CYANOPEPTOLINS, NEW DEPSIPEPTIDES FROM THE CYANOBACTERIUM MICROCYSTIS SP PCC 7806

被引:140
|
作者
MARTIN, C
OBERER, L
INO, T
KONIG, WA
BUSCH, M
WECKESSER, J
机构
[1] ALBERT LUDWIGS UNIV,INST BIOL 2,D-79104 FREIBURG,GERMANY
[2] SANDOZ PHARMA AG,PRECLIN RES,CH-4002 BASEL,SWITZERLAND
[3] UNIV HAMBURG,INST ORGAN CHEM,D-20146 HAMBURG,GERMANY
[4] MAX PLANCK INST IMMUNBIOL,D-79108 FREIBURG,GERMANY
来源
JOURNAL OF ANTIBIOTICS | 1993年 / 46卷 / 10期
关键词
D O I
10.7164/antibiotics.46.1550
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
Four depsipeptides (peptide lactones), called cyanopeptolins A, B, C and D, have been isolated from the cyanobacterium Microcystis sp. PCC 7806. They possess identical structures consisting of cyclic L-glutamic acid-gamma-aldehyde, L-leucine, N-methyl-phenylalanine, L-valine, L-threonine, L-aspartic acid, hexanoic acid and a variable basic amino acid. This variable amino acid can be L-arginine (cyanopeptolin A), L-lysine (cyanopeptolin B), N(epsilon)-methyl-L-lysine (cyanopeptolin C) and N(epsilon),N(epsilon)-dimethyl-L-lysine (cyanopeptolin D), respectively. The L-glutamic acid-gamma-aldehyde and the amino group of L-leucine form an unusual 3-amino-6-hydroxy-2-oxo-1-piperidine system. L-Threonine is connected to L-valine via its hydroxy-group forming an ester bonding. The hexanoic acid residue is attached to the N-terminal aspartic acid residue which is not a part of the ring structure. The isolation procedure of the four cyanopeptolins as well as structure elucidation are described. Amino acid analysis, GC/MS analysis, FAB-MS and several NMR techniques were used to reveal the structures.
引用
收藏
页码:1550 / 1556
页数:7
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