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Production of Kinanthraquinone D with Antimalarial Activity by Heterologous Gene Expression and Biotransformation in Streptomyces lividans TK23.
Sakai, Katsuyuki; Futamura, Yushi; Nogawa, Toshihiko; Zhao, Yuzhu; Koshino, Hiroyuki; Osada, Hiroyuki; Takahashi, Shunji.
Afiliação
  • Sakai K; Natural Product Biosynthesis Research Unit, RIKEN Center for Sustainable Resource Science, 2-1 Hirosawa, Wako, Saitama 351-0198, Japan.
  • Futamura Y; Chemical Resource Development Unit, REKEN Center for Sustainable Resource Science, 2-1 Hirosawa, Wako, Saitama 351-0198, Japan.
  • Nogawa T; Molecular Structure Characterization Unit, Technology Platform Division, REKEN Center for Sustainable Resource Science, 2-1 Hirosawa, Wako, Saitama 351-0198, Japan.
  • Zhao Y; Natural Product Biosynthesis Research Unit, RIKEN Center for Sustainable Resource Science, 2-1 Hirosawa, Wako, Saitama 351-0198, Japan.
  • Koshino H; Graduate School of Science and Engineering, Saitama University; Shimo-Okubo 255, Sakura-ku, Saitama-shi, Saitama 338-8570, Japan.
  • Osada H; Molecular Structure Characterization Unit, Technology Platform Division, REKEN Center for Sustainable Resource Science, 2-1 Hirosawa, Wako, Saitama 351-0198, Japan.
  • Takahashi S; Chemical Resource Development Unit, REKEN Center for Sustainable Resource Science, 2-1 Hirosawa, Wako, Saitama 351-0198, Japan.
J Nat Prod ; 87(4): 855-860, 2024 Apr 26.
Article em En | MEDLINE | ID: mdl-38412225
ABSTRACT
Two new compounds, kinanthraquinone C (1) and kinanthraquinone D (2), were isolated along with two known compounds, kinanthraquinone (3) and kinanthraquinone B (4), produced by the heterologous expression of the kiq biosynthetic gene cluster and its pathway-specific regulator, kiqA, in Streptomyces lividans TK23. The chemical structures of compounds 1 and 2 were determined using mass spectrometry and nuclear magnetic resonance analyses. To examine a biosynthetic pathway of compounds 1 and 2, incubation experiments were conducted using S. lividans TK23 to supply the compounds 3 and 4. These experiments indicated that compounds 3 and 4 were converted to compounds 2 and 1, respectively, by the endogenous enzymes of S. lividans TK23. Compounds 2, 3, and 4 had antimalarial activities at half-maximal inhibitory concentration values of 0.91, 1.2, and 15 µM, respectively, without cytotoxicity up to 30 µM.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antraquinonas / Streptomyces lividans / Antimaláricos Idioma: En Revista: J Nat Prod Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antraquinonas / Streptomyces lividans / Antimaláricos Idioma: En Revista: J Nat Prod Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Japão