Liu Xiaoqiang, Xiang Min, Fan Yufang, Yang Chunxian, Zeng Lingjiang, Zhang Qitang, Chen Min, Liao Zhihua
Key Laboratory of Eco-environments in Three Gorges Reservoir Region - Ministry of Education, Chongqing Engineering Research Centre for Sweet Potato, School of Life Sciences, Southwest University Chongqing, China.
College of Pharmaceutical Sciences, Southwest University Chongqing, China.
Front Plant Sci. 2017 Feb 28;8:279. doi: 10.3389/fpls.2017.00279. eCollection 2017.
Purple-fleshed sweet potato is good for health due to rich anthocyanins in tubers. Although the anthocyanin biosynthetic pathway is well understood in up-ground organs of plants, the knowledge on anthocyanin biosynthesis in underground tubers is limited. In the present study, we isolated and functionally characterized a root-preferential gene encoding dihydrokaempferol reductase () from purple-fleshed sweet potato. IbDHKR showed highly similarity with the reported dihydroflavonol reductases in other plant species at the sequence levels and the NADPH-binding motif and the substrate-binding domain were also found in IbDHKR. The tissue profile showed that was expressed in all the tested organs, but with much higher level in tuber roots. The expression level of was consistent with the anthocyanin content in sweet potato organs, suggesting that tuber roots were the main organs to synthesize anthocyanins. The recombinant 44 kD IbDHKR was purified and fed by three different dihydroflavonol substrates including dihydrokaempferol (DHK), dihydroquerctin, and dihydromyrecetin. The substrate feeding assay indicated that only DHK could be accepted as substrate by IbDHKR, which was reduced to leucopelargonidin confirmed by LC-MS. Finally, IbDHKR was overexpressed in transgenic tobacco. The IbDHKR-overexpression tobacco corolla was more highly pigmented and contained higher level of anthocyanins than the wild-type tobacco corolla. In summary, was a root-preferential gene involved in anthocyanin biosynthesis and its encoding protein, specifically catalyzing DHK reduction to yield leucopelargonidin, was a candidate gene for engineering anthocyanin biosynthetic pathway.
紫肉甘薯因块茎中富含花青素而有益健康。尽管花青素生物合成途径在植物地上器官中已被充分了解,但关于地下块茎中花青素生物合成的知识却很有限。在本研究中,我们从紫肉甘薯中分离出一个根优先表达的编码二氢山奈酚还原酶()的基因,并对其进行了功能鉴定。IbDHKR在序列水平上与其他植物物种中报道的二氢黄酮醇还原酶高度相似,并且在IbDHKR中也发现了NADPH结合基序和底物结合结构域。组织表达谱显示,该基因在所有测试器官中均有表达,但在块根中的表达水平要高得多。该基因的表达水平与甘薯器官中的花青素含量一致,表明块根是合成花青素的主要器官。重组的44 kD IbDHKR被纯化,并以三种不同的二氢黄酮醇底物进行饲喂,包括二氢山奈酚(DHK)、二氢槲皮素和二氢杨梅素。底物饲喂试验表明,只有DHK可以被IbDHKR接受为底物,通过液相色谱-质谱联用仪确认其被还原为无色天竺葵素。最后,IbDHKR在转基因烟草中过表达。与野生型烟草花冠相比,过表达IbDHKR的烟草花冠色素沉着更高,花青素含量也更高。总之,该基因是参与花青素生物合成的根优先表达基因,其编码的蛋白特异性催化DHK还原生成无色天竺葵素,是工程改造花青素生物合成途径的候选基因。