A polyketide synthase gene required for biosynthesis of the aflatoxin-like toxin, dothistromin

被引:42
作者
Bradshaw, RE [1 ]
Jin, HP
Morgan, BS
Schwelm, A
Teddy, OR
Young, CA
Zhang, SG
机构
[1] Massey Univ, Inst Mol BioSci, Natl Ctr Adv Bioprotect Technol, Palmerston North, New Zealand
[2] Noble Fdn Inc, Ardmore, OK USA
关键词
aflatoxin biosynthesis; Dothistroma septosporum; dothistromin biosynthesis; epoxide hydrolase; red-band needle blight; sporulation;
D O I
10.1007/s11046-006-0240-5
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Dothistromin is a polyketide toxin, produced by a fungal forest pathogen, with structural similarity to the aflatoxin precursor versicolorin B. Biochemical and genetic studies suggested that there are common steps in the biosynthetic pathways for these metabolites and showed similarities between some of the genes. A polyketide synthase gene (pksA) was isolated from dothistromin-producing Dothistroma septosporum by hybridization with an aflatoxin ortholog from Aspergillus parasiticus. Inactivation of this gene in D. septosporum resulted in mutants that could not produce dothistromin but that could convert exogenous aflatoxin precursors, including norsolorinic acid, into dothistromin. The mutants also had reduced asexual sporulation compared to the wild type. So far four other genes are known to be clustered immediately alongside pksA. Three of these (cypA, moxA, avfA) are predicted to be orthologs of aflatoxin biosynthetic genes. The other gene (epoA), located between avfA and moxA, is predicted to encode an epoxide hydrolase, for which there is no homolog in either the aflatoxin or sterigmatocystin gene clusters. The pksA gene is located on a small chromosome of similar to 1.3 Mb in size, along with the dothistromin ketoreductase (dotA) gene.
引用
收藏
页码:283 / 294
页数:12
相关论文
共 41 条
[1]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[2]  
[Anonymous], SCIENCE
[3]   Cloning and molecular characterization of a soluble epoxide hydrolase from Aspergillus niger that is related to mammalian microsomal epoxide hydrolase [J].
Arand, M ;
Hemmer, H ;
Dürk, H ;
Baratti, J ;
Archelas, A ;
Furstoss, R ;
Oesch, F .
BIOCHEMICAL JOURNAL, 1999, 344 :273-280
[4]  
Barnes I, 2004, STUD MYCOL, P551
[5]   SYNTHESIS OF STERIGMATOCYSTIN ON A CHEMICALLY-DEFINED MEDIUM BY SPECIES OF ASPERGILLUS AND CHAETOMIUM [J].
BARNES, SE ;
DOLA, TP ;
BENNETT, JW ;
BHATNAGAR, D .
MYCOPATHOLOGIA, 1994, 125 (03) :173-178
[6]   Mycotoxins [J].
Bennett, JW ;
Klich, M .
CLINICAL MICROBIOLOGY REVIEWS, 2003, 16 (03) :497-+
[7]   Molecular genetic analysis and regulation of aflatoxin biosynthesis [J].
Bhatnagar, D ;
Ehrlich, KC ;
Cleveland, TE .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2003, 61 (02) :83-93
[8]   Dothistroma (red-band) needle blight of pines and the dothistromin toxin: a review [J].
Bradshaw, RE .
FOREST PATHOLOGY, 2004, 34 (03) :163-185
[9]   High levels of dothistromin toxin produced by the forest pathogen Dothistroma pini [J].
Bradshaw, RE ;
Ganley, RJ ;
Jones, WT ;
Dyer, PS .
MYCOLOGICAL RESEARCH, 2000, 104 :325-332
[10]   Transformation of the fungal forest pathogen Dothistroma pini to hygromycin resistance [J].
Bradshaw, RE ;
Bidlake, A ;
Forester, N ;
Scott, DB .
MYCOLOGICAL RESEARCH, 1997, 101 :1247-1250