The fate of apoplastic sucrose in sink and source leaves of Urtica dioica

Abstract

Experiments were performed with developing and mature leaves of Urtica dioica L. to trace differences which could be interpreted in terms of cell wall‐bound acid invertase (EC 3.2.1.26) participating in phloem unloading in a sink leaf. The pH of apoplastic fluid that was collected by gentle centrifugation of entire leaves was identical (7.1) in the two types of leaves; also, fluorometric determination with esculetin showed a neutral apoplastic pH between 7.0 in the source and 7.2 in the sink leaf. To detect whether differences in apoplastic pH occur within limited leaf areas, such as of the tissue surrounding the veins, the metabolic fate of [14C]–(fructosyl)‐sucrose that was administered via the xylem was investigated. In source leaves, there was a large transitory decrease in [14C]‐sucrose followed by a substantial resynthesis of this compound. In sink leaves, resynthesis was less significant and carbon was incorporated mainly in starch, charged soluble compounds and cell walls. However, after correction for resynthesis, the two types of leaves showed an identical capacity for sucrose cleavage. Finally, activation of the apoplastic invertase by administering labelled sucrose in buffered solution of pH 5.0 did not result in an enhanced degradation. By contrast, apoplastic fluid collected from leaves which had been infiltrated with buffer solutions of pH 5.5 and 8.0, respectively, showed a rapid adjustment of the pH close to the natural neutral value by the mesophyll tissue. The results are incompatible with the idea of an active invertase in the sink (and the source) leaves apoplast, and hence do not lend support to the theory of apoplastic cleavage of sucrose being required for phloem unloading in this kind of a utilization sink.

The Morphogenic Response of Plants to Soil Nitrogen: Adaptive Regulation of Biomass Distribution and Nitrogen Metabolism by Phytohormones

“…The apoplastic pH measured in both types of leaves ranged between 7.0 and 7.2 and therefore is unfavorable to the acid cell wall invertase (Moller and Beck, 1992). The apoplastic pH measured in both types of leaves ranged between 7.0 and 7.2 and therefore is unfavorable to the acid cell wall invertase (Moller and Beck, 1992).…”