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金针菇(伞菌纲)中麦角硫因的生物合成途径

The Biosynthetic Pathway of Ergothioneine in Culinary-Medicinal Winter Mushroom, Flammulina velutipes (Agaricomycetes).

作者信息

Yang Xueqin, Lin Shuoxin, Lin Jinde, Wang Yuyao, Lin Jun-Fang, Guo Liqiong

机构信息

Department of Bioengineering, College of Food Science & Institute of Food Biotechnology, South China Agricultural University, Guangzhou 510640, China; Research Center for Micro-Ecological Agent Engineering and Technology of Guangdong Province, Guangzhou 510640, China.

James Clark School of Engineering, University of Maryland, College Park, MD 20742, USA.

出版信息

Int J Med Mushrooms. 2020;22(2):171-181. doi: 10.1615/IntJMedMushrooms.2020033826.

Abstract

Ergothioneine is a natural 2-thiol-amidazole amino acid that plays an important role in inflammation, depression, and cardiovascular disease. Flammulina velutipes is a common basidiomycete mushroom rich in ergothioneine (EGT). However, the biosynthetic pathway of EGT in F. velutipes is still unclear. In this study, the F. velutipes ergothioneine biosynthetic gene 1 (Fvegtl), F. velutipes ergothioneine biosynthetic gene 2 (Fvegt2), and F. velutipes ergothioneine biosynthetic gene 3 (Fvegt3) were cloned and expressed, and the activities of the proteins encoded by these three genes (FvEgt1, F. velutipes ergothioneine biosynthase 1; FvEgt2, F. velutipes ergothioneine biosynthase 2; and FvEgt3, F. velutipes ergothioneine biosynthase 3) were identified. The results showed that FvEgtl not only has the function of methyltransferase, but also has the function of hercynlcysteineteine sulfoxide (Hersul) synthase, which can catalyze the production of Hersul from histidine and cysteine in F. velutipes. FvEgt2 and FvEgt3 are two functionally different cysteine desulfurase enzymes. Among them, FvEgt2 is a cysteine-cysteine desulfurase-which catalyzes the activation of the S-H bond on cysteine, while FvEgt3 is a pyridoxal phosphate (PLP)-dependent cysteine desulfurase responsible for catalyzing the production of ketimine complex. Our results show that FvEgt1/FvEgt2/FvEgt3 can simultaneously catalyze the production of EGT by histidine, cysteine, and pyridoxal phosphate. Collectively, the in vitro synthesis of EGT in the edible fungus F. velutipes was first achieved, which laid the foundation for the biological production of EGT.

摘要

麦角硫因是一种天然的2-硫醇基咪唑氨基酸,在炎症、抑郁症和心血管疾病中发挥着重要作用。金针菇是一种常见的富含麦角硫因(EGT)的担子菌。然而,金针菇中EGT的生物合成途径仍不清楚。在本研究中,克隆并表达了金针菇麦角硫因生物合成基因1(Fvegt1)、金针菇麦角硫因生物合成基因2(Fvegt2)和金针菇麦角硫因生物合成基因3(Fvegt3),并鉴定了这三个基因编码的蛋白质(FvEgt1,金针菇麦角硫因合酶1;FvEgt2,金针菇麦角硫因合酶2;FvEgt3,金针菇麦角硫因合酶3)的活性。结果表明,FvEgt1不仅具有甲基转移酶的功能,还具有组氨酸半胱氨酸亚砜(Hersul)合酶的功能,它可以催化金针菇中组氨酸和半胱氨酸生成Hersul。FvEgt2和FvEgt3是两种功能不同的半胱氨酸脱硫酶。其中,FvEgt2是一种半胱氨酸-半胱氨酸脱硫酶,催化半胱氨酸上S-H键的活化,而FvEgt3是一种依赖磷酸吡哆醛(PLP)的半胱氨酸脱硫酶,负责催化生成酮亚胺复合物。我们的结果表明,FvEgt1/FvEgt2/FvEgt3可以同时催化由组氨酸、半胱氨酸和磷酸吡哆醛生成EGT。总的来说,首次实现了食用菌金针菇中EGT的体外合成,为EGT的生物生产奠定了基础。

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