Qin Ping, Chen Peng, Zhou Yuanwei, Zhang Wei, Zhang Yunyun, Xu Jingjing, Gan Lu, Liu Yingnan, Romer Jill, Dörmann Peter, Cahoon Edgar B, Zhang Chunyu
National Key Laboratory of Crop Genetic Improvement and College of Plant Science and Technology, Huazhong Agricultural University, Wuhan, China.
Yichang Academy of Agricultural Science, Ministry of Agriculture and rural areas, Yichang, Hubei, China.
Front Plant Sci. 2024 Feb 26;15:1344095. doi: 10.3389/fpls.2024.1344095. eCollection 2024.
Homogentisate Phytyltransferase () catalyzes condensation of homogentisate (HGA) and phytyl diphosphate (PDP) to produce tocopherols, but can also synthesize tocotrienols using geranylgeranyl diphosphate (GGDP) in plants engineered for deregulated HGA synthesis. In contrast to prior tocotrienol biofortification efforts, engineering enhanced tocopherol concentrations in green oilseeds has proven more challenging due to the integral role of chlorophyll metabolism in supplying the PDP substrate. This study show that RNAi suppression of coupled with overexpression increases tocopherol concentrations by >two-fold in Arabidopsis seeds. We obtained additional increases in seed tocopherol concentrations by engineering increased HGA production via overexpression of bacterial that encodes chorismate mutase/prephenate dehydrogenase activities. In overexpression lines, seed tocopherol concentrations increased nearly three-fold, and resulted in modest tocotrienol accumulation. We further increased total tocochromanol concentrations by enhancing production of HGA and GGDP by overexpression of the gene for hydroxyphenylpyruvate dioxygenase (HPPD). This shifted metabolism towards increased amounts of tocotrienols relative to tocopherols, which was reflected in corresponding increases in ratios of GGDP/PDP in these seeds. Overall, our results provide a theoretical basis for genetic improvement of total tocopherol concentrations in green oilseeds (e.g., rapeseed, soybean) through strategies that include seed-suppression of coupled with increased HGA production.
尿黑酸植基转移酶()催化尿黑酸(HGA)与植基二磷酸(PDP)缩合生成生育酚,但在经过工程改造以解除HGA合成调控的植物中,该酶也能利用香叶基香叶基二磷酸(GGDP)合成生育三烯酚。与之前的生育三烯酚生物强化努力不同,由于叶绿素代谢在提供PDP底物方面的不可或缺作用,在绿色油料种子中工程化提高生育酚浓度已被证明更具挑战性。本研究表明,对的RNA干扰抑制与的过表达相结合,可使拟南芥种子中的生育酚浓度提高两倍以上。通过对编码分支酸变位酶/预苯酸脱氢酶活性的细菌的过表达来工程化增加HGA的产生,我们进一步提高了种子中的生育酚浓度。在过表达株系中,种子生育酚浓度增加了近三倍,并导致了适度的生育三烯酚积累。我们通过过表达对羟基苯丙酮酸双加氧酶(HPPD)基因来增强HGA和GGDP的产生,进一步提高了总生育三烯酚浓度。这使代谢朝着相对于生育酚增加生育三烯酚的量转变,这反映在这些种子中GGDP/PDP比值的相应增加上。总体而言,我们的结果为通过包括对进行种子抑制并增加HGA产生在内的策略,对绿色油料种子(如油菜籽、大豆)中的总生育酚浓度进行遗传改良提供了理论基础。