{"title":"传统药用植物紫花土巴葛生产褐黄蛋白的区域特异性s加氧酶的鉴定。","authors":"Jichen Wang, Hideyuki Suzuki, Nanako Nakashima, Mariko Kitajima, Hiromitsu Takayama, Kazuki Saito, Mami Yamazaki, Naoko Yoshimoto","doi":"10.5511/plantbiotechnology.22.0619a","DOIUrl":null,"url":null,"abstract":"<p><p>Marasmin [<i>S</i>-(methylthiomethyl)-L-cysteine-4-oxide] is a pharmaceutically valuable sulfur-containing compound produced by the traditional medicinal plant, <i>Tulbaghia violacea</i>. Here, we report the identification of an <i>S</i>-oxygenase, TvMAS1, that produces marasmin from its corresponding sulfide, <i>S</i>-(methylthiomethyl)-L-cysteine. The amino acid sequence of TvMAS1 showed high sequence similarity to known flavin-containing <i>S</i>-oxygenating monooxygenases in plants. Recombinant TvMAS1 catalyzed regiospecific <i>S</i>-oxygenation at S4 of <i>S</i>-(methylthiomethyl)-L-cysteine to yield marasmin, with an apparent <i>K</i> <sub>m</sub> value of 0.55 mM. <i>TvMAS1</i> mRNA accumulated with <i>S</i>-(methylthiomethyl)-L-cysteine and marasmin in various organs of <i>T. violacea</i>. Our findings suggest that TvMAS1 catalyzes the <i>S</i>-oxygenation reaction during the last step of marasmin biosynthesis in <i>T. violacea</i>.</p>","PeriodicalId":520754,"journal":{"name":"Plant biotechnology (Tokyo, Japan)","volume":" ","pages":"281-289"},"PeriodicalIF":1.1000,"publicationDate":"2022-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9592931/pdf/plantbiotechnology-39-3-22.0619a.pdf","citationCount":"0","resultStr":"{\"title\":\"Identification of a regiospecific <i>S</i>-oxygenase for the production of marasmin in traditional medicinal plant <i>Tulbaghia violacea</i>.\",\"authors\":\"Jichen Wang, Hideyuki Suzuki, Nanako Nakashima, Mariko Kitajima, Hiromitsu Takayama, Kazuki Saito, Mami Yamazaki, Naoko Yoshimoto\",\"doi\":\"10.5511/plantbiotechnology.22.0619a\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Marasmin [<i>S</i>-(methylthiomethyl)-L-cysteine-4-oxide] is a pharmaceutically valuable sulfur-containing compound produced by the traditional medicinal plant, <i>Tulbaghia violacea</i>. Here, we report the identification of an <i>S</i>-oxygenase, TvMAS1, that produces marasmin from its corresponding sulfide, <i>S</i>-(methylthiomethyl)-L-cysteine. The amino acid sequence of TvMAS1 showed high sequence similarity to known flavin-containing <i>S</i>-oxygenating monooxygenases in plants. Recombinant TvMAS1 catalyzed regiospecific <i>S</i>-oxygenation at S4 of <i>S</i>-(methylthiomethyl)-L-cysteine to yield marasmin, with an apparent <i>K</i> <sub>m</sub> value of 0.55 mM. <i>TvMAS1</i> mRNA accumulated with <i>S</i>-(methylthiomethyl)-L-cysteine and marasmin in various organs of <i>T. violacea</i>. Our findings suggest that TvMAS1 catalyzes the <i>S</i>-oxygenation reaction during the last step of marasmin biosynthesis in <i>T. violacea</i>.</p>\",\"PeriodicalId\":520754,\"journal\":{\"name\":\"Plant biotechnology (Tokyo, Japan)\",\"volume\":\" \",\"pages\":\"281-289\"},\"PeriodicalIF\":1.1000,\"publicationDate\":\"2022-09-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9592931/pdf/plantbiotechnology-39-3-22.0619a.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant biotechnology (Tokyo, Japan)\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://doi.org/10.5511/plantbiotechnology.22.0619a\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant biotechnology (Tokyo, Japan)","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.5511/plantbiotechnology.22.0619a","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
黄芪黄酮[S-(甲基硫甲基)- l -半胱氨酸-4-氧化物]是一种具有药用价值的含硫化合物,由传统药用植物紫花郁金香(Tulbaghia violacea)生产。在这里,我们报道了一种S-加氧酶TvMAS1的鉴定,它可以从相应的硫化物S-(甲基硫甲基)- l -半胱氨酸中产生褐黄蛋白。TvMAS1的氨基酸序列与植物中已知的含黄素s -氧合单加氧酶具有较高的序列相似性。重组TvMAS1在S-(甲基硫甲基)- l -半胱氨酸的S4位点催化区域特异性S-氧合,得到红素,表观K m值为0.55 mM。TvMAS1 mRNA随S-(甲基硫甲基)- l -半胱氨酸和黄颡鱼蛋白在堇菜各器官中积累。我们的研究结果表明,TvMAS1在紫花草中催化了紫花草蛋白合成的最后一步s -氧合反应。
Identification of a regiospecific S-oxygenase for the production of marasmin in traditional medicinal plant Tulbaghia violacea.
Marasmin [S-(methylthiomethyl)-L-cysteine-4-oxide] is a pharmaceutically valuable sulfur-containing compound produced by the traditional medicinal plant, Tulbaghia violacea. Here, we report the identification of an S-oxygenase, TvMAS1, that produces marasmin from its corresponding sulfide, S-(methylthiomethyl)-L-cysteine. The amino acid sequence of TvMAS1 showed high sequence similarity to known flavin-containing S-oxygenating monooxygenases in plants. Recombinant TvMAS1 catalyzed regiospecific S-oxygenation at S4 of S-(methylthiomethyl)-L-cysteine to yield marasmin, with an apparent Km value of 0.55 mM. TvMAS1 mRNA accumulated with S-(methylthiomethyl)-L-cysteine and marasmin in various organs of T. violacea. Our findings suggest that TvMAS1 catalyzes the S-oxygenation reaction during the last step of marasmin biosynthesis in T. violacea.