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Kinetin-induced caffeic acid O-methyltransferases in cell suspension cultures of Vanilla planifolia Andr. and isolation of caffeic acid O-methyltransferase cDNAs

机译:香草平坦叶植物Andr。细胞悬浮培养物中激动素诱导的咖啡酸O-甲基转移酶酸O-甲基转移酶cDNA的克隆与分离

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Two S-adenosyl-L-methionine:caffeic acid methyltransferases were induced in kinetin-treated cell cultures of Vanilla planifolia. Upon addition of kinetin to the culture, maximum activities of caffeic acid 4-O-methyltransferase and caffeic acid 3-O-methyltransferase were obtained after about 2 and 40 h, respectively. The former enzyme is involved in the biosynthesis of vanillic acid and the latter enzyme is co-induced with other enzymes of the general phenylpropanoid pathway and is involved in the biosynthesis of lignin precursors. A number of cDNA clones encoding S-adenosyl-L-methionine:caffeic acid-methyltransferases were isolated by heterologous probe screening of a lambdaZapII cDNA library constructed from mRNA of a kinetin-treated cell suspension culture of V. planifolia. A full-length cDNA clone, Vpomt35, contained a 1089-bp open reading frame coding for 363 amino acid residues, a 25-bp 5'-end sequence and a 214-bp 3'-end non-coding sequence. The deduced amino acid sequence of Vpomt35 revealed 56 to 80% sequence identity when compared with those of other plant caffeic acid O-methyltransferases. Detection of methyltransferase activity in extracts of Escherichia coli XL-1 Blue cells transformed with a pBluescript phagemid construct containingVpomt35 confirmed that this cDNA clone encodes a caffeic acid 3-O-methyltransferase. The enzyme also exhibits a low caffeic acid 4-O-methyltransferase activity (2% of the caffeic acid 3-O-methyltransferase activity). A number of other cDNA clones encoding caffeic acid O-methyltransferases were also sequenced. Comparison of nucleotide and deduced amino acid sequences of these cDNAs indicated two types of caffeic acid O-methyltransferase cDNAs which showed 94% sequence identity in the coding region, butonly 55% homology with several gaps in the 3' untranslated end. Results from Southern blot analysis suggested that the caffeic acid O-methyltransferase gene is organized as a small family with at least two genes, which are expressed in V. planifolia cellsuspension cultures.
机译:两种S-腺苷-L-蛋氨酸:咖啡酸甲基转移酶在经香草素处理过的香草叶的细胞培养物中被诱导。在将动蛋白添加到培养物中后,分别在约2 h和40 h后获得了咖啡酸4-O-甲基转移酶和咖啡酸3-O-甲基转移酶的最大活性。前一种酶参与香草酸的生物合成,而后一种酶与一般苯丙烷类途径的其他酶共同诱导,并参与木质素前体的生物合成。通过异源探针筛选从lambdaZapII cDNA文库中分离出许多编码S-腺苷-L-甲硫氨酸:咖啡酸-甲基转移酶的cDNA克隆,该文库由经动蛋白处理过的葡萄球菌悬浮细胞培养物的mRNA构建而成。全长cDNA克隆Vpomt35包含一个1089 bp的开放阅读框,编码363个氨基酸残基,25 bp的5'端序列和214 bp的3'端非编码序列。与其他植物咖啡酸O-甲基转移酶相比,Vpomt35推导的氨基酸序列显示出56%至80%的序列同一性。在用含有Vpomt35的pBluescript噬菌粒构建体转化的大肠杆菌XL-1 Blue细胞提取物中检测甲基转移酶活性,证实此cDNA克隆编码咖啡酸3-O-甲基转移酶。该酶还显示出低咖啡酸4-O-甲基转移酶活性(占咖啡酸3-O-甲基转移酶活性的2%)。还对许多其他编码咖啡酸O-甲基转移酶的cDNA克隆进行了测序。这些cDNA的核苷酸序列和推导的氨基酸序列的比较表明,两种类型的咖啡酸O-甲基转移酶cDNA在编码区显示94%的序列同一性,但在3′非翻译末端仅具有55%的同源性和几个缺口。 Southern印迹分析的结果表明,咖啡酸O-甲基转移酶基因是一个由至少两个基因组成的小家族,它们在V. Planifolia细胞悬浮培养物中表达。

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