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

Author:

Honma Sota12,Kimishima Aoi12,Kimishima Atsushi3,Honsho Masako12,Kojima Hiroki12,Tokiwa Toshiyuki12,Nishitomi Atsuka1,Kato Satoshi1,Kondo Naozumi1,Araki Yasuko4,Takahashi Tadashi4,Chinen Takumi5,Usui Takeo6ORCID,Fuji Shin-ichi7,Ito Kotaro4,Asami Yukihiro12ORCID

Affiliation:

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

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

3. Graduate School of Pharmaceutical Sciences, Osaka University , 1-6 Yamada-oka, Suita, Osaka , Japan

4. Research and Development Division , Kikkoman Corporation, 338 Noda, Noda-shii, Chiba , Japan

5. Department of Physiological Chemistry, Graduate School of Pharmaceutical Sciences, The University of Tokyo , 7-3-1 Hongo, Bunkyo-ku, Tokyo , Japan

6. Graduate School of Life and Environmental Sciences, University of Tsukuba , 1-1-1 Tennodai, Tsukuba, Ibaraki , Japan

7. Faculty of Bioresource Sciences, Akita Prefectural University , 241-438 Kaidobata-Nishi, Nakano, Shimoshinjo, Akita , Japan

Abstract

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.

Funder

BINDS

Japan Agency for Medical Research and Development

Publisher

Oxford University Press (OUP)

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