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Conserved and essential transcription factors for cellulase gene expression in ascomycete fungi

机译:子囊真菌中纤维素酶基因表达的保守和必需转录因子

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摘要

Rational engineering of filamentous fungi for improved cellulase production is hampered by our incomplete knowledge of transcriptional regulatory networks. We therefore used the model filamentous fungus Neurospora crassa to search for uncharacterized transcription factors associated with cellulose deconstruction. A screen of a N. crassa transcription factor deletion collection identified two uncharacterized zinc binuclear cluster transcription factors (clr-1 and clr-2) that were required for growth and enzymatic activity on cellulose, but were not required for growth or hemicellulase activity on xylan. Transcriptional profiling with next-generation sequencing methods refined our understanding of the N. crassa transcriptional response to cellulose and demonstrated that clr-1 and clr-2 were required for the bulk of that response, including induction of all major cellulase and some major hemicellulase genes. Functional CLR-1 was necessary for expression of clr-2 and efficient cellobiose utilization. Phylogenetic analyses showed that CLR-1 and CLR-2 are conserved in the genomes of most filamentous ascomycete fungi capable of degrading cellulose. In Aspergillus nidulans, a strain carrying a deletion of the clr-2 homolog (clrB) failed to induce cellulase gene expression and lacked cellulolytic activity on Avicel. Further manipulation of this control system in industrial production strains may significantly improve yields of cellulases for cellulosic biofuel production.
机译:我们对转录调节网络的不完全了解阻碍了丝状真菌对纤维素酶生产的合理工程化。因此,我们使用模型丝状真菌Neurospora crassa来搜索与纤维素解构相关的未表征的转录因子。克雷萨斯猪笼草转录因子缺失集合的筛选确定了两个未表征的锌双核簇转录因子(clr-1和clr-2),它们是纤维素的生长和酶促活性所必需的,而不是木聚糖的生长或半纤维素酶活性所必需的。用下一代测序方法进行的转录谱分析使我们对克雷索猪笼草的转录反应有了更深入的了解,并证明了该反应的大部分都需要clr-1和clr-2,包括诱导所有主要的纤维素酶和一些主要的半纤维素酶基因。 。功能性CLR-1是clr-2表达和纤维二糖有效利用所必需的。系统发育分析表明,CLR-1和CLR-2在大多数能够降解纤维素的丝状子囊真菌的基因组中都是保守的。在构巢曲霉中,携带clr-2同系物(clrB)缺失的菌株不能诱导纤维素酶基因表达并且缺乏对Avicel的纤维素分解活性。在工业生产菌株中对该控制系统的进一步操作可以显着提高用于纤维素生物燃料生产的纤维素酶的产量。

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