ABSTRACTpropose that they should be more correctly termed sucrolysis and sucroneogenesis. Before recent work it was customary to assume that sucrose synthase action resulted in the formation of UDP-glucose and then other nucleotide sugars leading into sugar polymer synthesis, such as plant cell walls. However, a substrate level pool of PPi was measured in plants (2,7,27), and we successfully tested the pyrophosphorolysis of UDPglucose feeding glucose 1-P directly into plant metabolism (32). These steps are an integral part of the recently proposed sucrose synthase pathway (1,15,30). Then, of course, from glycolysis carbon can be directed into essentially every metabolic activity of a cell. Therefore, the ability of a tissue or organ to metabolize sucrose must be one determinant of sink strength. Here we have tested the feasibility of biochemically measuring sucrose sink strength by assaying sucrose cleavage activities, i.e. sucrolysis via either the invertases or by the sucrose synthase pathway. The reasons we developed this UDP and PPi-dependent assay for sucrose synthase activity were (a) to measure activity in the sucrose breakdown direction whereas many other workers measured the opposite, namely sucrose synthesis (3,4,22,26), and (b) others who measured sucrose breakdown often assayed for UDP-glucose accumulation as a precursor of the synthesis of cell walls or other nucleotide sugars (6, 22). But in our assay we couple through the PPi-dependent UDP-glucopyrophosphorylase, which is very active in plants, to the formation of glucose 1-P which feeds carbon directly into glycolysis and possibly on to starch formation (31,32