Production of Kinanthraquinone D with Antimalarial Activity by Heterologous Gene Expression and Biotransformation in Streptomyces lividans TK23

被引:0
|
作者
Sakai, Katsuyuki [1 ]
Futamura, Yushi [2 ]
Nogawa, Toshihiko [3 ]
Zhao, Yuzhu [1 ,4 ]
Koshino, Hiroyuki [3 ]
Osada, Hiroyuki [2 ]
Takahashi, Shunji [1 ,4 ]
机构
[1] RIKEN Ctr Sustainable Resource Sci, Nat Prod Biosynth Res Unit, Wako, Saitama 3510198, Japan
[2] REKEN Ctr Sustainable Resource Sci, Chem Resource Dev Unit, Wako, Saitama 3510198, Japan
[3] RIKEN Ctr Sustainable Resource Sci, Technol Platform Div, Mol Struct Characterizat Unit, Wako, Saitama 3510198, Japan
[4] Saitama Univ, Grad Sch Sci & Engn, Saitama, Saitama 3388570, Japan
来源
JOURNAL OF NATURAL PRODUCTS | 2024年 / 87卷 / 04期
基金
日本学术振兴会;
关键词
IDENTIFICATION; CLUSTER;
D O I
10.1021/acs.jnatprod.3c01076
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
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 mu M, respectively, without cytotoxicity up to 30 mu M.
引用
收藏
页码:855 / 860
页数:6
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