ABSTRACT
The distribution of sugars is crucial for plant energy, signaling, and defense mechanisms. Sugar Transport Proteins (STPs) are Sugar Porters that enable the proton-driven cellular uptake of glucose. A few STPs also import fructose, but what determine this shift in specificity between chemically highly similar compounds remain unknown. In this study, we present the structure of Arabidopsis thaliana STP6 in an inward occluded conformational state with glucose bound and demonstrate its role as both a glucose and fructose transporter. We perform a comparative analysis of STP6 with the glucose-selective STP10 using in-vivo and in-vitro systems, demonstrating how different experimental setups strongly influence kinetic transport properties. Finally, we show that the position of a single methyl group in the binding site is sufficient to shuffle glucose and fructose specificity, providing detailed insights into the fine-tuned dynamics of affinity-induced specificity for sugar uptake. Altogether these findings enhance our understanding of sugar trafficking by Sugar Transport Proteins and lay the groundwork for the future advancements need to support plant engineering and enhance resistance towards pathogens.
Competing Interest Statement
The authors have declared no competing interest.
Footnotes
Fixed typos and rearranged a number of figures for clarity.
