Preparation of Site-Specific Isotopically Labelled Zervamicins, the Antibiotic Peptaibols Produced by Emericellopsis Salmosynnemata

被引:11
作者
Egorova-Zachernyuk, T. A. [1 ]
Shvets, V. I. [1 ]
Versluis, K. [2 ]
Heerma, W. [2 ]
Creemers, A. F. L. [3 ]
Nieuwenhuis, S. A. M. [3 ]
Lugtenburg, J. [3 ]
Raap, J. [3 ]
机构
[1] MV Lomonosov Moscow State Acad Fine Chem Technol, Moscow, Russia
[2] Univ Utrecht, Bijvoet Ctr Biomol Res, NL-3508 TC Utrecht, Netherlands
[3] Leiden Univ, Leiden Inst Chem, NL-2300 RA Leiden, Netherlands
关键词
Biosynthesis; deuterium; nitrogen; 15; positive ion FAB mass spectrometry; ion channel-forming peptide;
D O I
10.1002/psc.72
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A simple procedure for the preparation of the specifically labelled peptide antibiotic zervamicins IC, IIA and IIB has been developed. The zervamicin molecules are labelled with stable isotopes by culturing the Emericebpsis salmosynnemata on a well-defined synthetic medium containing the highly isotopically enriched amino acid. To obtain the peptide with the specifically and highly enriched amino acid residue, precautions have been taken to prevent any de mu0 biosynthesis of the particular amino acid from unlabelled precursors. The enrichment of the labelled peptide is determined by mass spectrometric analysis. Following this method we have incorporated [2`, 4', 5', 6'. 7'-H-2(5),]-L-[-1'-N-15] -L-T1r apn-d [2', 3', 4', 5', 6'-H-2(5)]-L--Phl16 into zervamicins IC, IIA and IIB on the preparative scale and without scrambling of the label. Thus, using the procedures described, isotopically labelled zervamicins can be prepared, allowing them to be studied by solid-state NMR.
引用
收藏
页码:341 / 350
页数:10
相关论文
共 22 条
  • [1] ZERVAMICINS, A STRUCTURALLY CHARACTERIZED PEPTIDE MODEL FOR MEMBRANE ION CHANNELS
    AGARWALLA, S
    MELLOR, IR
    SANSOM, MSP
    KARLE, IL
    FLIPPENANDERSON, JL
    UMA, K
    KRISHNA, K
    SUKUMAR, M
    BALARAM, P
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 186 (01) : 8 - 15
  • [2] ARGOUDELIS A, 1975, Patent No. 3907990
  • [3] ZERVAMICINS I AND II, POLYPEPTIDE ANTIBIOTICS PRODUCED BY EMERICELLOPSIS-SALMOSYNNEMATA
    ARGOUDELIS, AD
    DIETZ, A
    JOHNSON, LE
    [J]. JOURNAL OF ANTIBIOTICS, 1974, 27 (05) : 321 - 328
  • [4] BALARAM P, 1992, EUR BIOPHYS J BIOPHY, V21, P117, DOI 10.1007/BF00185426
  • [5] PEPTAIBOL ANTIBIOTICS - A STUDY ON THE HELICAL STRUCTURE OF THE 2-9 SEQUENCE OF EMERIMICIN-III AND EMERIMICIN-IV
    BENEDETTI, E
    BAVOSO, A
    DIBLASIO, B
    PAVONE, V
    PEDONE, C
    TONIOLO, C
    BONORA, GM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-PHYSICAL SCIENCES, 1982, 79 (24): : 7951 - 7954
  • [6] FTIR SPECTROSCOPY SHOWS WEAK SYMMETRICAL HYDROGEN-BONDING OF THE Q(B) CARBONYL GROUPS IN RHODOBACTER-SPHAEROIDES R26 REACTION CENTERS
    BRUDLER, R
    DEGROOT, HJM
    VANLIEMT, WBS
    GAST, P
    HOFF, AJ
    LUGTENBURG, J
    GERWERT, K
    [J]. FEBS LETTERS, 1995, 370 (1-2) : 88 - 92
  • [7] C-13 MAGIC ANGLE SPINNING NMR-STUDY OF THE LIGHT-INDUCED AND TEMPERATURE-DEPENDENT CHANGES IN RHODOBACTER-SPHAEROIDES R26 REACTION CENTERS ENRICHED IN [4'-C-13]TYROSINE
    FISCHER, MR
    DEGROOT, HJM
    RAAP, J
    WINKEL, C
    HOFF, AJ
    LUGTENBURG, J
    [J]. BIOCHEMISTRY, 1992, 31 (45) : 11038 - 11049
  • [8] TRYPTOPHANS IN MEMBRANE-PROTEINS - INDOLE RING ORIENTATIONS AND FUNCTIONAL IMPLICATIONS IN THE GRAMICIDIN CHANNEL
    HU, W
    LEE, KC
    CROSS, TA
    [J]. BIOCHEMISTRY, 1993, 32 (27) : 7035 - 7047
  • [9] Karle I. L., 1992, STRUCTURE FUNCTION, V2, P97
  • [10] CRYSTAL-STRUCTURE OF [LEU1]ZERVAMICIN, A MEMBRANE ION-CHANNEL PEPTIDE - IMPLICATIONS FOR GATING MECHANISMS
    KARLE, IL
    FLIPPENANDERSON, JL
    AGARWALLA, S
    BALARAM, P
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (12) : 5307 - 5311