2.4.1.13	abscisic acid	as well as treatments like spikelet thinning, leaf cutting increase enzyme expression and enzyme activity during rice grain filling	704879	
2.4.1.13	actin	activity of SuSy2 in breakdown direction is stimulated by 60%	660272	
2.4.1.13	allantoin	activation, sucrose synthesis	488555	
2.4.1.13	Ca2+	only for sucrose synthesis	488577	
2.4.1.13	fructose 2,6-bisphosphate	stimulates SuSy2 in presence of actin	660272	
2.4.1.13	Mg2+	2-4fold activation of sucrose synthesis, not cleavage	488567	
2.4.1.13	Mg2+	only for sucrose synthesis	488577	
2.4.1.13	Mn2+	2-4fold activation of sucrose synthesis, inhibition of cleavage	488567	
2.4.1.13	additional information	increase of enzyme activity in synthezising direction in leaves during fruit development, increase of enzyme activity in synthezising and in degrading direction in mesocarp tissue during fruit development	706750	
2.4.1.13	additional information	peak of activities at the 21th day post anthesis, higher activity in the cultivar with a high starch content	706742	
2.4.1.13	additional information	when suffering hypoxia stress from flooding, CsSUS3 expression and SUS activity in roots increase, especially in the lateral roots. The soluble SUS activity increases, but the membrane fraction hardly changes	736966	
2.4.1.13	nitrate	50% activation at 3-5 mM, exogenous nitrate at 14.2 mM absorbed in the form of KNO3 and Ca(NO3)2 during 10-20 days exponentially activates the enzyme in the roots by 22-100% as compared with plants grown on nitrogen-free medium. Under low light, nitrate can not activate sucrose synthase	706740	
2.4.1.13	NO3	20.8% increase of activity at 2 mM	757316	
2.4.1.13	spermine	0.07 mM spermine treatment significantly increases the enzyme activity at 15 and 35 days after post anthesis	757492	
2.4.1.13	sucrose	exogenous, as well as treatments like spikelet thinning, leaf cutting increase enzyme expression and enzyme activity during rice grain filling	704879	
2.4.1.13	UDP-D-xylose	activation of epicotyl and cotyledon isozymes	488543