Kanchanamycins, new polyol macrolide antibiotics produced by Streptomyces olivaceus Tu 4018 .2. Structure elucidation

被引:14
|
作者
Stephan, H
Kempter, C
Metzger, JW
Jung, G
Potterat, O
Pfefferle, C
Fiedler, HP
机构
[1] UNIV LAUSANNE,INST PHARMACOGNOSIE & PHYTOCHIM,CH-1015 LAUSANNE,SWITZERLAND
[2] UNIV TUBINGEN,INST BIOL,D-72076 TUBINGEN,GERMANY
来源
JOURNAL OF ANTIBIOTICS | 1996年 / 49卷 / 08期
关键词
D O I
10.7164/antibiotics.49.765
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
Kanchanamycins are a new group of polyol macrolide antibiotics isolated from Streptomyces olivaceus Tu 4018. They all share a common bicyclic carbon skeleton formed by a 36-membered lactone ring and a 6-membered hemiacetal ring. A feature unusual for that class of macrolides is the terminal urea moiety observed in kanchanamycin A. The structures of the kanchanamycins were determined by electrospray MS and modern 2D NMR techniques. Due to substantial overlap of the signals intensive use of inverse detected heteronuclear correlation experiments (HSQC, HMBC, 2D-HSQC-TOCSY) was made.
引用
收藏
页码:765 / 769
页数:5
相关论文
共 50 条
  • [1] Kanchanamycins, new polyol macrolide antibiotics produced by Streptomyces olivaceus Tu 4018 .1. Taxonomy, fermentation, isolation and biological activities
    Fiedler, HP
    Nega, M
    Pfefferle, C
    Groth, I
    Kempter, C
    Stephan, H
    Metzger, JW
    JOURNAL OF ANTIBIOTICS, 1996, 49 (08): : 758 - 764
  • [2] Dihydroniphimycin:: New polyol macrolide antibiotic produced by Streptomyces hygroscopicus 15 -: Isolation and structure elucidation
    Ivanova, V
    Gesheva, V
    Kolarova, M
    JOURNAL OF ANTIBIOTICS, 2000, 53 (06): : 627 - 632
  • [3] ELUCIDATION OF STRUCTURE OF NOVEL MACROLIDE ANTIBIOTICS PRODUCED BY MUTANT STRAINS OF STREPTOMYCES-FRADIAE
    KIRST, HA
    WILD, GM
    BALTZ, RH
    SENO, ET
    HAMILL, RL
    PASCHAL, JW
    DORMAN, DE
    JOURNAL OF ANTIBIOTICS, 1983, 36 (04): : 376 - 382
  • [4] (E)4-Oxonon-2-enoic acid, an antibiotically active fatty acid produced by Streptomyces olivaceus Tu 4018
    Pfefferle, C
    Kempter, C
    Metzger, JW
    Fiedler, HP
    JOURNAL OF ANTIBIOTICS, 1996, 49 (08): : 826 - 828
  • [5] NANAOMYCINS, NEW ANTIBIOTICS PRODUCED BY A STRAIN OF STREPTOMYCES .2. STRUCTURE AND BIOSYNTHESIS
    TANAKA, H
    KOYAMA, Y
    NAGAI, T
    MARUMO, H
    OMURA, S
    JOURNAL OF ANTIBIOTICS, 1975, 28 (11): : 868 - 875
  • [6] SWALPAMYCIN, A NEW MACROLIDE ANTIBIOTIC .2. STRUCTURE ELUCIDATION
    CHATTERJEE, S
    REDDY, GCS
    FRANCO, CMM
    RUPP, RH
    GANGULI, BN
    FEHLHABER, HW
    KOGLER, H
    JOURNAL OF ANTIBIOTICS, 1987, 40 (10): : 1368 - 1374
  • [7] Arylomycins A and B, new biaryl-bridged lipopeptide antibiotics produced by Streptomyces sp Tu 6075 -: II.: Structure elucidation
    Höltzel, A
    Schmid, DG
    Nicholson, GJ
    Stevanovic, S
    Schimana, J
    Gebhardt, K
    Fiedler, HP
    Jung, G
    JOURNAL OF ANTIBIOTICS, 2002, 55 (06): : 571 - 577
  • [8] Streptocidinis A∼D, novel cyclic decapeptide antibiotics produced by Streptomyces sp Tu 6071 II.: Structure elucidation
    Höltzel, A
    Jack, RW
    Nicholson, GJ
    Jung, G
    Gebhardt, K
    Fiedler, HP
    Süssmuth, RD
    JOURNAL OF ANTIBIOTICS, 2001, 54 (05): : 434 - 440
  • [9] Simocyclinones, novel cytostatic angucyclinone antibiotics produced by Streptomyces antibioticus Tu 6040 -: II.: Structure elucidation and biosynthesis
    Holzenkämpfer, M
    Walker, M
    Zeeck, A
    Schimana, J
    Fiedler, HP
    JOURNAL OF ANTIBIOTICS, 2002, 55 (03): : 301 - 307
  • [10] A NEW MEMBER OF THE CLASS OF ANTIBIOTICS WITH THIOTETRONIC ACID STRUCTURE ISOLATED FROM STREPTOMYCES-OLIVACEUS TU-3010
    RAPP, C
    JUNG, G
    ISSELHORSTSCHARR, C
    ZAHNER, H
    LIEBIGS ANNALEN DER CHEMIE, 1988, (11): : 1043 - 1047