Mercke P, Crock J, Croteau R, Brodelius P E
Department of Plant Biochemistry, Lund University, Lund, S-22100, Sweden.
Arch Biochem Biophys. 1999 Sep 15;369(2):213-22. doi: 10.1006/abbi.1999.1358.
Sesquiterpene cyclases (synthases) catalyze the conversion of the isoprenoid intermediate farnesyl diphosphate to various sesquiterpene structural types. In plants, many sesquiterpenes are produced as defensive chemicals (phytoalexins) or mediators of chemical communication (i.e., pollinator attractants). A number of sesquiterpene synthases are present in Artemisia annua L. (annual wormwood). We have isolated a cDNA clone encoding one of these, epi-cedrol synthase. This clone contains a 1641-bp open reading frame coding for 547 amino acids (63.5 kDa), a 38-bp 5'-untranslated end, and a 272-bp 3'-untranslated sequence. The deduced amino acid sequence was 32 to 43% identical with the sequences of other known sesquiterpene cyclases from angiosperms. When expressed in Escherichia coli, the recombinant enzyme catalyzed the formation of both olefinic (3%) and oxygenated (97%) sesquiterpenes from farnesyl diphosphate. GC-MS analysis identified the olefins as alpha-cedrene (57% of the olefins), beta-cedrene (13%), (E)-beta-farnesene (5%), alpha-acoradiene (1%), (E)-alpha-bisabolene (8%), and three unknown olefins (16%) and the oxygenated sesquiterpenes (97% of total sesquiterpene generated, exclusive of farnesol and nerolidol) as cedrol (4%) and epi-cedrol (96%). epi-Cedrol synthase was not active with geranylgeranyl diphosphate as substrate, whereas geranyl diphosphate was converted to monoterpenes by the recombinant enzyme at a rate of about 15% of that observed with farnesyl diphosphate as substrate. The monoterpene olefin products are limonene (45%), terpinolene (42%), gamma-terpinene (8%), myrcene (5%), and alpha-terpinene (2%); a small amount of the monoterpene alcohol terpinen-4-ol is also produced. The pH optimum for the recombinant enzyme is 8.5-9.0 (with farnesyl diphosphate as substrate) and the K(m) values for farnesyl diphosphate are 0.4 and 1.3 microM at pH 7. 0 and 9.0, respectively. The K(m) for Mg(2+) is 80 microM at pH 7.0 and 9.0.
倍半萜环化酶(合酶)催化类异戊二烯中间体法呢基二磷酸转化为各种倍半萜结构类型。在植物中,许多倍半萜作为防御性化学物质(植保素)或化学通讯介质(即传粉者引诱剂)产生。黄花蒿(一年生艾草)中存在多种倍半萜合酶。我们分离出了一个编码其中一种酶——表柏木醇合酶的cDNA克隆。该克隆包含一个1641 bp的开放阅读框,编码547个氨基酸(63.5 kDa)、一个38 bp的5'非翻译末端和一个272 bp的3'非翻译序列。推导的氨基酸序列与来自被子植物的其他已知倍半萜环化酶序列的同一性为32%至43%。当在大肠杆菌中表达时,重组酶催化法呢基二磷酸形成烯烃类(3%)和氧化型(97%)倍半萜。气相色谱-质谱分析确定烯烃为α-雪松烯(占烯烃的57%)、β-雪松烯(13%)、(E)-β-法呢烯(5%)、α-菖蒲二烯(1%)、(E)-α-红没药烯(8%)和三种未知烯烃(16%),氧化型倍半萜(占生成的总倍半萜的97%,不包括法呢醇和橙花叔醇)为柏木醇(4%)和表柏木醇(96%)。表柏木醇合酶以香叶基香叶基二磷酸为底物时无活性,而重组酶将香叶基二磷酸转化为单萜的速率约为以法呢基二磷酸为底物时观察到的速率的15%。单萜烯烃产物为柠檬烯(45%)、萜品油烯(42%)、γ-萜品烯(8%)、月桂烯(5%)和α-萜品烯(2%);还产生少量的单萜醇萜品-4-醇。重组酶的最适pH为8.5 - 9.0(以法呢基二磷酸为底物),在pH 7.0和9.0时,法呢基二磷酸的K(m)值分别为0.4和1.3 μM。Mg(2+)在pH 7.0和9.0时的K(m)为80 μM。