Laboratory of Plant Gene Expression, Research Institute for Sustainable Humanosphere, Kyoto University, Uji 611-0011, Japan.
Metab Eng. 2011 Nov;13(6):629-37. doi: 10.1016/j.ymben.2011.07.003. Epub 2011 Aug 5.
Prenylated polyphenols are secondary metabolites beneficial for human health because of their various biological activities. Metabolic engineering was performed using Streptomyces and Sophora flavescens prenyltransferase genes to produce prenylated polyphenols in transgenic legume plants. Three Streptomyces genes, NphB, SCO7190, and NovQ, whose gene products have broad substrate specificity, were overexpressed in a model legume, Lotus japonicus, in the cytosol, plastids or mitochondria with modification to induce the protein localization. Two plant genes, N8DT and G6DT, from Sophora flavescens whose gene products show narrow substrate specificity were also overexpressed in Lotus japonicus. Prenylated polyphenols were undetectable in these plants; however, supplementation of a flavonoid substrate resulted in the production of prenylated polyphenols such as 7-O-geranylgenistein, 6-dimethylallylnaringenin, 6-dimethylallylgenistein, 8-dimethylallynaringenin, and 6-dimethylallylgenistein in transgenic plants. Although transformants with the native NovQ did not produce prenylated polyphenols, modification of its codon usage led to the production of 6-dimethylallylnaringenin and 6-dimethylallylgenistein in transformants following naringenin supplementation. Prenylated polyphenols were not produced in mitochondrial-targeted transformants even under substrate feeding. SCO7190 was also expressed in soybean, and dimethylallylapigenin and dimethylallyldaidzein were produced by supplementing naringenin. This study demonstrated the potential for the production of novel prenylated polyphenols in transgenic plants. In particular, the enzymatic properties of prenyltransferases seemed to be altered in transgenic plants in a host species-dependent manner.
烯丙基化多酚是有益于人类健康的次生代谢物,因为它们具有多种生物活性。利用链霉菌和苦参烯丙基转移酶基因通过代谢工程在转基因豆科植物中产生烯丙基化多酚。三个链霉菌基因,NphB、SCO7190 和 NovQ,其基因产物具有广泛的底物特异性,在模式豆科植物百脉根中过表达,通过修饰来诱导蛋白质定位,分别在细胞质、质体或线粒体中过表达。两个来自苦参的植物基因,N8DT 和 G6DT,其基因产物显示出狭窄的底物特异性,也在百脉根中过表达。这些植物中检测不到烯丙基化多酚;然而,添加黄酮类底物会导致产生烯丙基化多酚,如 7-O-香叶基染料木黄酮、6-二甲基烯丙基柚皮素、6-二甲基烯丙基染料木黄酮、8-二甲基烯丙基柚皮素和 6-二甲基烯丙基染料木黄酮在转基因植物中。尽管具有天然 NovQ 的转化体没有产生烯丙基化多酚,但修饰其密码子使用会导致在添加柚皮素后转化体产生 6-二甲基烯丙基柚皮素和 6-二甲基烯丙基染料木黄酮。即使在底物喂养下,线粒体靶向转化体也不会产生烯丙基化多酚。SCO7190 也在大豆中表达,并通过补充柚皮素产生二甲烯丙基芹黄素和二甲烯丙基大豆苷元。本研究证明了在转基因植物中生产新型烯丙基化多酚的潜力。特别是,烯丙基转移酶的酶学特性似乎以宿主物种依赖的方式在转基因植物中发生改变。