| Literature DB >> 28202308 |
Takuji Nakashima1, Toru Kimura2, Rei Miyano2, Hirotaka Matsuo3, Tomoyasu Hirose4, Aoi Kimishima2, Kenichi Nonaka4, Masato Iwatsuki4, Jun Nakanishi5, Yōko Takahashi3, Satoshi Ōmura3.
Abstract
Physicochemical screening identified a new nanaomycin analog, nanaomycin H, which was isolated from a culture broth of Streptomyces rosa subsp. notoensis OS-3966. This microorganism is already known to produce seven nanaomycin compounds, (nanaomycin A to G). Structural elucidation of nanaomycin H showed it to be a pyranonaphthoquinone with a mycothiol moiety. A N-acetylcysteine S-conjugate of nanaomycin H, without α-glucosamine linked to myo-inositol moiety, mercapturic acid derivative, was also detected in the same culture broth. Mercapturic acid derivatives of secondary metabolites are known to be produced for xenobiotic metabolism outside microbial cells. Mycothiol acts as a detoxifier to help prevent cell damage from factors such as oxidative stress. The production of O2- generated by reduction of nanaomycin A is correlated with antibacterial activity. Mycothiol-containing nanaomycin H proved to be markedly decreased in O2- and did not express any notable antimicrobial activity. It is suggested that nanaomycin H is produced in the detoxification process.Entities:
Keywords: Nanaomycin H; New nanaomycin analog; Physicochemical screening; Streptomyces spp.
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Year: 2017 PMID: 28202308 DOI: 10.1016/j.jbiosc.2017.01.011
Source DB: PubMed Journal: J Biosci Bioeng ISSN: 1347-4421 Impact factor: 2.894