Department of Botany, University of California, Berkeley, California 94720.
Plant Physiol. 1979 Dec;64(6):909-13. doi: 10.1104/pp.64.6.909.
The peripheral root cap cells of corn (cv. SX-17A) secrete a fucose-rich, high molecular weight, polysaccharide slime via the dictyosome pathway. To study the synthesis of this polysaccharide, a technique for isolating and assaying GDP-fucose:polysaccharide fucosyl transferase activity was developed. Corn roots were excised from germinated seeds, incubated 12 hours at 10 C in water, and ground in 100 millimolar Tris or Pipes buffer (pH 7.0) with or without 0.5 molar sucrose. The membrane-bound enzyme was solubilized by sonication in the presence of 2 molar urea and 1.5% (v/v) Triton X-100 and assayed by monitoring the incorporation of GDP-[(14)C]fucose into endogenous acceptors. Optimum enzyme activity is expressed at pH 7.0 and 30 C in the presence of 0.8% (v/v) Triton X-100. The enzyme does not require divalent cations for activation and is inhibited by concentrations of MnCl(2) or MgCl(2) greater than 1 millimolar. Corn root cap slime will serve as an exogenous acceptor for the enzyme if it is first hydrolyzed in 5 millimolar trifluoroacetic acid for 60 minutes at 18 pounds per square inch, 121 C. This procedure prepares the acceptor by removing terminal fucose residues from the slime molecule. Kinetics of fucose release during hydrolysis of native slime and in vitro synthesized product suggests that the two polymers possess similar linkages to fucose.
玉米(品种 SX-17A)外周根冠细胞通过高尔基复合体途径分泌富含岩藻糖、高分子量的多糖粘液。为了研究这种多糖的合成,开发了一种分离和测定 GDP-岩藻糖:多糖岩藻糖基转移酶活性的技术。从发芽种子中切取玉米根,在 10°C 的水中孵育 12 小时,然后在含有或不含有 0.5 摩尔蔗糖的 100 毫摩尔 Tris 或 Pipes 缓冲液(pH 7.0)中研磨。在 2 摩尔尿素和 1.5%(v/v)Triton X-100 的存在下通过超声处理使膜结合酶溶解,并通过监测 GDP-[14C]岩藻糖掺入内源性受体来测定酶活性。在 pH 7.0 和 30°C 的条件下,在 0.8%(v/v)Triton X-100 的存在下,酶的活性最佳。该酶不需要二价阳离子激活,并且被浓度大于 1 毫摩尔的 MnCl2 或 MgCl2 抑制。如果玉米根冠粘液首先在 5 毫摩尔三氟乙酸中于 18 磅/平方英寸、121°C 下水解 60 分钟,则可以作为酶的外源性受体。该程序通过从粘液分子中去除末端岩藻糖残基来制备受体。在天然粘液和体外合成产物的水解过程中释放岩藻糖的动力学表明,这两种聚合物与岩藻糖具有相似的键合。