TY - JOUR
T1 - Mangromicins, six new anti-oxidative agents isolated from a culture broth of the actinomycete, lechevalieria aerocolonigenes K10-0216
AU - Nakashima, Takuji
AU - Kamiya, Yoshiyuki
AU - Iwatsuki, Masato
AU - Takahashi, Yoko
AU - Omura, Satoshi
N1 - Funding Information:
This study was supported, in part, by funds from Quality Assurance Framework of Higher Education from the Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan, and the Institute for Fermentation (IFO), Osaka, Japan. We are grateful to Ms Noriko Sato and Dr Kenichiro Nagai, School of Pharmacy, Kitasato University, for measurements of NMR and MS spectra and Ms Megumi Niitsuma, Kitasato Institute for Life Sciences, Kitasato University, for RT-PCR measurements.
PY - 2014/7
Y1 - 2014/7
N2 - We have been continually searching for novel chemical compounds from culture broths of various actinomycetes using a physicochemical screening system. During the course of this program, we have previously reported the discovery of two new natural products, designated mangromicins A and B, discovered in a broth of a rare actinomycete strain, Lechevalieria aerocolonigenes K10-0216. Mangromicins have a unique and rare structure, a cyclopentadecane skeleton with a tetrahydrofuran unit and a 5,6-dihydro-4- hydroxy-2-pyrone moiety. New mangromicin analogs were isolated by using an improved production medium. As a consequence, six analogs, together with mangromicins A and B, were isolated from a cultured broth of L. aerocolonigenes K10-0216. We named them mangromicins D, E, F, G, H and I. All mangromicins showed radical scavenging activities against 1,1-diphenyl-2-picrylhydrazyl (DPPH) free radicals and nitric oxide generated from LPS-stimulated RAW264.7 cells, a murine macrophage cell line. Among the analogs, mangromicins A and I showed the most potent DPPH radical scavenging activity and nitric oxide scavenging activity, respectively.
AB - We have been continually searching for novel chemical compounds from culture broths of various actinomycetes using a physicochemical screening system. During the course of this program, we have previously reported the discovery of two new natural products, designated mangromicins A and B, discovered in a broth of a rare actinomycete strain, Lechevalieria aerocolonigenes K10-0216. Mangromicins have a unique and rare structure, a cyclopentadecane skeleton with a tetrahydrofuran unit and a 5,6-dihydro-4- hydroxy-2-pyrone moiety. New mangromicin analogs were isolated by using an improved production medium. As a consequence, six analogs, together with mangromicins A and B, were isolated from a cultured broth of L. aerocolonigenes K10-0216. We named them mangromicins D, E, F, G, H and I. All mangromicins showed radical scavenging activities against 1,1-diphenyl-2-picrylhydrazyl (DPPH) free radicals and nitric oxide generated from LPS-stimulated RAW264.7 cells, a murine macrophage cell line. Among the analogs, mangromicins A and I showed the most potent DPPH radical scavenging activity and nitric oxide scavenging activity, respectively.
KW - Lechevalieria aerocolonigenes
KW - Mangromicins
KW - actinomycete strain
KW - radical scavenging activity
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U2 - 10.1038/ja.2014.34
DO - 10.1038/ja.2014.34
M3 - Article
C2 - 24690908
AN - SCOPUS:84904997642
SN - 0021-8820
VL - 67
SP - 533
EP - 539
JO - Journal of Antibiotics
JF - Journal of Antibiotics
IS - 7
ER -