Bernal Azahara, Jacob Stefan, Andresen Karsten, Yemelin Alexander, Hartmann Holger, Antelo Luis, Thines Eckhard
Institute of Biotechnology and Drug Research gGmbH (IBWF), Hanns-Dieter-Hüsch-Weg 17, D-55128 Mainz, Germany.
Johannes Gutenberg-University Mainz, Microbiology and Biotechnology at the Institute of Molecular Physiology, Hanns-Dieter-Hüsch-Weg 17, D-55128 Mainz, Germany.
Fungal Genet Biol. 2023 Jan;164:103750. doi: 10.1016/j.fgb.2022.103750. Epub 2022 Nov 12.
Microorganisms have been used as biological control agents (BCAs) in agriculture for a long time, but their importance has increased dramatically over the last few years. The Penicillium steckii IBWF104-06 strain has presented strong BCA activity in greenhouse experiments performed against phytopathogenic fungi and oomycetes. P. steckii strains generally produce different antifungal tanzawaic acids; interesting compounds known to be catalyzed by polyketide synthetases in other fungi. Since the decalin structure is characteristic for tanzawaic acids, two polyketide synthase genes (PsPKS1 and PsPKS2) were selected for further analysis, which have similarity in sequence and gene cluster structure with genes that are known to be responsible for the biosynthesis of decalin-containing compounds. Subsequently, gene-inactivation mutants of both PsPKS1 and PsPKS2 have been generated. It was found, that the ΔPspks1 mutant cannot produce tanzawaic acids any more, whereas reintegration of the original PsPKS1 gene into the genome of ΔPspks1 reestablished tanzawaic acid production. The mutant ΔPspks2 is not altered in tanzawaic acids production. Interestingly, both mutants ΔPsPKS1 and ΔPsPKS2 still display strong BCA activity, indicating that the mechanism of action is not related to the production of tanzawaic acids.
长期以来,微生物一直被用作农业中的生物防治剂(BCAs),但在过去几年中其重要性急剧增加。在针对植物病原真菌和卵菌进行的温室实验中,斯氏青霉IBWF104 - 06菌株表现出很强的生物防治活性。斯氏青霉菌株通常会产生不同的抗真菌丹泽酸;这些有趣的化合物在其他真菌中已知是由聚酮合酶催化合成的。由于萘烷结构是丹泽酸的特征,因此选择了两个聚酮合酶基因(PsPKS1和PsPKS2)进行进一步分析,它们在序列和基因簇结构上与已知负责含萘烷化合物生物合成的基因相似。随后,生成了PsPKS1和PsPKS2的基因失活突变体。结果发现,ΔPspks1突变体不再能产生丹泽酸,而将原始的PsPKS1基因重新整合到ΔPspks1的基因组中可恢复丹泽酸的产生。ΔPspks2突变体在丹泽酸产生方面没有变化。有趣的是,ΔPsPKS1和ΔPsPKS2这两个突变体仍然表现出很强的生物防治活性,这表明其作用机制与丹泽酸的产生无关。