Lewis Jacob A, Zhang Bixia, Harza Rishi, Palmer Nathan, Sarath Gautam, Sattler Scott E, Twigg Paul, Vermerris Wilfred, Kang ChulHee
Department of Chemistry, Washington State University, Pullman, WA 99164, USA.
Wheat, Sorghum, Forage Research Unit, U.S. Department of Agriculture-Agricultural Research Service, Lincoln, NE 68583, USA.
Int J Mol Sci. 2023 Sep 9;24(18):13901. doi: 10.3390/ijms241813901.
Flavonoids are potent antioxidants that play a role in defense against pathogens, UV-radiation, and the detoxification of reactive oxygen species. Dihydroflavonol 4-reductase (DFR) and flavanone 4-reductase (FNR) reduce dihydroflavonols and flavanones, respectively, using NAD(P)H to produce flavan-(3)-4-(di)ols in flavonoid biosynthesis. Anthocyanidin reductase (ANR) reduces anthocyanidins to flavan-3-ols. In addition to their sequences, the 3D structures of recombinant DFR, FNR and ANR from sorghum and switchgrass showed a high level of similarity. The catalytic mechanism, substrate-specificity and key residues of three reductases were deduced from crystal structures, site-directed mutagenesis, molecular docking, kinetics, and thermodynamic ana-lyses. Although DFR displayed its highest activity against dihydroflavonols, it also showed activity against flavanones and anthocyanidins. It was inhibited by the flavonol quercetin and high concentrations of dihydroflavonols/flavonones. SbFNR1 and SbFNR2 did not show any activity against dihydroflavonols. However, SbFNR1 displayed activity against flavanones and ANR activity against two anthocyanidins, cyanidin and pelargonidin. Therefore, SbFNR1 and SbFNR2 could be specific ANR isozymes without delphinidin activity. Sorghum has high concentrations of 3-deoxyanthocyanidins in vivo, supporting the observed high activity of SbDFR against flavonols. Mining of expression data indicated substantial induction of these three reductase genes in both switchgrass and sorghum in response to biotic stress. Key signature sequences for proper DFR/ANR classification are proposed and could form the basis for future metabolic engineering of flavonoid metabolism.
黄酮类化合物是强效抗氧化剂,在抵御病原体、紫外线辐射以及活性氧解毒过程中发挥作用。二氢黄酮醇4-还原酶(DFR)和黄烷酮4-还原酶(FNR)分别利用NAD(P)H还原二氢黄酮醇和黄烷酮,在类黄酮生物合成中生成黄烷-(3)-4-(二)醇。花青素还原酶(ANR)将花青素还原为黄烷-3-醇。除了序列之外,来自高粱和柳枝稷的重组DFR、FNR和ANR的三维结构显示出高度相似性。通过晶体结构、定点诱变、分子对接、动力学和热力学分析推导了三种还原酶的催化机制、底物特异性和关键残基。虽然DFR对二氢黄酮醇表现出最高活性,但它对黄烷酮和花青素也有活性。它受到黄酮醇槲皮素以及高浓度二氢黄酮醇/黄烷酮的抑制。SbFNR1和SbFNR2对二氢黄酮醇没有任何活性。然而,SbFNR1对黄烷酮有活性,对两种花青素矢车菊素和天竺葵素具有ANR活性。因此,SbFNR1和SbFNR2可能是没有翠雀素活性的特异性ANR同工酶。高粱体内含有高浓度的3-脱氧花青素,这支持了观察到的SbDFR对黄酮醇的高活性。表达数据挖掘表明,柳枝稷和高粱中的这三个还原酶基因在受到生物胁迫时均有大量诱导表达。提出了用于正确DFR/ANR分类的关键特征序列,可为未来类黄酮代谢的代谢工程奠定基础。