| Literature DB >> 30821612 |
Hiroya Itoh1,2, Ai Miura3, Itaru Takeda3, Makoto Matsui2,4, Koichi Tamano3, Masayuki Machida2,3, Takashi Shibata2,4.
Abstract
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.Entities:
Keywords: FR091512 polyketide; HMG-CoA reductase inhibitor; fungal sp. No. 14919; secondary metabolism; transcriptional factor
Mesh:
Substances:
Year: 2019 PMID: 30821612 DOI: 10.1080/09168451.2019.1584519
Source DB: PubMed Journal: Biosci Biotechnol Biochem ISSN: 0916-8451 Impact factor: 2.043