Lingnan Medical Research Center, Guangzhou University of Chinese Medicine, 12 Jichang Rd, Guangzhou 510405, China.
The First Clinical Medical School, Guangzhou University of Chinese Medicine, Guangzhou 510405, China.
Plant Cell Physiol. 2021 Nov 17;62(9):1423-1435. doi: 10.1093/pcp/pcab089.
Isodon lophanthoides var. gerardiana (Lamiaceae), also named xihuangcao, is a traditional Chinese medicinal herb that exhibits a broad range of pharmacological activities. Abietane-type diterpenoids are the characteristic constituents of I. lophanthoides, yet their biosynthesis has not been elucidated. Although the aerial parts are the most commonly used organs of I. lophanthoides, metabolite profiling by gas chromatography-mass spectrometry showed the underground parts also contain large amounts of labdane diterpenoids including abietatriene, miltiradiene and ferruginol, which are distinct from the 13-hydroxy-8(14)-abietene detected in the aerial parts. Comparative transcriptome analysis of root and leaf samples identified a diverse diterpene synthase family including 6 copalyl diphosphate synthase (IlCPS1-6) and 5 kaurene synthase-like (IlKSL1-5). Here we report the functional characterization of six of these enzymes using yeast heterologous expression system. Both IlCPS1 and IlCPS3 synthesized (+)-copalyl diphosphate (CPP), in combination with IlKSL1 resulted in miltiradiene, precursor of abietane-type diterpenoids, while coupling with IlKSL5 led to the formation of hydroxylated diterpene scaffold nezukol. Expression profiling and phylogenetic analysis further support the distinct evolutionary relationship and spatial distribution of IlCPS1 and IlCPS3. IlCPS2 converted GGPP into labda-7,13E-dien-15-ol diphosphate. IlCPS6 was identified as ent-CPS, indicating a role in gibberellin metabolism. We further identified a single residue that determined the water addition of nezukol synthase IlKSL5. Substitution of alanine 513 with isoleucine completely altered the product outcome from hydroxylated nezukol to isopimara-7,15-diene. Together, these findings elucidated the early steps of bioactive abietane-type diterpenoid biosynthesis in I. lophanthoides and the catalytic mechanism of nezukol synthase.
香茶菜属植物 Isodon lophanthoides var. gerardiana(唇形科),又名溪黄草,是一种具有广泛药理活性的传统中药。贝壳杉烷型二萜类化合物是 I. lophanthoides 的特征成分,但它们的生物合成尚未阐明。尽管地上部分是 I. lophanthoides 最常用的器官,但气相色谱-质谱联用仪的代谢物分析表明,地下部分也含有大量的贝壳杉烷二萜类化合物,包括 abietatriene、miltiradiene 和 ferruginol,与在地上部分检测到的 13-羟基-8(14)-abietene 不同。根和叶样本的比较转录组分析鉴定了一个多样化的二萜合酶家族,包括 6 个焦磷酸香叶酯合酶(IlCPS1-6)和 5 个贝壳杉烯合酶样(IlKSL1-5)。在这里,我们使用酵母异源表达系统报告了其中 6 种酶的功能特征。IlCPS1 和 IlCPS3 均能合成(+)-焦磷酸香叶酯(CPP),与 IlKSL1 结合可合成贝壳杉烷型二萜前体 miltiradiene,与 IlKSL5 结合可形成羟基化二萜骨架 nezukol。表达谱分析和系统发育分析进一步支持了 IlCPS1 和 IlCPS3 的独特进化关系和空间分布。IlCPS2 将 GGPP 转化为 labda-7,13E-dien-15-ol 二磷酸。IlCPS6 被鉴定为 ent-CPS,表明其在赤霉素代谢中起作用。我们进一步鉴定了一个单一残基,该残基决定了 nezukol 合酶 IlKSL5 的水添加。将 513 位丙氨酸突变为异亮氨酸完全改变了产物结果,从羟基化的 nezukol 转变为异佛尔酮-7,15-二烯。总之,这些发现阐明了 I. lophanthoides 中生物活性贝壳杉烷型二萜生物合成的早期步骤以及 nezukol 合酶的催化机制。