《Table S3 1H and 13C NMR data of anthrachamycin in DMSO-d6(600 MHz)》
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《恰塔努加链霉菌L10中rpoB基因突变激活蒽塔恰霉素生物合成基因簇的研究(英文)》
The bacterial strains used in this study are listed in Table S1.S.chattanoogensis L10 and its derivatives were grown at 28°C on yeast extract-malt extractglucose(YMG)solid medium.Trypticase soy broth was used for extracting genomic DNA(Du et al.,2011).Escherichia coli DH5αand E.coli BL21(DE3)were used as cloning and expression hosts,respectively.E.coli cells were cultured in Luria-Bertani broth(LB)medium with the appropriate concentration of antibiotics for propagating plasmids.
图表编号 | XD00113737600 严禁用于非法目的 |
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绘制时间 | 2019.12.03 |
作者 | Zi-yue LI、Qing-ting BU、Jue WANG、Yu LIU、Xin-ai CHEN、Xu-ming MAO、Yong-Quan LI |
绘制单位 | Institute of Pharmaceutical Biotechnology & First Affiliated Hospital, School of Medicine, Zhejiang University、Zhejiang Provincial Key Laboratory for Microbial Biochemistry and Metabolic Engineering、Institute of Pharmaceutical Biotechnology & First Affili |
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