黑曲霉利用阿魏酸需要转录因子FarA和一种新鉴定的Far样蛋白(FarD),该蛋白缺乏典型的Zn(II)2Cys6结构域。

IF 2.1 Q3 MYCOLOGY Frontiers in fungal biology Pub Date : 2022-11-08 eCollection Date: 2022-01-01 DOI:10.3389/ffunb.2022.978845
Mark Arentshorst, Jos Reijngoud, Daan J C van Tol, Ian D Reid, Yvonne Arendsen, Herman J Pel, Noël N M E van Peij, Jaap Visser, Peter J Punt, Adrian Tsang, Arthur F J Ram
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引用次数: 0

摘要

阿魏酰酯酶B基因(faeB)是由羟基肉桂酸(如阿魏酸、咖啡酸和香豆素酸)特异性诱导的,但参与faeB诱导和阿魏酸代谢的转录调控网络仅被部分解决。为了鉴定参与阿魏酸代谢的转录因子,我们构建并筛选了239株黑曲霉的转录因子敲除文库,以寻找不能利用阿魏酸作为碳源的突变体。已知参与脂肪酸代谢的ΔfarA转录因子突变体不能利用阿魏酸和其他羟基肉桂酸。除了筛选转录因子突变体集合外,还进行了正向遗传筛选以分离不能表达faeB的突变体。针对该筛选,设计了PfaeB-aamdS和PfaeB-lux613双报告菌株。筛选的基本原理是,在该报告菌株中,阿魏酸通过faeB启动子诱导amdS(乙酰氨基酶)表达,导致对氟乙酰胺的致死性。将该报告菌株的Conidia进行UV诱变,并在阿魏酸存在下在氟乙酰胺培养基上铺板。不能诱导faeB的突变体预计对氟乙酰胺具有耐药性,并且可以积极选择。使用该筛选,获得了六个氟乙酰胺抗性突变体,并对其进行了表型表征。三个突变体具有与farA突变体相同的表型,并且对这些突变体中的farA基因进行测序确实显示了farA的突变,这导致不能在阿魏酸以及短链和长链脂肪酸上生长。其他三个突变体的生长表型在不能在阿魏酸上生长方面与farA突变体相似,但这些突变体在短链和长链脂肪酸上正常生长。对这三个突变体的基因组进行了测序,并在一个特定基因(NRRL3_09145)中发现了等位基因突变。NRRL3_09145编码的蛋白质与FarA和FarB转录因子具有相似性。然而,尽管FarA和FarB同时包含Zn(II)2Cys6结构域和真菌特异性转录因子结构域,但由NRRL3_09145(FarD)编码的蛋白质缺乏典型的Zn(II,2Cys6)结构域,并且仅具有真菌特异性的转录因子结构区。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Utilization of ferulic acid in Aspergillus niger requires the transcription factor FarA and a newly identified Far-like protein (FarD) that lacks the canonical Zn(II)2Cys6 domain.

The feruloyl esterase B gene (faeB) is specifically induced by hydroxycinnamic acids (e.g. ferulic acid, caffeic acid and coumaric acid) but the transcriptional regulation network involved in faeB induction and ferulic acid metabolism has only been partially addressed. To identify transcription factors involved in ferulic acid metabolism we constructed and screened a transcription factor knockout library of 239 Aspergillus niger strains for mutants unable to utilize ferulic acid as a carbon source. The ΔfarA transcription factor mutant, already known to be involved in fatty acid metabolism, could not utilize ferulic acid and other hydroxycinnamic acids. In addition to screening the transcription factor mutant collection, a forward genetic screen was performed to isolate mutants unable to express faeB. For this screen a PfaeB-amdS and PfaeB-lux613 dual reporter strain was engineered. The rationale of the screen is that in this reporter strain ferulic acid induces amdS (acetamidase) expression via the faeB promoter resulting in lethality on fluoro-acetamide. Conidia of this reporter strain were UV-mutagenized and plated on fluoro-acetamide medium in the presence of ferulic acid. Mutants unable to induce faeB are expected to be fluoro-acetamide resistant and can be positively selected for. Using this screen, six fluoro-acetamide resistant mutants were obtained and phenotypically characterized. Three mutants had a phenotype identical to the farA mutant and sequencing the farA gene in these mutants indeed showed mutations in FarA which resulted in inability to growth on ferulic acid as well as on short and long chain fatty acids. The growth phenotype of the other three mutants was similar to the farA mutants in terms of the inability to grow on ferulic acid, but these mutants grew normally on short and long chain fatty acids. The genomes of these three mutants were sequenced and allelic mutations in one particular gene (NRRL3_09145) were found. The protein encoded by NRRL3_09145 shows similarity to the FarA and FarB transcription factors. However, whereas FarA and FarB contain both the Zn(II)2Cys6 domain and a fungal-specific transcription factor domain, the protein encoded by NRRL3_09145 (FarD) lacks the canonical Zn(II)2Cys6 domain and possesses only the fungal specific transcription factor domain.

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