Abstract
以苎麻[ Boehmeria nivea (L.) Gaud]中苎1号为材料，采用简并RT-PCR法、RACE技术以及全长cDNA文库筛选，克隆苎麻果胶主要多糖组分的合成关键酶 UGlcAE cDNA序列，序列长度为1 257 bp，编码区长723 bp，可编码241个氨基酸序列。实时定量PCR证实， UGlcAE 表达量为根部＞叶片＞韧皮部＞木质部，在根部的表达量占优势。该结果对我们后期采用分子生物学方法来调控果胶的合成量具有实际意义。
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