Differential roles of two SARP-encoding regulatory genes during tylosin biosynthesis

被引:53
作者
Bate, N [1 ]
Stratigopoulos, G [1 ]
Cundliffe, E [1 ]
机构
[1] Univ Leicester, Dept Biochem, Leicester LE1 7RH, Leics, England
关键词
D O I
10.1046/j.1365-2958.2002.02756.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
The tylosin biosynthetic gene cluster of Streptomyces fradiae is remarkable in harbouring at least five regulatory genes, two of which (tylS and tylT) encode proteins of the Streptomyces antibiotic regulatory protein (SARP) family. The aim of the present work was to assess the respective contributions of TylS and TylT to tylosin production. A combination of targeted gene disruption, fermentation studies and gene expression analysis via reverse transcriptase-polymerase chain reaction (RT-PCR) suggests that tylS is essential for tylosin production and controls the expression of tylR (previously shown to be a global activator of the biosynthetic pathway) plus at least one other gene involved in polyketide metabolism or regulation thereof. This is the first demonstration of a SARP acting to control another regulatory gene during antibiotic biosynthesis. In contrast, tylT is not essential for tylosin production.
引用
收藏
页码:449 / 458
页数:10
相关论文
共 32 条
[11]   Impact of thioesterase activity on tylosin biosynthesis in Streptomyces fradiae [J].
Butler, AR ;
Bate, N ;
Cundliffe, E .
CHEMISTRY & BIOLOGY, 1999, 6 (05) :287-292
[12]  
CHATER KF, 1997, BIOTECHNOLOGY, V7, P59
[13]   THE ACT CLUSTER CONTAINS REGULATORY AND ANTIBIOTIC EXPORT GENES, DIRECT TARGETS FOR TRANSLATIONAL CONTROL BY THE BLDA TRANSFER-RNA GENE OF STREPTOMYCES [J].
FERNANDEZMORENO, MA ;
CABALLERO, JL ;
HOPWOOD, DA ;
MALPARTIDA, F .
CELL, 1991, 66 (04) :769-780
[14]   Stimulation of polyketide metabolism in Streptomyces fradiae by tylosin and its glycosylated precursors [J].
Fish, SA ;
Cundliffe, E .
MICROBIOLOGY-UK, 1997, 143 :3871-3876
[15]   CLONING GENES FOR THE BIOSYNTHESIS OF A MACROLIDE ANTIBIOTIC [J].
FISHMAN, SE ;
COX, K ;
LARSON, JL ;
REYNOLDS, PA ;
SENO, ET ;
YEH, WK ;
VANFRANK, R ;
HERSHBERGER, CL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (23) :8248-8252
[16]   STATIONARY-PHASE PRODUCTION OF THE ANTIBIOTIC ACTINORHODIN IN STREPTOMYCES-COELICOLOR A3(2) IS TRANSCRIPTIONALLY REGULATED [J].
GRAMAJO, HC ;
TAKANO, E ;
BIBB, MJ .
MOLECULAR MICROBIOLOGY, 1993, 7 (06) :837-845
[17]   Role of type II thioesterases: evidence for removal of short acyl chains produced by aberrant decarboxylation of chain extender units [J].
Heathcole, ML ;
Staunton, J ;
Leadlay, PF .
CHEMISTRY & BIOLOGY, 2001, 8 (02) :207-220
[18]  
Hopwood D.A., 1985, GENETIC MANIPULATION
[19]   DERIVATIVES OF PUC18 THAT HAVE BGLII SITES FLANKING A MODIFIED MULTIPLE CLONING SITE AND THAT RETAIN THE ABILITY TO IDENTIFY RECOMBINANT CLONES BY VISUAL SCREENING OF ESCHERICHIA-COLI COLONIES [J].
JANSSEN, GR ;
BIBB, MJ .
GENE, 1993, 124 (01) :133-134
[20]   FUNCTIONAL-CHARACTERIZATION AND TRANSCRIPTIONAL ANALYSIS OF THE DNRR(1) LOCUS, WHICH CONTROLS DAUNORUBICIN BIOSYNTHESIS IN STREPTOMYCES-PEUCETIUS [J].
MADDURI, K ;
HUTCHINSON, CR .
JOURNAL OF BACTERIOLOGY, 1995, 177 (05) :1208-1215