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Comment on “A commensal strain ofStaphylococcus epidermidisprotects against skin neoplasia” by Nakatsujiet al.
Author(s) -
Stanislav G. Kozmin,
Igor B. Rogozin,
Elizabeth A. Moore,
Mariah Abney,
Roel M. Schaaper,
Youri I. Pavlov
Publication year - 2019
Publication title -
science advances
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.928
H-Index - 146
ISSN - 2375-2548
DOI - 10.1126/sciadv.aaw3915
Subject(s) - staphylococcus epidermidis , strain (injury) , microbiology and biotechnology , staphylococcus aureus , staphylococcus , biology , medicine , bacteria , genetics , anatomy
A recent article in described the striking discovery that the commensal strain MO34 displays antimicrobial and antitumor activities by producing a small molecule, identified as the nucleobase analog 6--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.

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