Growth Substrate and Nutrient Salt Environment Alter Mannitol-to-Hexose Partitioning in Celery Petioles

Abstract

The fleshy parenchyma tissue of celery [Apium graveolens L. var. dulce (Mill.) Pers.] petioles is the major storage tissue for the sugar alcohol mannitol and for the hexoses, glucose and fructose. In this study, we found that plants grown in the soilless mixture, Promix, fertilized weekly with a nutrient solution, or grown in a hydroponic container culture, differed in carbohydrate composition. However, plant growth was not affected. Higher mannitol and lower hexose concentrations were present in petioles from plants grown hydroponically. This was true in petioles that did not differ in total soluble carbohydrate concentration. The ratio of mannitol to hexose concentration in petioles was ≈2-fold higher for hydroponically grown plants compared to Promix-grown plants, and the higher ratio was maintained during the entire 12-week experimental period. Carbohydrate partitioning was also affected by petiole development within the plant. Sucrose and hexose concentrations were highest in mature petioles, whereas mannitol was relatively high in all petioles except the oldest ones. Because the mineral solution applied to the Promix-grown plants had a lower total salt concentration compared to hydroponically grown plants, we postulated that the salt concentration of the mineral solution might be an important factor affecting C partitioning in celery petioles. When plants were grown hydroponically at two different salt concentrations [electrical conductivity (EC) = 2.7 and 6.0 mS·cm-1], high mannitol-to-hexose ratios were observed in celery petioles of plants grown at high salt concentration (EC = 6.0 mS·cm-1), a result supporting the hypothesis that the salt environment might alter mannitol and hexose concentrations in a coordinated way. These data are consistent with the hypothesis that elevated mannitol levels may be a significant component of plant adjustment to salt stress, possibly adding osmotic adjustment and preventing inactivation of metabolic processes.