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首页> 外文期刊>Applied Microbiology and Biotechnology >Interplay between pathway-specific and global regulation of the fumonisin gene cluster in the rice pathogen Fusarium fujikuroi
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Interplay between pathway-specific and global regulation of the fumonisin gene cluster in the rice pathogen Fusarium fujikuroi

机译:水稻病原菌Fusarium fujikuroi中伏马菌素基因簇的途径特异性和全局调控之间的相互作用

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摘要

The rice pathogenic fungus Fusarium fujikuroi is known to produce a large variety of secondary metabolites. Besides the gibberellins, causing the bakanae effect in infected rice seedlings, the fungus produces several mycotoxins and pigments. Among the 47 putative secondary metabolite gene clusters identified in the genome of F. fujikuroi, the fumonisin gene cluster (FUM) shows very high homology to the FUM cluster of the main fumonisin producer Fusarium verticillioides, a pathogen of maize. Despite the high level of cluster gene conservation, total fumonisin FB1 and FB2 levels (FBx) produced by F. fujikuroi were only 1-10 % compared to F. verticillioides under inducing conditions. Nitrogen repression was found to be relevant for wild-type strains of both species. However, addition of germinated maize kernels activated the FBx production only in F. verticillioides, reflecting the different host specificity of both wild-type strains. Over-expression of the pathway-specific transcription factor Fum21 in F. fujikuroi strongly activated the FUM cluster genes leading to 1000-fold elevated FBx levels. To gain further insights into the nitrogen metabolite repression of FBx biosynthesis, we studied the impact of the global nitrogen regulators AreA and AreB and demonstrated that both GATA-type transcription factors are essential for full activation of the FUM gene cluster. Loss of one of them obstructs the pathway-specific transcription factor Fum21 to fully activate expression of FUM cluster genes.
机译:水稻致病性真菌镰刀镰刀菌可产生多种次生代谢产物。除了赤霉素,在受感染的水稻幼苗中引起巴卡那菌作用,该真菌还产生多种霉菌毒素和色素。在藤本镰刀菌基因组中鉴定出的47个假定的次级代谢产物基因簇中,伏马菌素基因簇(FUM)与主要伏马菌素生产商Fusarium v​​erticillioides(一种玉米病原体)的FUM簇具有很高的同源性。尽管簇基因的保守程度很高,但在诱导条件下,富士果球菌产生的伏马菌素FB1和FB2的总水平(FBx)仅为褐葡萄球菌的1-10%。发现氮抑制与两个物种的野生型菌株有关。但是,添加发芽的玉米籽粒仅在褐藻中激活了FBx的产生,反映了两种野生型菌株的宿主特异性不同。富士狂犬病菌中途径特异性转录因子Fum21的过度表达强烈激活了FUM簇基因,导致FBx水平提高了1000倍。为了进一步了解FBx生物合成的氮代谢物阻遏作用,我们研究了全局氮调节剂AreA和AreB的影响,并证明了两种GATA型转录因子对于FUM基因簇的完全激活都是必不可少的。其中之一的丢失阻碍了通路特异性转录因子Fum21完全激活FUM簇基因的表达。

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