Identification and in vivo functional analysis of a virginiamycin S resistance gene (varS) from Streptomyces virginiae

被引:20
作者
Lee, CK [1 ]
Kamitani, Y [1 ]
Nihira, T [1 ]
Yamada, Y [1 ]
机构
[1] Osaka Univ, Grad Sch Engn, Dept Biotechnol, Osaka 5650871, Japan
关键词
D O I
10.1128/JB.181.10.3293-3297.1999
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
BarA of Streptomyces virginiae is a specific receptor protein for virginiae butanolide (VB), one of the gamma-butyrolactone autoregulators of the Streptomyces species, and acts as a transcriptional regulator controlling both virginiamycin production and VB biosynthesis. The downstream gene barB, the transcription of which is under the tight control of the VB-BarA system, was found to be transcribed as a polycistronic mRNA with its downstream region, and DNA sequencing revealed a 1,554-bp open reading frame (ORF) beginning at 161 bp downstream of the barB termination codon. The ORF product showed high homology (68 to 73%) to drug efflux proteins having 14 transmembrane segments and was named varS (for S. virginiae antibiotic resistance). Heterologous expression of varS with S. lividans as a host resulted in virginiamycin S-specific resistance, suggesting that varS encoded a virginiamycin S-specific transport protein. Northern blot analysis indicated that the bicistronic transcript of barB-varS appeared 1 to 2 h before the onset of virginiamycin M-1 and S production, at which time Vp was produced, while exogenously added virginiamycin S apparently induced the monocistronic varS transcript.
引用
收藏
页码:3293 / 3297
页数:5
相关论文
共 23 条
  • [1] Biosynthesis of the ansamycin antibiotic rifamycin: deductions from the molecular analysis of the rif biosynthetic gene cluster of Amycolatopsis mediterranei S699
    August, PR
    Tang, L
    Yoon, YJ
    Ning, S
    Muller, R
    Yu, TW
    Taylor, M
    Hoffmann, D
    Kim, CG
    Zhang, XH
    Hutchinson, CR
    Floss, HG
    [J]. CHEMISTRY & BIOLOGY, 1998, 5 (02): : 69 - 79
  • [2] Barriere JC, 1998, CURR PHARM DESIGN, V4, P155
  • [3] THE RELATIONSHIP BETWEEN BASE COMPOSITION AND CODON USAGE IN BACTERIAL GENES AND ITS USE FOR THE SIMPLE AND RELIABLE IDENTIFICATION OF PROTEIN-CODING SEQUENCES
    BIBB, MJ
    FINDLAY, PR
    JOHNSON, MW
    [J]. GENE, 1984, 30 (1-3) : 157 - 166
  • [4] COMPUTER-ASSISTED IDENTIFICATION AND CLASSIFICATION OF STREPTOMYCETE PROMOTERS
    BOURN, WR
    BABB, B
    [J]. NUCLEIC ACIDS RESEARCH, 1995, 23 (18) : 3696 - 3703
  • [5] ORGANIZATION AND FUNCTIONS OF THE ACTVA REGION OF THE ACTINORHODIN BIOSYNTHETIC GENE-CLUSTER OF STREPTOMYCES-COELICOLOR
    CABALLERO, JL
    MARTINEZ, E
    MALPARTIDA, F
    HOPWOOD, DA
    [J]. MOLECULAR & GENERAL GENETICS, 1991, 230 (03): : 401 - 412
  • [6] SEQUENCE AND TRANSCRIPTIONAL ANALYSIS OF THE STREPTOMYCES-GLAUCESCENS TCMAR TETRACENOMYCIN-C RESISTANCE AND REPRESSOR GENE LOCI
    GUILFOILE, PG
    HUTCHINSON, CR
    [J]. JOURNAL OF BACTERIOLOGY, 1992, 174 (11) : 3651 - 3658
  • [7] Hopwood D.A., 1985, GENETIC MANIPULATION
  • [8] IDENTIFICATION OF BINDING-PROTEIN OF VIRGINIAE BUTANOLIDE-C, AN AUTOREGULATOR IN VIRGINIAMYCIN PRODUCTION, FROM STREPTOMYCES-VIRGINIAE
    KIM, HS
    NIHIRA, T
    TADA, H
    YANAGIMOTO, M
    YAMADA, Y
    [J]. JOURNAL OF ANTIBIOTICS, 1989, 42 (05) : 769 - 778
  • [9] Butyrolactone autoregulator receptor protein (BarA) as a transcriptional regulator in Streptomyces virginiae
    Kinoshita, H
    Ipposhi, H
    Okamoto, S
    Nakano, H
    Nihira, T
    Yamada, Y
    [J]. JOURNAL OF BACTERIOLOGY, 1997, 179 (22) : 6986 - 6993
  • [10] ISOLATION OF DEOXYRIBONUCLEIC ACID AND RIBOSOMAL RIBONUCLEIC ACID FROM BACTERIA
    KIRBY, KS
    FOXCARTE.E
    GUEST, M
    [J]. BIOCHEMICAL JOURNAL, 1967, 104 (01) : 258 - &