首页> 外文期刊>Bioscience, Biotechnology, and Biochemistry >Search for transcription factors affecting productivity of the polyketide FR901512 in filamentous fungal sp. No. 14919 and identification of Drf1, a novel negative regulator of the biosynthetic gene cluster
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Search for transcription factors affecting productivity of the polyketide FR901512 in filamentous fungal sp. No. 14919 and identification of Drf1, a novel negative regulator of the biosynthetic gene cluster

机译:搜索影响聚酮化合物FR901512在丝状真菌SP中的生产率的转录因子。 No.14919和DRF1的鉴定,生物合成基因簇的新型负调节剂

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摘要

In order to increase secondary metabolite production in filamentous fungi, a transcription factor gene in the biosynthetic gene cluster and global regulator genes such as laeA are considered plausible as targets for overexpression by genetic modification. In this study, we examined these overexpression effect in fungal sp. No. 14919 that produces FR901512, an HMG-CoA reductase inhibitor. Resultantly, the productivity was improved at 1.7-1.8 fold by overexpressing frlE, a transcription factor gene in the biosynthetic gene cluster, whereas productivity did not change by overexpression of laeA and veA. Furthermore, we searched for extra transcription factors affecting the productivity by transcriptome analysis between wild-type strain and highly productive UV mutants. After verifying productivity decrease by overexpression, Drf1, a novel transcription factor encoded by drf1 was identified as the negative regulator. Because each frlE product (FrlE) and Drf1 worked on the same cluster in positive and negative regulatory manners, their network was analyzed.
机译:为了增加丝状真菌中的次级代谢产物生产,生物合酶基因簇和Laea等全局调节剂基因的转录因子基因被认为是通过遗传修饰过表达的靶标。在这项研究中,我们检查了真菌SP中的这些过表达效应。 No.14919产生FR901512,HMG-COA还原酶抑制剂。结果,通过过表达烧结,在生物合成基因簇中的转录因子基因的过表达因子基因,生产率提高了1.7-1.8的生产率。此外,我们搜索了影响野生型菌株和高效紫外突变体之间的转录组分析生产率的额外转录因子。通过过表达验证生产力降低,DRF1,DRF1编码的新型转录因子被鉴定为负调节剂。因为每个烧风产品(FRLE)和DRF1以正面和负面监管方式的同一集群工作,他们的网络分析了。

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