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A Genome-Centric Approach Reveals a Novel Glycosyltransferase from the GA A07 Strain of Bacillus thuringiensis Responsible for Catalyzing 15-O-Glycosylation of Ganoderic Acid A.
Chang, Te-Sheng; Wang, Tzi-Yuan; Hsueh, Tzu-Yu; Lee, Yu-Wen; Chuang, Hsin-Mei; Cai, Wen-Xuan; Wu, Jiumn-Yih; Chiang, Chien-Min; Wu, Yu-Wei.
  • Chang TS; Department of Biological Sciences and Technology, National University of Tainan, Tainan 70005, Taiwan. mozyme2001@gmail.com.
  • Wang TY; Biodiversity Research Center, Academia Sinica, Taipei 11529, Taiwan. tziyuan@gmail.com.
  • Hsueh TY; Department of Biological Sciences and Technology, National University of Tainan, Tainan 70005, Taiwan. vuvu99983@gmail.com.
  • Lee YW; Department of Biological Sciences and Technology, National University of Tainan, Tainan 70005, Taiwan. s10458017@gm2.nutn.edu.tw.
  • Chuang HM; Department of Biological Sciences and Technology, National University of Tainan, Tainan 70005, Taiwan. tiffany170420@gmail.com.
  • Cai WX; Department of Biological Sciences and Technology, National University of Tainan, Tainan 70005, Taiwan. amy19990630@yahoo.com.tw.
  • Wu JY; Department of Food Science, National Quemoy University, Kinmen County 892, Taiwan. wujy@nqu.edu.tw.
  • Chiang CM; Department of Biotechnology, Chia Nan University of Pharmacy and Science, No. 60, Erh-Jen Rd., Sec. 1, Jen-Te District, Tainan 71710, Taiwan. cmchiang@mail.cnu.edu.tw.
  • Wu YW; Graduate Institute of Biomedical Informatics, College of Medical Science and Technology, Taipei Medical University, Taipei 11031, Taiwan. yuwei.wu@tmu.edu.tw.
Int J Mol Sci ; 20(20)2019 Oct 20.
Article en En | MEDLINE | ID: mdl-31635144
Strain GA A07 was identified as an intestinal Bacillus bacterium of zebrafish, which has high efficiency to biotransform the triterpenoid, ganoderic acid A (GAA), into GAA-15-O-ß-glucoside. To date, only two known enzymes (BsUGT398 and BsUGT489) of Bacillus subtilis ATCC 6633 strain can biotransform GAA. It is thus worthwhile to identify the responsible genes of strain GA A07 by whole genome sequencing. A complete genome of strain GA A07 was successfully assembled. A phylogenomic analysis revealed the species of the GA A07 strain to be Bacillus thuringiensis. Forty glycosyltransferase (GT) family genes were identified from the complete genome, among which three genes (FQZ25_16345, FQZ25_19840, and FQZ25_19010) were closely related to BsUGT398 and BsUGT489. Two of the three candidate genes, FQZ25_16345 and FQZ25_19010, were successfully cloned and expressed in a soluble form in Escherichia coli, and the corresponding proteins, BtGT_16345 and BtGT_19010, were purified for a biotransformation activity assay. An ultra-performance liquid chromatographic analysis further confirmed that only the purified BtGT_16345 had the key biotransformation activity of catalyzing GAA into GAA-15-O-ß-glucoside. The suitable conditions for this enzyme activity were pH 7.5, 10 mM of magnesium ions, and 30 °C. In addition, BtGT_16345 showed glycosylation activity toward seven flavonoids (apigenein, quercetein, naringenein, resveratrol, genistein, daidzein, and 8-hydroxydaidzein) and two triterpenoids (GAA and antcin K). A kinetic study showed that the catalytic efficiency (kcat/KM) of BtGT_16345 was not significantly different compared with either BsUGT398 or BsUGT489. In short, this study identified BtGT_16345 from B. thuringiensis GA A07 is the catalytic enzyme responsible for the 15-O-glycosylation of GAA and it was also regioselective toward triterpenoid substrates.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Bacillus thuringiensis / Proteínas Bacterianas / Glicosiltransferasas / Genoma Bacteriano / Ácidos Heptanoicos / Lanosterol Idioma: En Año: 2019 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Bacillus thuringiensis / Proteínas Bacterianas / Glicosiltransferasas / Genoma Bacteriano / Ácidos Heptanoicos / Lanosterol Idioma: En Año: 2019 Tipo del documento: Article