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通过具有多药敏感酿酒酵母筛选系统的新药发现平台和引入全局次级代谢调节剂 laeA 基因,重新发现 MS-347a 作为一种杀菌剂候选物。

Re-discovery of MS-347a as a fungicide candidate through a new drug discovery platform with a multidrug-sensitive Saccharomyces cerevisiae screening system and the introduction of a global secondary metabolism regulator, laeA gene.

机构信息

Graduate School of Infection Control Sciences, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo, Japan.

Ōmura Satoshi Memorial Institute, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo, Japan.

出版信息

Biosci Biotechnol Biochem. 2024 Jun 21;88(7):824-829. doi: 10.1093/bbb/zbae050.

Abstract

We found that the culture broth of fungi showed anti-fungal activity against multidrug-sensitive budding yeast. However, we could not identify the anti-fungal compound due to the small quantity. Therefore, we attempted to increase the productivity of the target compound by the introduction of a global secondary metabolism regulator, laeA to the strain, which led to the successful isolation of 10-folds greater amount of MS-347a (1) than Aspergillus sp. FKI-5362. Compound 1 was not effective against Candida albicans and the detailed anti-fungal activity of 1 remains unverified. After our anti-fungal activity screening, 1 was found to inhibit the growth of broad plant pathogenic fungal species belonging to the Ascomycota. It is noteworthy that 1 showed little insecticidal activity against silkworms, suggesting its selective biological activity against plant pathogenic fungi. Our study implies that the combination strategy of multidrug-sensitive yeast and the introduction of laeA is useful for new anti-fungal drug discovery.

摘要

我们发现真菌的培养液对多药敏感的出芽酵母具有抗真菌活性。然而,由于数量较少,我们无法鉴定出抗真菌化合物。因此,我们尝试通过向该菌株中引入全局次级代谢调节剂 laeA 来提高目标化合物的产量,这导致成功分离出比 Aspergillus sp. FKI-5362 多 10 倍的 MS-347a(1)。化合物 1 对白色念珠菌无效,其详细的抗真菌活性仍未得到验证。在我们的抗真菌活性筛选后,发现 1 可以抑制属于子囊菌门的广泛植物病原真菌物种的生长。值得注意的是,1 对家蚕的杀虫活性很小,表明其对植物病原真菌具有选择性的生物活性。我们的研究表明,多药敏感酵母与 laeA 引入相结合的策略可用于新型抗真菌药物的发现。

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