首页 | 本学科首页   官方微博 | 高级检索  
   检索      


Stimulation of sugar exit from leaf tissues ofVicia faba L.
Authors:Bertrand M'Batchi  Serge Delrot
Institution:(1) Station Biologique de Beau-Site, ERA 701, CNRS, Université de Poitiers, 25 rue du Faubourg St-Cyprien, F-86000 Poitiers, France
Abstract:After removal of the lower epidermis, leaf discs ofVicia faba L. were loaded with either 14C]sucrose or 3H]3-O-methylglucose (3-O-MeG). The exit of preloaded sucrose was strongly stimulated when sucrose was present in the bathing medium, and the exit of 3-O-MeG was also markedly increased in the presence of 3-O-MeG. This specific stimulation exhibited single saturation dependence on the external concentration of sugar (K m=9 mM for sucrose, 5 mM for 3-O-MeG), and was sensitive to low temperature, uncouplers and thiol reagents. Sucrose exit was never affected by 3-O-MeG in the bathing medium. Sucrose did not affect the exit of 3-O-MeG in fresh discs, but promoted this exit in discs previously aged for 12 h, indicating partial external hydrolysis of sucrose in the latter tissues. Ageing also dramatically increased the exit of 3-O-MeG induced by 3-O-MeG but had no effect on the exit of sucrose induced by sucrose. The ability of 53 compounds (pentoses, hexoses, hexose-phosphates, polyols, di- and trisaccharides, phenyl- and nitrophenyl-derivatives, sweeteners) to interact with the sucrose carrier and with the hexose carrier was tested. Sucrose, maltose, agr-phenylglucoside andp-nitrophenyl-agr-glucoside interacted with the sucrose carrier.d-glucose,d-xylose,d-fucose,d-galactose,d-mannose, 3-O-MeG and 2-deoxyglucose interacted with the hexose carrier.Abbreviations CCCP carbonylcyanide-m-chlorophenylhydrazone - EGTA ethylene glycol-bis(beta-aminoethyl ether)-N,N,Nprime,Nprime-tetraacetic acid - 3-O-MeG 3-O-methylglucose - PCMBS p-chloromercuribenzenesulphonic acid
Keywords:Carrier specificity  Hexose transport  Leaf (sugar transport)  Membrane (sugar transport)  Sucrose transport  Vicia (sugar transport)
本文献已被 SpringerLink 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号