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A Root-Preferential DFR-Like Gene Encoding Dihydrokaempferol Reductase Involved in Anthocyanin Biosynthesis of Purple-Fleshed Sweet Potato

机译:紫色二化甘薯花青素生物合成的根优先DFR样基因编码二氢山ka酚还原酶。

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摘要

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 (IbDHKR) 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 IbDHKR was expressed in all the tested organs, but with much higher level in tuber roots. The expression level of IbDHKR 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, IbDHKR 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.
机译:由于块茎中含有丰富的花青素,紫皮甘薯对健康有益。尽管花青素的生物合成途径已在植物的地上器官中得到很好的理解,但地下块茎中花青素的生物合成知识仍然有限。在本研究中,我们从紫色肉甘薯中分离了一个编码二氢山hydro酚还原酶(IbDHKR)的根优先基因并对其功能进行了表征。在序列水平上,IbDHKR与其他植物中报道的二氢黄酮醇还原酶高度相似,在IbDHKR中也发现了NADPH结合基序和底物结合域。组织概况显示,IbDHKR在所有测试器官中均有表达,但在块根中的表达水平更高。 IbDHKR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。纯化了重组的44 kD IbDHKR,并通过三种不同的二氢黄酮醇底物(包括二氢山my酚(DHK),二氢槲皮素和二氢myrecetin)进料。底物进料分析表明,IbDHKR仅接受DHK作为底物,LC-MS证实该底物被还原为亮白油精。最后,IbDHKR在转基因烟草中过表达。与野生型花冠相比,IbDHKR过表达的烟草花冠色素较高,花色苷含量更高。总而言之,IbDHKR是参与花色苷生物合成的根源优先基因,其编码蛋白(特别是催化DHK还原以生成白椰油精蛋白)是工程化花色苷生物合成途径的候选基因。

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