1. [Secondary metabolites from a deep-sea-derived actinomycete Micrococcus sp. R21].
- Author
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Peng K, Su RQ, Zhang GY, Cheng XX, Yang Q, Liu YH, and Yang XW
- Subjects
- Animals, Biological Factors isolation & purification, Biological Factors metabolism, Biological Factors pharmacology, Cell Survival drug effects, Macrophages cytology, Macrophages drug effects, Magnetic Resonance Spectroscopy, Mass Spectrometry, Mice, Micrococcus genetics, Micrococcus isolation & purification, Molecular Structure, Phylogeny, RAW 264.7 Cells, Biological Factors chemistry, Micrococcus chemistry, Micrococcus metabolism, Seawater microbiology, Secondary Metabolism
- Abstract
To investigate cytotoxic secondary metabolites of Micrococcus sp. R21, an actinomycete isolated from a deep-sea sediment (-6 310 m; 142 degrees 19. 9' E, 10 degrees 54. 6' N) of the Western Pacific Ocean, column chromatography was introduced over silica gel, ODS, and Sephadex LH-20. As a result, eight compounds were obtained. By mainly detailed analysis of the NMR data, their structures were elucidated as cyclo(4-hydroxy-L-Pro-L-leu) (1), cyclo(L-Pro-L-Gly) (2), cyclo( L-Pro-L-Ala) (3), cyclo( D-Pro-L-Leu) (4), N-β-acetyltryptamine (5), 2-hydroxybenzoic acid (6), and phenylacetic acid (7). Compound 1 exhibited weak cytotoxic activity against RAW264. 7 cells with IC50 value of 9.1 μmol x L(-1).
- Published
- 2015