To investigate vanillin glucoside accumulation in Vanilla planifolia, pod samples at various developmental stages after pollination were sectioned and analyzed using analytical chemistry techniques. This approach enabled us to track the vanillin glucoside accumulation over time and select optimal time points for gene expression analysis through transcriptomics. As a result, we identified a list of co-expressed genes that follow the same accumulation pattern as vanillin glucoside, increasing in concentration in the inner pod tissue over time but absent in leaf tissue.
For Sorghum bicolor, we developed a method to isolate and separate different cell types from seedling leaves. Cell isolation techniques were combined with flow cytometry, using size and chlorophyll autofluorescence as a sorting parameter to distinguish between epidermal and mesophyll cells. This approach successfully yielded two distinct cell populations for further chemical and proteomic analysis. Our findings confirmed that dhurrin is predominantly stored in epidermal cells, but the proteins involved in its metabolism did not exhibit a clear distribution pattern, suggesting the involvement of alternative transport mechanisms. Additionally, we optimized cell isolation protocols to enable transient transformation with fluorescently tagged dhurrin-related proteins, allowing us to determine their subcellular localization through microscopy.