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Comment on “A commensal strain of Staphylococcus epidermidis protects against skin neoplasia” by Nakatsuji et al.

机译:Nakatsuji等人评论“表皮葡萄球菌共生菌株可预防皮肤肿瘤”。

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A recent article in Science Advances described the striking discovery that the commensal Staphylococcus epidermidis strain MO34 displays antimicrobial and antitumor activities by producing a small molecule, identified as the nucleobase analog 6- N -hydroxylaminopurine (6-HAP). However, in contradiction to the literature, the authors claimed that 6-HAP is nonmutagenic and proposed that the toxic effect of 6-HAP results from its ability to inhibit, in its base form, DNA synthesis. To resolve the discrepancy, we proved by genetic experiments with bacteria and yeast that extracts of MO34 do contain a mutagenic compound whose effects are identical to chemically synthesized 6-HAP. The MO34 extract induced the same mutation spectrum as authentic 6-HAP. Notably, the toxic and mutagenic effects of both synthetic and MO34-derived 6-HAP depended on conversion to the corresponding nucleotide. The nucleobase 6-HAP does not inhibit DNA synthesis in vitro, and we conclude that 6-HAP exerts its biological activity when incorporated into DNA.
机译:最近在《科学进展》上的一篇文章描述了一个惊人的发现,即共生表皮葡萄球菌菌株MO34通过产生一个被鉴定为核碱基类似物6-N-羟基氨基嘌呤(6-HAP)的小分子显示出抗菌和抗肿瘤活性。然而,与文献相反,作者声称6-HAP是非诱变的,并提出6-HAP的毒性作用是由其以其基本形式抑制DNA合成的能力引起的。为了解决这一差异,我们通过细菌和酵母菌的基因实验证明,MO34的提取物确实含有一种诱变化合物,其作用与化学合成的6-HAP相同。 MO34提取物诱导出与真实的6-HAP相同的突变谱。值得注意的是,合成的和MO34衍生的6-HAP的毒性和诱变效果都取决于转化为相应的核苷酸。核碱基6-HAP在体外不抑制DNA合成,因此我们得出结论,将6-HAP掺入DNA时会发挥其生物学活性。

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