Light and the transcriptional response of the microcystin biosynthesis gene cluster

被引:302
作者
Kaebernick, M
Neilan, BA [1 ]
Börner, T
Dittmann, E
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.66.8.3387-3392.2000
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
Microcystin, a hepatotoxin known to be the cause of animal and human deaths, is produced by the bloom-forming cyanobacterium Microcystis aeruginosa in freshwater bodies worldwide. The toxin is produced nonribosomally via a multifunctional enzyme complex, consisting of both peptide synthetase and polyketide synthase modules coded for by the mcy gene cluster. The recent identification of the mcy genes in the production of microcystin synthetase for the first time provides an avenue to study the regulation of microcystin production at a genetic level. In this study, nl. aeruginosa PCC7806 was grown either under continuous light of various intensities or under low light with subsequent short-term exposure to different light intensities and qualities and various stress factors. RNase protection assays were employed to observe the level of mcyB and mcyD transcription under each condition. Both mcyB and mcyD transcript levels were increased under high light intensities and red light. Blue light and certain artificial stress factors (methylviologen and NaCl) led to reduced transcript amounts. There appeared to be two light thresholds, between dark and low light (16 mu mol of photons m(-2) s(-1)), and medium (31 mu mol of photons m(-2) s(-1)) and high light (68 mu mol of photons m(-2) s(-1)), at which a significant increase in transcription occurred. Our findings show that the effect of light on microcystin synthetase production is due to light quality and is initiated lit certain threshold intensities, which are not necessarily reflected by observed intracellular toxin bioactivity.
引用
收藏
页码:3387 / 3392
页数:6
相关论文
共 45 条
[1]   USE OF A COLORIMETRIC PROTEIN PHOSPHATASE INHIBITION ASSAY AND ENZYME-LINKED-IMMUNOSORBENT-ASSAY FOR THE STUDY OF MICROCYSTINS AND NODULARINS [J].
AN, JS ;
CARMICHAEL, WW .
TOXICON, 1994, 32 (12) :1495-1507
[2]  
ANNADOTTER H, 1991, EKOLOGISK STUDIE BLA
[3]  
[Anonymous], P C PRIM PROD MEAS M
[4]   Evidence that microcystin is a thio-template product [J].
Arment, AR ;
Carmichael, WW .
JOURNAL OF PHYCOLOGY, 1996, 32 (04) :591-597
[5]  
BERG K, 1987, ARCH HYDROBIOL, V108, P549
[6]   TOXINS OF CYANOBACTERIA [J].
CARMICHAEL, WW .
SCIENTIFIC AMERICAN, 1994, 270 (01) :78-86
[7]  
Codd GA, 1988, BIOCH ALGAE CYANOBAC
[8]   Insertional mutagenesis of a peptide synthetase gene that is responsible for hepatotoxin production in the cyanobacterium Microcystis aeruginosa PCC 7806 [J].
Dittmann, E ;
Neilan, BA ;
Erhard, M ;
vonDohren, H ;
Borner, T .
MOLECULAR MICROBIOLOGY, 1997, 26 (04) :779-787
[9]   Cell-cell communication in gram-positive bacteria [J].
Dunny, GM ;
Leonard, BAB .
ANNUAL REVIEW OF MICROBIOLOGY, 1997, 51 :527-564
[10]   RAPID MICROFILAMENT REORGANIZATION INDUCED IN ISOLATED RAT HEPATOCYTES BY MICROCYSTIN-LR, A CYCLIC PEPTIDE TOXIN [J].
ERIKSSON, JE ;
PAATERO, GIL ;
MERILUOTO, JAO ;
CODD, GA ;
KASS, GEN ;
NICOTERA, P ;
ORRENIUS, S .
EXPERIMENTAL CELL RESEARCH, 1989, 185 (01) :86-100