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Tissue-specific and intracellular localization of indican synthase from Polygonum tinctorium

机译:来自胶凝胶质蛋白的籼型合成酶的组织特异性和细胞内定位

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摘要

The plant Polygonum tinctorium produces the secondary metabolite indican (indoxyl-beta-D-glucoside), a precursor of the blue dye indigo. P. tinctorium synthesizes indican through the actions of the UDP-glucosyltransferase (UGT), indican synthase. Herein, we partially purified an indican synthase from the leaves and subsequently performed peptide mass fingerprinting analysis. Consequently, we identified a fragment that was homologous to a UDP-glucosyltransferase 72B (UGT72B) family member. We named it PtIgs (P. tinctorium indoxyl-beta-D-glucoside synthase) and obtained the full-length cDNA using rapid amplification of the cDNA ends. The primary structure of PtIGS, which Ptlgs encoded, showed high identity with indican synthases (ItUGT1 and ItUGT2) from Indigofera tinctoria (Inoue et al., 2017). Moreover, in expression analyses of P. tinctorium, PtIGS mRNA was virtually found only in the leaves, was most highly expressed in the 1st leaves, and decreased with leaf age. Because PtIGS expression tended to reflect indican contents and synthesis activities, we concluded that PtIGS functions as an indican synthase in plant cells.
机译:植物聚宝脂酊剂产生次级代谢物籼(吲哚基-D-葡糖苷),是蓝染料靛蓝的前体。 P.酊剂通过UDP-葡糖基转移酶(UGT),indiaman合酶的作用合成indipan。这里,我们部分纯化叶片的籼型合成酶,随后进行肽质量指纹分析。因此,我们鉴定了对UDP-葡糖基转移酶72B(UGT72B)家族构件同源的片段。我们将其命名为ptigs(P.Tinctorium吲哚基-D-葡糖苷合酶),并使用CDNA的快速扩增获得全长cDNA。 PTIG的主要结构,PTLG编码,从Indigofera Tanctoria(Inoue等,2017)的indane合成酶(Itugt1和Itugt2)显示出高度的身份。此外,在P.Tinctium的表达分析中,Ptigs mRNA实际上仅在叶片中发现,在第1叶中最高度表达,并且随着叶龄而降低。因为ptigs表达倾向于反映incoran含量和合成活性,所以我们得出结论,Ptigs用作植物细胞中的籼型合酶。

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