Carbohydrate uptake from xylem vessels and its distribution among stem tissues and buds in walnut (Juglans regia L.).

Bud break pattern is a key determinant of tree architecture. The mechanisms leading to the precedence of certain buds over the others are not yet fully explained, but the availability of soluble sugars may play a significant role, especially those in the xylem sap at the onset of the growing period. Here, we measured carbon availability in the different tissues (bud, xylem and bark). To assess the capacity of buds to use the xylem sap carbohydrates, the fluxes between xylem vessels and parenchyma cells, bark and buds of walnut (Juglans regia cv 'Franquette') were measured during the rest period until bud break. This uptake capacity varies according to the temperature, the sugar and the position on the branch of the fragment studied. Between December and March, in xylem tissues, the active component of sucrose uptake was predominant compared with diffusion (90% of the total uptake), whereas the active component accounted for more moderate amounts in buds (50% of the uptake). The active uptake of hexoses took place belatedly (April) in xylem. The flow rates between xylem vessels and buds increased 1 month before bud break and reached 2000 microg sucrose h(-)(1) g DW(-)(1). Fluxes seemed to depend on bud position on the branch. However, this study strongly suggests that they were mainly dependent on the sink strength of the buds and on the sink competition between bud, xylem parenchyma and bark.

Sucrose (JrSUT1) and hexose (JrHT1 and JrHT2) transporters in walnut xylem parenchyma cells: their potential role in early events of growth resumption.

In temperate woody species, the vegetative growth period is characterized by active physiological events (e.g., bud break), which require an adequate supply of soluble sugars imported in the xylem sap stream. One-year-old shoots of walnut (Juglans regia L. cv. 'Franquette') trees, which have an acrotonic branching pattern (only apical and distal vegetative buds burst), were used to study the regulation of xylem sugar transporters in relation to bud break. At the end of April (beginning of bud break), a higher xylem sap sucrose concentration and a higher active sucrose uptake by xylem parenchyma cells were found in the apical portion (bearing buds able to burst) than in the basal portion (bearing buds unable to burst) of the sample shoots. At the same time, xylem parenchyma cells of the apical portion of the shoots exhibited greater amounts of both transcripts and proteins of JrSUT1 (Juglans regia putative sucrose transporter 1) than those of the basal stem segment. Conversely, no pronounced difference was found for putative hexose transporters JrHT1 and JrHT2 (Juglans regia hexose transporters 1 and 2). These findings demonstrate the high capacity of bursting vegetative buds to import sucrose. Immunological analysis revealed that sucrose transporters were localized in all parenchyma cells of the xylem, including vessel-associated cells, which are highly specialized in nutrient exchange. Taken together, our results indicate that xylem parenchyma sucrose transporters make a greater contribution than hexose transporters to the imported carbon supply of bursting vegetative buds.