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机构地区:[1]厦门大学生物学系
出 处:《厦门大学学报(自然科学版)》1993年第5期634-640,共7页Journal of Xiamen University:Natural Science
基 金:国家自然科学基金
摘 要:经硫酸铵分级、DEAE-纤维素和葡聚糖凝胶柱层析,叶中UDPG PPLase被纯化166倍,该酶最适反应温度32℃,最佳反应pH8.0.2mmol/L的Ca^(2+)和5mmol/L的Mg^(2+)对该酶有较好激活效果,但无绝对依赖关系,Pb^(2+)对该酶有较强抑制作用,亚细胞分级分离结果表明95%的UDPG PPLase活性分布于46000×980cm /s^2上清液;电镜细胞化学定位研究表明,该酶主要定位于液泡、高尔基扁平囊和高尔基小泡;还讨论该酶在甜菊糖甙生物合成中的作用。By means of ammonium sulfate fraction, and column chromatography on DEAE-Cellulose and Sephadex, UDPG PPLase was purified 166 folds. The optimal tempera-ture for the reaction of the enzyme was 32℃, the optimal pH was 8. 0. 2m mol/l Ca2+ and 5 mmol/1 Mg2+ was a good activative element for UDPG PPLase, but not an absolutely needed condition. Pb2+ showed strong inhibition. The result of subcellular fraction indicated that 95% of UDPG PPLase activity was distributed in the superatant of 46 000×980 cm/s2. The observation of electron microscopic cytochemistry demonstrated that UDPG PPLase was largely located in the vaeuloes, golgi body and golgi vesides. The role of UDPG PPLase in cell steviol-gtacosides biosythesis was also discussed.
分 类 号:Q949.783.5[生物学—植物学]
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