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Promoter analysis and transcription regulation of fus gene cluster responsible for fusaricidin synthesis of Paenibacillus polymyxa SQR-21

机译:fus基因簇的启动子分析和转录调控,负责fusaricidin合成多粘芽孢杆菌SQR-21的合成

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摘要

Fusaricidins produced by Paenibacillus polymyxa are lipopeptide antibiotics with outstanding antifungal activity. In this study, the whole gene cluster responsible for fusaricidin biosynthesis (fusA) was isolated and identified from the cDNA library of one biocontrol agent P. polymyxa SQR-21 (SQR-21). MALDI-TOF MS analysis confirmed that SQR-21 could produce four kinds of fusaricidins: A, B, C, and D. A central promoter that drove the transcription of fusGFEDCBA was revealed by mapping of the fus promoter region by 5′ deletions. The disruption of fusA in SQR-21 led to the abolishment of fusaricidin production and antifungal activity. The direct interaction between a potential regulator, AbrB, and the promoter region of fus gene cluster was confirmed by electrophoretic mobility shift assays. One abrB disruption mutant showed significantly higher antifungal activity compared with the wild type. These results revealed a pathway for the transcriptional regulation of the fus gene cluster in P. polymyxa.
机译:多粘芽孢杆菌产生的镰刀菌素是脂肽抗生素,具有出色的抗真菌活性。在这项研究中,从一种生物防治剂多粘菌多粘菌SQR-21(SQR-21)的cDNA文库中分离并鉴定了负责镰刀菌素生物合成(fusA)的整个基因簇。 MALDI-TOF MS分析证实SQR-21可以产生4种岩藻毒素素:A,B,C和D。通过绘制5'缺失的fus启动子区域,揭示了驱动fusGFEDCBA转录的中央启动子。 SQR-21中fusA的破坏导致镰刀菌素生产和抗真菌活性的废除。潜在的调节剂,AbrB和fus基因簇的启动子区域之间的直接相互作用已通过电泳迁移率变动分析得以证实。与野生型相比,一种abrB破坏突变体显示出明显更高的抗真菌活性。这些结果揭示了在多粘疟原虫中fus基因簇的转录调控的途径。

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