Department of Research and Development, Kazusa DNA Research Institute, 2-6-7 Kazusa-Kamatari, Kisarazu, Chiba, 292-0818 Japan.
Research and Development Department, Hirata Corporation, 111 Hitotsugi, Ueki, Kita, Kumamoto-shi, Kumamoto, 861-0198 Japan.
Plant Cell Physiol. 2021 Jul 17;62(3):411-423. doi: 10.1093/pcp/pcaa171.
Lotus japonicus is a model legume that accumulates 8-hydroxyflavonol derivatives, such as gossypetin (8-hydroxyquercetin) 3-O-glycoside, which confer the yellow color to its petals. An enzyme, flavonoid 8-hydroxylase (F8H; LjF8H), is assumed to be involved in the biosynthesis, but the specific gene is yet to be identified. The LjF8H cDNA was isolated as a flavin adenine dinucleotide (FAD)-binding monooxygenase-like protein using flower buds and flower-specific EST data of L. japonicus. LjF8H is a single copy gene on chromosome III consisting of six exons. The conserved FAD- and NAD(P)H-dependent oxidase motifs were found in LjF8H. Phylogenetic analysis suggested that LjF8H is a member of the flavin monooxygenase group but distinctly different from other known flavonoid oxygenases. Analysis of recombinant yeast microsome expressing LjF8H revealed that the enzyme catalyzed the 8-hydroxylation of quercetin. Other flavonoids, such as naringenin, eriodictyol, apigenin, luteolin, taxifolin and kaempferol, also acted as substrates of LjF8H. This broad substrate acceptance was unlike known F8Hs in other plants. Interestingly, flavanone and flavanonol, which have saturated C-C bond at positions 2 and 3 of the flavonoid C-ring, produced 6-hyroxylflavonoids as a by-product of the enzymatic reaction. Furthermore, LjF8H only accepted the 2S-isomer of naringenin, suggesting that the conformational state of the substrates might affect product specificity. The overexpression of LjF8H in Arabidopsis thaliana and Petunia hybrida synthesized gossypetin and 8-hydroxykaempferol, respectively, indicating that LjF8H was functional in plant cells. In conclusion, this study represents the first instance of cloning and identification of F8Hs responsible for gossypetin biosynthesis.
百脉根是一种模式豆科植物,积累 8-羟基黄酮醇衍生物,如花萼豆素(8-羟基槲皮素)3-O-糖苷,使花瓣呈现黄色。一种酶,类黄素单加氧酶(F8H;LjF8H),被认为参与生物合成,但特定的基因尚未被确定。使用百脉根花蕾和花特异性 EST 数据,从 cDNA 文库中分离出 LjF8H 的 cDNA,它是一种黄素腺嘌呤二核苷酸(FAD)结合单加氧酶样蛋白。LjF8H 是位于染色体 III 上的单拷贝基因,由六个外显子组成。在 LjF8H 中发现了保守的 FAD 和 NAD(P)H 依赖性氧化酶基序。系统发育分析表明,LjF8H 是黄素单加氧酶组的成员,但与其他已知的黄酮氧合酶明显不同。表达 LjF8H 的重组酵母微粒体分析表明,该酶催化槲皮素的 8-羟化。其他类黄酮,如柚皮素、圣草酚、芹菜素、木犀草素、杨梅素和山奈酚,也可作为 LjF8H 的底物。这种广泛的底物接受与其他植物中的已知 F8H 不同。有趣的是,在黄酮酮和黄烷酮中,黄酮 C 环 2 和 3 位的 C-C 键饱和,作为酶促反应的副产物产生 6-羟黄酮。此外,LjF8H 仅接受柚皮素的 2S-异构体,表明底物的构象状态可能影响产物特异性。LjF8H 在拟南芥和矮牵牛中的过表达分别合成了棉子糖和 8-羟基山奈酚,表明 LjF8H 在植物细胞中具有功能。总之,这项研究代表了克隆和鉴定负责棉子糖生物合成的 F8H 的首例。