Title of article
Sucrose synthase isoforms in cultured tobacco cells
Author/Authors
Matic، نويسنده , , Sandra and إkerlund، نويسنده , , Hans-Erik and Everitt، نويسنده , , Einar and Widell، نويسنده , , Susanne، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2004
Pages
8
From page
299
To page
306
Abstract
The plant enzyme sucrose synthase (SuSy; EC 2.4.1.13) catalyzes the reversible conversion of sucrose and UDP into UDP-glucose (UDP-Glc) and fructose. The enzyme exists in different isoforms and is both located in the cytosol, membrane-bound and associated to the actin cytoskeleton. We here investigate sucrose synthase from tobacco (Nicotiana tabacum L.) BY-2 heterotrophic cell suspensions. Two different isoforms of sucrose synthase SuSy1 and SuSy2, could be purified from cytosolic extracts of these cells using a combination of poly(ethylene glycol) (PEG) precipitation, gel filtration, ion-exchange chromatography and affinity chromatography. They were clearly distinct, both with regard to the binding to the ion-exchange column and with regard to their kinetic and regulatory properties. SuSy1, the more abundant species, showed lower Vmax and Km for sucrose and UDP compared to the less abundant SuSy2. The activity of SuSy2 in the breakdown direction was stimulated by 60% by actin, in contrast to that of SuSy1, which showed a 17% inhibition. An indication of interaction between SuSy1 and actin was obtained by partitioning in aqueous Dextran–PEG two-phase systems. Furthermore, fructose 2,6-bisphosphate (F26BP) at micromolar concentrations stimulated SuSy2 in the presence of actin while SuSy1 was strongly inhibited by fructose. Possible roles of these two isoforms in the sucrose turnover in BY-2 cells are discussed.
Keywords
Two-phase partitioning , Actin , BY-2 cells , 6-bisphosphate , Sucrolysis , sucrose synthase , fructose 2 , Tobacco
Journal title
Plant Physiology and Biochemistry
Serial Year
2004
Journal title
Plant Physiology and Biochemistry
Record number
2120922
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