Biosynthesis of the polyene antifungal antibiotic nystatin in Streptomyces noursei ATCC 11455:: analysis of the gene cluster and deduction of the biosynthetic pathway

被引:227
作者
Brautaset, T
Sekurova, ON
Sletta, H
Ellingsen, TE
Strom, AR
Valla, S
Zotchev, SB [1 ]
机构
[1] Norwegian Univ Sci & Technol, UNIGEN Ctr Mol BIol, N-7489 Trondheim, Norway
[2] Norwegian Univ Sci & Technol, Dept Biotechnol, N-7489 Trondheim, Norway
[3] SINTEF, SINTEF Appl Chem, N-7034 Trondheim, Norway
来源
CHEMISTRY & BIOLOGY | 2000年 / 7卷 / 06期
关键词
gene cluster; polyene antibiotic; polyketide synthase;
D O I
10.1016/S1074-5521(00)00120-4
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
Background: The polyene macrolide antibiotic nystatin produced by Streptomyces noursei ATCC 11455 is an important antifungal agent. The nystatin molecule contains a polyketide moiety represented by a 38-membered macrolactone ring to which the deoxysugar mycosamine is attached. Molecular cloning and characterization of the genes governing the nystatin biosynthesis is of considerable interest because this information can be used for the generation of new antifungal antibiotics. Results: A DNA region of 1 23,580 base pairs from the S. noursei ATCC 11 455 genome was isolated, sequenced and shown by gene disruption to be involved in nystatin biosynthesis. Analysis of the DNA sequence resulted in identification of six genes encoding a modular polyketide synthase (PKS), genes for thioesterase, deoxysugar biosynthesis, modification, transport and regulatory proteins. One of the PKS-encoding genes, nysC, was found to encode the largest (11,096 amino acids long) modular PKS described to date. Analysis of the deduced gene products allowed us to propose a model for the nystatin biosynthetic pathway in S. noursei. Conclusions: A complete set of genes responsible for the biosynthesis of the antifungal polyene antibiotic nystatin in S. noursei ATCC 11455 has been cloned and analyzed. This represents the first example of the complete DNA sequence analysis of a polyene antibiotic biosynthetic gene cluster. Manipulation of the genes identified within the cluster may potentially lead to the generation of novel polyketides and yield improvements in the production strains.
引用
收藏
页码:395 / 403
页数:9
相关论文
共 38 条
[1]  
AbuSalah KM, 1996, BRIT J BIOMED SCI, V53, P122
[2]  
[Anonymous], 1984, MACROLIDE ANTIBIOTIC
[3]   Organization of the biosynthetic gene cluster for rapamycin in Streptomyces hygroscopicus: Analysis of the enzymatic domains in the modular polyketide synthase [J].
Aparicio, JF ;
Molnar, I ;
Schwecke, T ;
Konig, A ;
Haydock, SF ;
Khaw, LE ;
Staunton, J ;
Leadlay, PF .
GENE, 1996, 169 (01) :9-16
[4]   The biosynthetic gene cluster for the 26-membered ring polyene macrolide pimaricin -: A New polyketide synthase organization encoded by two subclusters separated by functionalization genes [J].
Aparicio, JF ;
Colina, AJ ;
Ceballos, E ;
Martín, JF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (15) :10133-10139
[5]   A chain initiation factor common to both modular and aromatic polyketide synthases [J].
Bisang, C ;
Long, PF ;
Cortés, J ;
Westcott, J ;
Crosby, J ;
Matharu, AL ;
Cox, RJ ;
Simpson, TJ ;
Staunton, J ;
Leadlay, PF .
NATURE, 1999, 401 (6752) :502-505
[7]   Impact of thioesterase activity on tylosin biosynthesis in Streptomyces fradiae [J].
Butler, AR ;
Bate, N ;
Cundliffe, E .
CHEMISTRY & BIOLOGY, 1999, 6 (05) :287-292
[8]   COMPARATIVE-ANALYSIS OF HEXAENE ANTIBIOTICS [J].
CIFTCI, T ;
BORKMAN, TA ;
MCDANIEL, LE ;
SCHAFFNER, CP .
JOURNAL OF ANTIBIOTICS, 1984, 37 (08) :876-884
[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]   MODULAR ORGANIZATION OF GENES REQUIRED FOR COMPLEX POLYKETIDE BIOSYNTHESIS [J].
DONADIO, S ;
STAVER, MJ ;
MCALPINE, JB ;
SWANSON, SJ ;
KATZ, L .
SCIENCE, 1991, 252 (5006) :675-679