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
[51]   METABOLIC PRODUCTS OF MICROORGANISMS .113. BIOSYNTHESIS OF THYMIDINE DIPHOSPHO MYCAROSE IN A CELL-FREE SYSTEM FROM STREPTOMYCES-RIMOSUS [J].
PAPE, H ;
BRILLINGER, GU .
ARCHIV FUR MIKROBIOLOGIE, 1973, 88 (01) :25-35
[52]   GENETICS OF STREPTOMYCIN PRODUCTION IN STREPTOMYCES-GRISEUS - MOLECULAR-STRUCTURE AND PUTATIVE FUNCTION OF GENES STRELMB2N [J].
PISSOWOTZKI, K ;
MANSOURI, K ;
PIEPERSBERG, W .
MOLECULAR & GENERAL GENETICS, 1991, 231 (01) :113-123
[53]   HIGH-RESOLUTION CRYSTAL-STRUCTURE OF CYTOCHROME-P450CAM [J].
POULOS, TL ;
FINZEL, BC ;
HOWARD, AJ .
JOURNAL OF MOLECULAR BIOLOGY, 1987, 195 (03) :687-700
[54]   A NEW SHUTTLE COSMID VECTOR, PKC505, FOR STREPTOMYCETES - ITS USE IN THE CLONING OF 3 DIFFERENT SPIRAMYCIN-RESISTANCE GENES FROM A STREPTOMYCES-AMBOFACIENS LIBRARY [J].
RICHARDSON, MA ;
KUHSTOSS, S ;
SOLENBERG, P ;
SCHAUS, NA ;
RAO, RN .
GENE, 1987, 61 (03) :231-241
[55]   POLYKETIDE SYNTHASE COMPLEXES - THEIR STRUCTURE AND FUNCTION IN ANTIBIOTIC BIOSYNTHESIS [J].
ROBINSON, JA .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES, 1991, 332 (1263) :107-114
[56]   HOMOLOGY BETWEEN PROTEINS CONTROLLING STREPTOMYCES-FRADIAE TYLOSIN RESISTANCE AND ATP-BINDING TRANSPORT [J].
ROSTECK, PR ;
REYNOLDS, PA ;
HERSHBERGER, CL .
GENE, 1991, 102 (01) :27-32
[57]  
Salah-Bey K, 1998, MOL GEN GENET, V257, P542
[58]  
Sambrook J., 1989, MOL CLONING LAB MANU
[59]   ACTINOMYCETE CYTOCHROMES P-450 INVOLVED IN OXIDATIVE-METABOLISM - BIOCHEMISTRY AND MOLECULAR-BIOLOGY [J].
SARIASLANI, FS ;
OMER, CA .
CRITICAL REVIEWS IN PLANT SCIENCES, 1992, 11 (01) :1-16
[60]   PROPERTIES OF S-ADENOSYL-L-METHIONINE-MACROCIN OMICRON-METHYLTRANSFERASE IN EXTRACTS OF STREPTOMYCES-FRADIAE STRAINS WHICH PRODUCE NORMAL OR ELEVATED LEVELS OF TYLOSIN AND IN MUTANTS BLOCKED IN SPECIFIC OMICRON-METHYLATIONS [J].
SENO, ET ;
BALTZ, RH .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1981, 20 (03) :370-377