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首页> 外文期刊>Fungal Genetics and Biology >Expression of genes encoding laccase and manganese-dependent peroxidase in the fungus Ceriporiopsis subvermispora is mediated by an ACE1-like copper-fist transcription factor
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Expression of genes encoding laccase and manganese-dependent peroxidase in the fungus Ceriporiopsis subvermispora is mediated by an ACE1-like copper-fist transcription factor

机译:编码漆酶和锰依赖性过氧化物酶的基因在真菌小孢子菌中的表达是由ACE1样铜拳转录因子介导的

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摘要

The effect of copper on the expression of genes encoding the ligninolytic enzymes laccase (lcs) and manganese peroxidase (mnp) in Ceriporiopsis subvermispora was evaluated. This metal increased transcript levels of lcs, mnp1 and mnp2. This finding was not unexpected in the case of lcs, since its promoter contains a putative ACE element. Originally characterized in the yeast Saccharomyces cerevisiae, ACE is the target sequence of the ACE1 copper-responsive transcription factor in this microorganism. Analysis of the promoter regions of mnp genes revealed the presence of formerly unnoticed ACE elements. Based on the ace1 gene from Phanerochaete chrysosporium, we isolated and characterized an ACE1-like transcription factor from C. subvermispora (Cs-ACE1) through complementation of a S. cerevisiae ace1Delta strain. Surprisingly, ACE1 factors from both basidiomycetes exhibit substantial differences, not only structurally but also in their ability to complement the aforementioned yeast strain. Specific binding of Cs-ACE1 to its cognate DNA sequence was confirmed by electrophoretic mobility-shift assays.
机译:评估了铜对拟南芥中木质素分解酶漆酶(lcs)和锰过氧化物酶(mnp)编码基因表达的影响。这种金属增加了lcs,mnp1和mnp2的转录水平。对于lcs,这一发现并不令人意外,因为其启动子含有推定的ACE元件。 ACE最初是在啤酒酵母中表征的,是该微生物中ACE1铜响应转录因子的靶序列。对mnp基因启动子区域的分析揭示了以前未被发现的ACE元件的存在。基于来自Phanerochaete chrysosporium的ace1基因,我们通过酿酒酵母ace1Delta菌株的互补分离并鉴定了来自C. subvermispora(Cs-ACE1)的ACE1样转录因子。出人意料的是,来自两种担子菌的ACE1因子不仅在结构上而且在补充上述酵母菌株的能力上均表现出显着差异。 Cs-ACE1与其同源DNA序列的特异性结合已通过电泳迁移率变动分析得以证实。

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