Gorlaeus Laboratories, Pharmacognosy Department/Metabolomics, Institute of Biology Leiden, Leiden University, Leiden The Netherlands.
Genet Mol Biol. 2010 Oct;33(4):703-13. doi: 10.1590/S1415-47572010005000088. Epub 2010 Dec 1.
Cannabinoids, flavonoids, and stilbenoids have been identified in the annual dioecious plant Cannabis sativa L. Of these, the cannabinoids are the best known group of this plant's natural products. Polyketide synthases (PKSs) are responsible for the biosynthesis of diverse secondary metabolites, including flavonoids and stilbenoids. Biosynthetically, the cannabinoids are polyketide substituted with terpenoid moiety. Using an RT-PCR homology search, PKS cDNAs were isolated from cannabis plants. The deduced amino acid sequences showed 51%-73% identity to other CHS/STS type sequences of the PKS family. Further, phylogenetic analysis revealed that these PKS cDNAs grouped with other non-chalcone-producing PKSs. Homology modeling analysis of these cannabis PKSs predicts a 3D overall fold, similar to alfalfa CHS2, with small steric differences on the residues that shape the active site of the cannabis PKSs.
在一年生雌雄异株植物大麻(Cannabis sativa L.)中已经鉴定出大麻素、类黄酮和芪类化合物。在这些化合物中,大麻素是这种植物天然产物中最著名的一类。聚酮合酶(PKSs)负责多种次生代谢物的生物合成,包括类黄酮和芪类化合物。生物合成上,大麻素是由萜烯部分取代的聚酮化合物。通过 RT-PCR 同源搜索,从大麻植物中分离出 PKS cDNA。推导的氨基酸序列与 PKS 家族的其他 CHS/STS 型序列具有 51%-73%的同一性。此外,系统发育分析表明,这些 PKS cDNA 与其他非查耳酮产生的 PKS 聚在一起。这些大麻 PKS 的同源建模分析预测了一个 3D 整体折叠,类似于紫花苜蓿 CHS2,在塑造大麻 PKS 活性位点的残基上存在小的空间差异。