit, a streamlined two‑step cloning system for creating CRISPR/Cas9 knockout vectors suitable for transient or stable transformation. Validation was performed in Oryza sativa protoplasts and Arabidopsis thaliana plants, and the toolkit includes low‑cost protocols aimed at facilitating adoption in the Global South.

The study examined how tricarboxylic acid (TCA) cycle metabolites influence drought tolerance in grapevine and Arabidopsis, finding that malate uniquely triggers stomatal closure via elevations in cytosolic Ca2+ and activation of the SLAC1 anion channel. G-proteins were shown to be essential for malate‑mediated signaling, linking metabolic changes to drought response through a second‑messenger cascade.