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Merck
CN
  • Genotype-driven isolation of enterocin with novel bioactivities from mangrove-derived Streptomyces qinglanensis 172205.

Genotype-driven isolation of enterocin with novel bioactivities from mangrove-derived Streptomyces qinglanensis 172205.

Applied microbiology and biotechnology (2015-04-22)
Dong-Bo Xu, Min Ma, Zi-Xin Deng, Kui Hong
摘要

The type II polyketide synthase (PKS) natural product enterocin (1) was isolated from a mangrove-derived novel species Streptomyces qinglanensis 172205 guided by genome sequence, and its putative biosynthetic gene cluster was revealed. Its natural analogues 5-deoxyenterocin (2) and wailupemycin A-C (3-5) were also identified by tandem mass spectrometry. By feeding experiments with aryl acids, strain 172205 was proved to incorporate partial exogenous starter units into enterocin- and wailupemycin-based analogues, thus being a new and suitable microorganism for engineering unnatural enc-derived polyketide metabolites. In addition, biological assays indicated that enterocin showed obvious inhibitory activity against β-amyloid protein (Aβ1-42) fibrillation and moderate cytotoxicity against HeLa and HepG2 for the first time.

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Sigma-Aldrich
乙酸乙酯, anhydrous, 99.8%
Sigma-Aldrich
硫代磺素T, used as stain for amyloid
Sigma-Aldrich
淀粉样蛋白β蛋白片段1-42
Sigma-Aldrich
乙酸乙酯, ≥99%, FCC, FG
Sigma-Aldrich
4-硝基苯基 β-D-葡糖苷酸, ≥98% (TLC)
Sigma-Aldrich
乙酸乙酯, natural, ≥99%, FCC, FG
Sigma-Aldrich
乙酸乙酯, ReagentPlus®, ≥99.8%
Sigma-Aldrich
4-硝基苯基 β-D-葡糖苷酸, ≥99.0% (TLC)
Sigma-Aldrich
3-(Benzyldimethylammonio)propanesulfonate, BioXtra, ≥99.0% (HPCE)
Sigma-Aldrich
Enterocin, ≥95% (HPLC)