Biosynthesis of elloramycin in Streptomyces olivaceus requires glycosylation by enzymes encoded outside the aglycon cluster

被引:36
作者
Ramos, Angelina [1 ,2 ]
Lombo, Felipe [1 ,2 ]
Brana, Alfredo F. [1 ,2 ]
Rohr, Juergen [3 ]
Mendez, Carmen [1 ,2 ]
Salas, Jose A. [1 ,2 ]
机构
[1] Univ Oviedo, Dept Biol Func, E-33006 Oviedo, Spain
[2] Univ Oviedo, IUOPA, E-33006 Oviedo, Spain
[3] Univ Kentucky, Coll Pharm, Dept Pharmaceut Sci, Lexington, KY 40536 USA
来源
MICROBIOLOGY-SGM | 2008年 / 154卷
关键词
D O I
10.1099/mic.0.2007/014035-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Elloramycin is an anthracycline-like antitumour drug produced by Streptomyces olivaceus Tu2353. Cosmid cos16F4 has been previously shown to direct the biosynthesis of the elloramycin aglycon 8-demethyltetracenomycin C (8-DMTC), but not elloramycin. Sequencing of the 24.2 kb insert in cos16F4 shows the presence of 17 genes involved in elloramycin biosynthesis (elm genes) together with another additional eight ORFs probably not involved in elloramycin biosynthesis. The 17 genes would code for the biosynthesis of the polyketide moiety, sugar transfer, methylation of the tetracyclic ring and the sugar moiety, and export. Four genes (rhaA, rhaB, rhaC and rhaD) encoding the enzymic activities required for the biosynthesis of the sugar L-rhamnose were also identified in the S. olivaceus chromosome. The involvement of this rhamnose gene cluster in elloramycin biosynthesis was demonstrated by insertional inactivation of the rhaB gene, generating a non-producer mutant that accumulates the 8-DMTC C aglycon. Coexpression of cos16F4 with pEM4RO (expressing the four rhamnose biosynthesis genes) in Streptomyces lividans led to the formation of elloramycin, demonstrating that both subclusters are required for elloramycin biosynthesis. These results demonstrate that, in contrast to most of the biosynthesis gene clusters from actinomycetes, genes involved in the biosynthesis of elloramycin are located in two chromosomal loci.
引用
收藏
页码:781 / 788
页数:8
相关论文
共 32 条
[1]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[2]  
[Anonymous], 2000, Practical Streptomyces genetics, DOI DOI 10.1111/J.1365-2427.2007.01876.X
[3]   ANALYSIS OF THE NUCLEOTIDE-SEQUENCE OF THE STREPTOMYCES-GLAUCESCENS TCML GENES PROVIDES KEY INFORMATION ABOUT THE ENZYMOLOGY OF POLYKETIDE ANTIBIOTIC BIOSYNTHESIS [J].
BIBB, MJ ;
BIRO, S ;
MOTAMEDI, H ;
COLLINS, JF ;
HUTCHINSON, CR .
EMBO JOURNAL, 1989, 8 (09) :2727-2736
[4]   PLASMID CLONING VECTORS FOR THE CONJUGAL TRANSFER OF DNA FROM ESCHERICHIA-COLI TO STREPTOMYCES SPP [J].
BIERMAN, M ;
LOGAN, R ;
OBRIEN, K ;
SENO, ET ;
RAO, RN ;
SCHONER, BE .
GENE, 1992, 116 (01) :43-49
[5]   Identification of a sugar flexible glycosyltransferase from Streptomyces olivaceus, the producer of the antitumor polyketide elloramycin [J].
Blanco, G ;
Patallo, EP ;
Braña, AF ;
Trefzer, A ;
Bechthold, A ;
Rohr, J ;
Méndez, C ;
Salas, JA .
CHEMISTRY & BIOLOGY, 2001, 8 (03) :253-263
[6]   NUCLEOTIDE-SEQUENCES AND HETEROLOGOUS EXPRESSION OF TCMG AND TCMP, BIOSYNTHETIC GENES FOR TETRACENOMYCIN-C IN STREPTOMYCES-GLAUCESCENS [J].
DECKER, H ;
MOTAMEDI, H ;
HUTCHINSON, CR .
JOURNAL OF BACTERIOLOGY, 1993, 175 (12) :3876-3886
[7]   IDENTIFICATION OF STREPTOMYCES-OLIVACEUS TU-2353 GENES INVOLVED IN THE PRODUCTION OF THE POLYKETIDE ELLORAMYCIN [J].
DECKER, H ;
ROHR, J ;
MOTAMEDI, H ;
ZAHNER, H ;
HUTCHINSON, CR .
GENE, 1995, 166 (01) :121-126
[8]   A general approach for cloning and characterizing dNDP-glucose dehydratase genes from actinomycetes [J].
Decker, H ;
Gaisser, S ;
Pelzer, S ;
Schneider, P ;
Westrich, L ;
Wohlleben, W ;
Bechthold, A .
FEMS MICROBIOLOGY LETTERS, 1996, 141 (2-3) :195-201
[9]   A COMPREHENSIVE SET OF SEQUENCE-ANALYSIS PROGRAMS FOR THE VAX [J].
DEVEREUX, J ;
HAEBERLI, P ;
SMITHIES, O .
NUCLEIC ACIDS RESEARCH, 1984, 12 (01) :387-395
[10]   METABOLIC PRODUCTS OF MICROORGANISMS .225. ELLORAMYCIN, A NEW ANTHRACYCLINE-LIKE ANTIBIOTIC FROM STREPTOMYCES-OLIVACEUS - ISOLATION, CHARACTERIZATION, STRUCTURE AND BIOLOGICAL PROPERTIES [J].
DRAUTZ, H ;
REUSCHENBACH, P ;
ZAHNER, H ;
ROHR, J ;
ZEECK, A .
JOURNAL OF ANTIBIOTICS, 1985, 38 (10) :1291-1301