The tylosin biosynthetic cluster from Streptomyces fradiae:: genetic organization of the left region

被引:91
作者
Fouces, R [1 ]
Mellado, E [1 ]
Díez, B [1 ]
Barredo, JL [1 ]
机构
[1] Antibiot SA, Lab Ingn Genet, Leon 24080, Spain
来源
MICROBIOLOGY-UK | 1999年 / 145卷
关键词
glycosyltransferase; ketoreductase; cytochrome P450; methyltransferase; mycinose;
D O I
10.1099/13500872-145-4-855
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The genetic organization of the left edge (tylEDHFJ region) of the tylosin biosynthetic gene cluster from Streptomyces fradiae has been determined. Sequence analysis of a 12 9 kb region has revealed the presence of 11 ORFs, 10 of them belonging to the biosynthetic cluster. The putative functions of the proteins encoded by these genes are as follows: peptidase (ORF1, ddcA), tylosin resistance determinant (ORF2, tlrB), glycosyltransferase (ORF3, tylN), methyltransferase (ORF4, tylE), ketoreductase (ORF5, tylD), ferredoxin (ORF6, tylH2), cytochrome P450 (ORF7, tylH1), methyltransferase (ORF8, tylF), epimerase (ORF9, tylJ), acyl-CoA oxidase (ORF10, tylP) and receptor of regulatory factors (ORF11, tylQ). The functional identification of the genes in the proposed tylosin biosynthetic pathway has been deduced by database searches and previous genetic complementation studies performed with tylosin idiotrophic mutants blocked at various stages in tylosin biosynthesis. The tlrB gene has been shown to be useful as a tylosin resistance marker in Streptomyces lividans, Streptomyces parvulus and Streptomyces coelicolor and the effect of tylF on macrocin depletion has been confirmed. A pathway for the biosynthesis of B-deoxy-D-allose, the unmethylated mycinose precursor, involving the genes tylD, tylJ and tylN is proposed.
引用
收藏
页码:855 / 868
页数:14
相关论文
共 74 条
[1]   An alkaline D-stereospecific endopeptidase with beta-lactamase activity from Bacillus cereus [J].
Asano, Y ;
Ito, H ;
Dairi, T ;
Kato, Y .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (47) :30256-30262
[2]   PROPERTIES OF STREPTOMYCES-FRADIAE MUTANTS BLOCKED IN BIOSYNTHESIS OF THE MACROLIDE ANTIBIOTIC TYLOSIN [J].
BALTZ, RH ;
SENO, ET .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1981, 20 (02) :214-225
[3]   BIOSYNTHESIS OF THE MACROLIDE ANTIBIOTIC TYLOSIN - A PREFERRED PATHWAY FROM TYLACTONE TO TYLOSIN [J].
BALTZ, RH ;
SENO, ET ;
STONESIFER, J ;
WILD, GM .
JOURNAL OF ANTIBIOTICS, 1983, 36 (02) :131-141
[4]  
BALTZ RH, 1988, ANNU REV MICROBIOL, V42, P547
[5]   Applications of transposition mutagenesis in antibiotic producing streptomycetes [J].
Baltz, RH ;
McHenney, MA ;
Cantwell, CA ;
Queener, SW ;
Solenberg, PJ .
ANTONIE VAN LEEUWENHOEK INTERNATIONAL JOURNAL OF GENERAL AND MOLECULAR MICROBIOLOGY, 1997, 71 (1-2) :179-187
[6]  
BALTZ RH, 1995, GENE EXPRESSION RECO, P309
[7]   THE MOLECULAR-STRUCTURE OF UDP-GALACTOSE 4-EPIMERASE FROM ESCHERICHIA-COLI DETERMINED AT 2.5 A-RESOLUTION [J].
BAUER, AJ ;
RAYMENT, I ;
FREY, PA ;
HOLDEN, HM .
PROTEINS-STRUCTURE FUNCTION AND GENETICS, 1992, 12 (04) :372-381
[8]  
BAUER NJ, 1988, J BIOL CHEM, V263, P15619
[9]  
BECKMANN RJ, 1989, GENETICS MOL BIOL IN, P176
[10]   THE RELATIONSHIP BETWEEN BASE COMPOSITION AND CODON USAGE IN BACTERIAL GENES AND ITS USE FOR THE SIMPLE AND RELIABLE IDENTIFICATION OF PROTEIN-CODING SEQUENCES [J].
BIBB, MJ ;
FINDLAY, PR ;
JOHNSON, MW .
GENE, 1984, 30 (1-3) :157-166