REGULATION OF EPIDERMIN BIOSYNTHETIC GENES BY EPIQ

被引:76
作者
PESCHEL, A [1 ]
AUGUSTIN, J [1 ]
KUPKE, T [1 ]
STEVANOVIC, S [1 ]
GOTZ, F [1 ]
机构
[1] UNIV TUBINGEN,MORGENSTELLE 28,W-7400 TUBINGEN 1,GERMANY
关键词
D O I
10.1111/j.1365-2958.1993.tb01666.x
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
We investigated the role of epiQ in the biosynthesis of the lantibiotic epidermin. epiQ was essential for epidermin production. It was shown that EpiQ controls epidermin production by transcriptionally activating the epiA promoter, used for transcription of most of the epidermin biosynthetic genes. Additional copies of epiQ increased epidermin production in the epidermin-producing wild-type strain Staphylococcus epidermidis Tu3298. The epiA promoter region was characterized by primer extension analysis. Two inverted repeats, putative operator sites for EpiQ binding, are located upstream of the -35 region and one is localized downstream of the -10 region. Crude protein extracts from S. epidermidis Tu3298 and epiQ expressing Escherichia coli cells led to gel mobility shifts of a DNA fragment bearing the inverted repeat which is located immediately upstream of the -35 region. DNA fragments bearing the other two inverted repeats were not shifted. The epiQ gene product could be detected by overexpression in the E. coli T7 system using antiserum raised against synthetic peptides of EpiQ. Furthermore, EpiQ, like other DNA-binding proteins, was shown to bind strongly to heparin sepharose.
引用
收藏
页码:31 / 39
页数:9
相关论文
共 36 条
  • [1] ELUCIDATION OF THE STRUCTURE OF EPIDERMIN, A RIBOSOMALLY SYNTHESIZED, TETRACYCLIC HETERODETIC POLYPEPTIDE ANTIBIOTIC
    ALLGAIER, H
    JUNG, G
    WERNER, RG
    SCHNEIDER, U
    ZAHNER, H
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 1985, 24 (12) : 1051 - 1053
  • [2] EPIDERMIN - SEQUENCING OF A HETERODET TETRACYCLIC 21-PEPTIDE AMIDE ANTIBIOTIC
    ALLGAIER, H
    JUNG, G
    WERNER, RG
    SCHNEIDER, U
    ZAHNER, H
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1986, 160 (01): : 9 - 22
  • [3] GENETIC-ANALYSIS OF EPIDERMIN BIOSYNTHETIC GENES AND EPIDERMIN-NEGATIVE MUTANTS OF STAPHYLOCOCCUS-EPIDERMIDIS
    AUGUSTIN, J
    ROSENSTEIN, R
    WIELAND, B
    SCHNEIDER, U
    SCHNELL, N
    ENGELKE, G
    ENTIAN, KD
    GOTZ, F
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1992, 204 (03): : 1149 - 1154
  • [4] AUGUSTIN J, 1990, FEMS MICROBIOL LETT, V66, P203, DOI 10.1016/0378-1097(90)90283-V
  • [5] CONSTRUCTION AND CHARACTERIZATION OF AMPLIFIABLE MULTICOPY DNA CLONING VEHICLES DERIVED FROM P15A CRYPTIC MINIPLASMID
    CHANG, ACY
    COHEN, SN
    [J]. JOURNAL OF BACTERIOLOGY, 1978, 134 (03) : 1141 - 1156
  • [6] CONTROL SITE LOCATION AND TRANSCRIPTIONAL REGULATION IN ESCHERICHIA-COLI
    COLLADOVIDES, J
    MAGASANIK, B
    GRALLA, JD
    [J]. MICROBIOLOGICAL REVIEWS, 1991, 55 (03) : 371 - 394
  • [7] DECROMBRUGGHE B, 1984, BIOL REGUL DEV, V3, P129
  • [8] HIGH-EFFICIENCY TRANSFORMATION OF ESCHERICHIA-COLI BY HIGH-VOLTAGE ELECTROPORATION
    DOWER, WJ
    MILLER, JF
    RAGSDALE, CW
    [J]. NUCLEIC ACIDS RESEARCH, 1988, 16 (13) : 6127 - 6145
  • [9] BIOSYNTHESIS OF THE LANTIBIOTIC NISIN - GENOMIC ORGANIZATION AND MEMBRANE LOCALIZATION OF THE NISB PROTEIN
    ENGELKE, G
    GUTOWSKIECKEL, Z
    HAMMELMANN, M
    ENTIAN, KD
    [J]. APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1992, 58 (11) : 3730 - 3743
  • [10] IMPROVEMENTS OF PROTOPLAST TRANSFORMATION IN STAPHYLOCOCCUS-CARNOSUS
    GOTZ, F
    SCHUMACHER, B
    [J]. FEMS MICROBIOLOGY LETTERS, 1987, 40 (2-3) : 285 - 288