Faculty of Biology, Genetics and Genomics of Plants, Bielefeld University, 33615, Bielefeld, Germany.
Research and Innovation Centre, Fondazione Edmund Mach, 38098, San Michele all'Adige (TN), Italy.
BMC Plant Biol. 2024 Feb 9;24(1):99. doi: 10.1186/s12870-024-04787-1.
Flavonoids are plant specialised metabolites, which derive from phenylalanine and acetate metabolism. They possess a variety of beneficial characteristics for plants and humans. Several modification steps in the synthesis of tricyclic flavonoids cause for the amazing diversity of flavonoids in plants. The 2-oxoglutarate-dependent dioxygenases (2-ODDs) flavanone 3-hydroxylase (F3H, synonym FHT), flavonol synthase (FLS) and anthocyanidin synthase (ANS, synonym leucoanthocyanidin dioxygenase (LDOX)), catalyse oxidative modifications to the central C ring. They are highly similar and have been shown to catalyse, at least in part, each other's reactions. FLS and ANS have been identified as bifunctional enzymes in many species, including Arabidopsis thaliana, stressing the capability of plants to bypass missing or mutated reaction steps on the way to flavonoid production. However, little is known about such bypass reactions and the flavonoid composition of plants lacking all three central flavonoid 2-ODDs.
To address this issue, we generated a f3h/fls1/ans mutant, as well as the corresponding double mutants and investigated the flavonoid composition of this mutant collection. The f3h/fls1/ans mutant was further characterised at the genomic level by analysis of a nanopore DNA sequencing generated genome sequence assembly and at the transcriptomic level by RNA-Seq analysis. The mutant collection established, including the novel double mutants f3h/fls1 and f3h/ans, was used to validate and analyse the multifunctionalities of F3H, FLS1, and ANS in planta. Metabolite analyses revealed the accumulation of eriodictyol and additional glycosylated derivatives in mutants carrying the f3h mutant allele, resulting from the conversion of naringenin to eriodictyol by flavonoid 3'-hydroxylase (F3'H) activity.
We describe the in planta multifunctionality of the three central flavonoid 2-ODDs from A. thaliana and identify a bypass in the f3h/fls1/ans triple mutant that leads to the formation of eriodictyol derivatives. As (homo-)eriodictyols are known as bitter taste maskers, the annotated eriodictyol (derivatives) and in particular the observations made on their in planta production, could provide valuable insights for the creation of novel food supplements.
类黄酮是植物特有的代谢物,来源于苯丙氨酸和乙酸代谢。它们对植物和人类具有多种有益特性。在三环类黄酮的合成中有几个修饰步骤导致了植物中类黄酮的惊人多样性。2-氧戊二酸依赖性双加氧酶(2-ODD)类黄酮 3-羟化酶(F3H,同义词 FHT)、类黄酮合酶(FLS)和花青素合酶(ANS,同义词无色花青素双加氧酶(LDOX)),催化中央 C 环的氧化修饰。它们非常相似,并已被证明至少部分催化彼此的反应。FLS 和 ANS 在许多物种中已被鉴定为双功能酶,包括拟南芥,这强调了植物在黄酮类化合物生产过程中绕过缺失或突变反应步骤的能力。然而,对于这种旁路反应以及缺乏所有三种中心类黄酮 2-ODD 的植物的类黄酮组成知之甚少。
为了解决这个问题,我们生成了 f3h/fls1/ans 突变体,以及相应的双突变体,并研究了该突变体集合的类黄酮组成。通过分析纳米孔 DNA 测序生成的基因组序列组装,在基因组水平上进一步表征了 f3h/fls1/ans 突变体,并通过 RNA-Seq 分析在转录组水平上进行了表征。建立的突变体集合,包括新型双突变体 f3h/fls1 和 f3h/ans,用于验证和分析 F3H、FLS1 和 ANS 在植物体内的多功能性。代谢产物分析表明,在携带 f3h 突变等位基因的突变体中积累了圣草酚和其他糖基化衍生物,这是由于类黄酮 3'-羟化酶(F3'H)活性将柚皮素转化为圣草酚所致。
我们描述了来自拟南芥的三种中心类黄酮 2-ODD 的体内多功能性,并鉴定了 f3h/fls1/ans 三重突变体中的一个旁路,该旁路导致圣草酚衍生物的形成。由于(同)圣草酚被认为是苦味掩蔽剂,因此注释的圣草酚(衍生物),特别是在其体内产生方面的观察结果,可能为新型食品补充剂的创造提供有价值的见解。