ISOLATION ON TREHALAMINE, THE AGLYCON OF TREHAZOLIN, FROM MICROBIAL BROTHS AND CHARACTERIZATION OF TREHAZOLIN RELATED-COMPOUNDS

被引:40
作者
ANDO, O
NAKAJIMA, M
HAMANO, K
ITOI, K
TAKAHASHI, S
TAKAMATSU, Y
SATO, A
ENOKITA, R
OKAZAKI, T
HARUYAMA, H
KINOSHITA, T
机构
[1] SANKYO CO LTD, FERMENTAT RES LABS, 1-2-58 HIROMACHI, SHINAGAWA KU, TOKYO 140, JAPAN
[2] SANKYO CO LTD, TSUKUBA RES LABS, TSUKUBA, IBARAKI 305, JAPAN
[3] SANKYO CO LTD, ANALYT & METAB RES LABS, SHINAGAWA KU, TOKYO 140, JAPAN
关键词
D O I
10.7164/antibiotics.46.1116
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Trehalamine, (3aR,4R,5S,6S,6aS)-2-amino-4-(hydroxymethyl)-3a,5,6,6a-tetrahydro-4H-cyclo-pent[d]oxazole-4,5,6-triol (1) and D-glucose were obtained by acid hydrolysis of trehazolin (3), a trehalase inhibitor produced by actinomycetes. More vigorous hydrolytic treatment of trehazolin afforded an aminocyclitol, (1R,2S,3R,4S,5R)-5-amino-1-(hydroxymethyl)cyclopentane-1,2,3,4-tetraol (2). Trehalamine, the aglycon of trehazolin, was also found in the culture broths of two trehazolin producing strains, Micromonospora sp. SANK 62390 and Amycolatopsis sp. SANK 60791. These trehazolin related compounds trehalamine (1) and 2 were poor inhibitors of trehalase (1; IC50 1.8 x 10(-4) m, 2; > 5.0 x 10(-4) m). On the other hand they inhibited more potently rat intestinal sucrase (1; IC50 6.8 x 10(-5) m) and sweet almond beta-glucosidase (2; IC50 5.6 x 10(-6) m) than trehazolin.
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页码:1116 / 1125
页数:10
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