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催化柑橘类植物中二 - C - 葡萄糖基黄酮形成的C - 糖基转移酶。

C-Glycosyltransferases catalyzing the formation of di-C-glucosyl flavonoids in citrus plants.

作者信息

Ito Takamitsu, Fujimoto Shunsuke, Suito Fumiaki, Shimosaka Makoto, Taguchi Goro

机构信息

Department of Applied Biology, Faculty of Textile Science and Technology, Shinshu University, 3-15-1 Tokida, Ueda, 386-8567, Japan.

出版信息

Plant J. 2017 Jul;91(2):187-198. doi: 10.1111/tpj.13555. Epub 2017 Jun 5.

Abstract

Citrus plants accumulate many kinds of flavonoids, including di-C-glucosyl flavonoids, which have attracted considerable attention due to their health benefits. However, the biosynthesis of di-C-glucosyl flavonoids has not been elucidated at the molecular level. Here, we identified the C-glycosyltransferases (CGTs) FcCGT (UGT708G1) and CuCGT (UGT708G2) as the primary enzymes involved in the biosynthesis of di-C-glucosyl flavonoids in the citrus plants kumquat (Fortunella crassifolia) and satsuma mandarin (Citrus unshiu), respectively. The amino acid sequences of these CGTs were 98% identical, indicating that CGT genes are highly conserved in the citrus family. The recombinant enzymes FcCGT and CuCGT utilized 2-hydroxyflavanones, dihydrochalcone, and their mono-C-glucosides as sugar acceptors and produced corresponding di-C-glucosides. The K and k values of FcCGT toward phloretin were <0.5 μm and 12.0 sec , and those toward nothofagin (3'-C-glucosylphloretin) were 14.4 μm and 5.3 sec , respectively; these values are comparable with those of other glycosyltransferases reported to date. Transcripts of both CGT genes were found to concentrate in various plant organs, and particularly in leaves. Our results suggest that di-C-glucosyl flavonoid biosynthesis proceeds via a single enzyme using either 2-hydroxyflavanones or phloretin as a substrate in citrus plants. In addition, Escherichia coli cells expressing CGT genes were found to be capable of producing di-C-glucosyl flavonoids, which is promising for commercial production of these valuable compounds.

摘要

柑橘类植物会积累多种黄酮类化合物,包括二 - C - 葡萄糖基黄酮类化合物,由于它们对健康有益,因此受到了广泛关注。然而,二 - C - 葡萄糖基黄酮类化合物的生物合成在分子水平上尚未阐明。在此,我们分别鉴定出金橘(Fortunella crassifolia)和温州蜜柑(Citrus unshiu)中参与二 - C - 葡萄糖基黄酮类化合物生物合成的主要酶,即C - 糖基转移酶(CGT)FcCGT(UGT708G1)和CuCGT(UGT708G2)。这些CGT的氨基酸序列有98%的同一性,这表明CGT基因在柑橘家族中高度保守。重组酶FcCGT和CuCGT利用2 - 羟基黄烷酮、二氢查耳酮及其单 - C - 葡萄糖苷作为糖受体,并产生相应的二 - C - 葡萄糖苷。FcCGT对根皮素的K值和k值分别<0.5μm和12.0秒,对诺托法金(3'-C - 葡萄糖基根皮素)的K值和k值分别为14.4μm和5.3秒;这些值与迄今报道的其他糖基转移酶的值相当。发现这两个CGT基因的转录本集中在各种植物器官中,尤其是在叶片中。我们的结果表明,在柑橘类植物中,二 - C - 葡萄糖基黄酮类化合物的生物合成通过一种单一的酶进行,该酶以2 - 羟基黄烷酮或根皮素为底物。此外,发现表达CGT基因的大肠杆菌细胞能够产生二 - C - 葡萄糖基黄酮类化合物,这对于这些有价值化合物的商业生产很有前景。

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