Multiple alternate transcripts direct the biosynthesis of microcystin, a cyanobacterial nonribosomal peptide

被引:111
作者
Kaebernick, M
Dittmann, E
Börner, T
Neilan, BA [1 ]
机构
[1] Univ New S Wales, Sch Microbiol & Immunol, Sydney, NSW 2052, Australia
[2] Humboldt Univ, Inst Biol Genet, Berlin, Germany
关键词
D O I
10.1128/AEM.68.2.449-455.2002
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The mcyABCDEFGHIJ gene cluster of Microcystis aeruginosa encodes the mixed polyketide synthase/nonribosomal peptide synthetase (microcystin synthetase) which is responsible for biosynthesis of the potent liver toxin microcystin. The sequence and orientation of the mcy genes have previously been reported, but no transcriptional analysis had been performed prior to this study. The mcyABCDEFGHIJ genes are transcribed as two polycistronic operons, mcyABC and mcyDEFGHIJ, from a central bidirectional promoter between mcyA and mcyD. Two transcription start sites were detected for both mcyA and mcyD when cells were exposed to light intensities of 68 and 16 mumol of photons m(-2) s(-1). The start sites, located 206 and 254 by upstream of the translational start for mcyD under high and low light conditions, respectively, indicate long untranslated leader regions. Putative transcription start sites were also identified for mcyE, mcyF, mcyG, mcyH, mcyI , and mcyJ but not for mcyB and mcyC. A combination of reverse transcription-PCR and rapid amplification of cDNA ends was employed throughout this work, which may have been one of the first transcriptional analyses of a large nonribosomal polyketide gene cluster.
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页码:449 / 455
页数:7
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