TY - JOUR
T1 - Unsaturated fatty acids and a prenylated tryptophan derivative from a rare actinomycete of the genus Couchioplanes
AU - Saito, Shun
AU - Indo, Kanji
AU - Oku, Naoya
AU - Komaki, Hisayuki
AU - Kawasaki, Masashi
AU - Igarashi, Yasuhiro
N1 - Funding Information:
This work was supported by JSPS KAKENHI Grant Number 19K05848 to Y. I.
Publisher Copyright:
© 2021 Beilstein-Institut Zur Forderung der Chemischen Wissenschaften. All rights reserved.
PY - 2021
Y1 - 2021
N2 - A genome mining survey combined with metabolome analysis of publicly available strains identified Couchioplanes sp. RD010705, a strain belonging to an underexplored genus of rare actinomycetes, as a producer of new metabolites. HPLC-DADguided fractionation of its fermentation extracts resulted in the isolation of five new methyl-branched unsaturated fatty acids, (2E,4E)-2,4-dimethyl-2,4-octadienoic acid (1), (2E,4E)-2,4,7-trimethyl-2,4-octadienoic acid (2), (R)-(-)-phialomustin B (3), (2E,4E)-7-hydroxy-2,4-dimethyl-2,4-octadienoic acid (4), (2E,4E)-7-hydroxy-2,4,7-trimethyl-2,4-octadienoic acid (5), and one prenylated tryptophan derivative, 6-(3,3-dimethylallyl)-N-acetyl-L-tryptophan (6). The enantiomer ratio of 4 was determined to be approximately S/R = 56:44 by a recursive application of Trost's chiral anisotropy analysis and chiral HPLC analysis of its methyl ester. Compounds 1-5 were weakly inhibitory against Kocuria rhizophila at MIC 100 μg/mL and none were cytotoxic against P388 at the same concentration.
AB - A genome mining survey combined with metabolome analysis of publicly available strains identified Couchioplanes sp. RD010705, a strain belonging to an underexplored genus of rare actinomycetes, as a producer of new metabolites. HPLC-DADguided fractionation of its fermentation extracts resulted in the isolation of five new methyl-branched unsaturated fatty acids, (2E,4E)-2,4-dimethyl-2,4-octadienoic acid (1), (2E,4E)-2,4,7-trimethyl-2,4-octadienoic acid (2), (R)-(-)-phialomustin B (3), (2E,4E)-7-hydroxy-2,4-dimethyl-2,4-octadienoic acid (4), (2E,4E)-7-hydroxy-2,4,7-trimethyl-2,4-octadienoic acid (5), and one prenylated tryptophan derivative, 6-(3,3-dimethylallyl)-N-acetyl-L-tryptophan (6). The enantiomer ratio of 4 was determined to be approximately S/R = 56:44 by a recursive application of Trost's chiral anisotropy analysis and chiral HPLC analysis of its methyl ester. Compounds 1-5 were weakly inhibitory against Kocuria rhizophila at MIC 100 μg/mL and none were cytotoxic against P388 at the same concentration.
KW - Couchioplanes
KW - Prenylated tryptophan
KW - Rare actinomycete
KW - Unsaturated fatty acid
UR - http://www.scopus.com/inward/record.url?scp=85122340944&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85122340944&partnerID=8YFLogxK
U2 - 10.3762/bjoc.17.203
DO - 10.3762/bjoc.17.203
M3 - Article
AN - SCOPUS:85122340944
SN - 1860-5397
VL - 17
SP - 2939
EP - 2949
JO - Beilstein Journal of Organic Chemistry
JF - Beilstein Journal of Organic Chemistry
ER -