Mycoscience
Online ISSN : 1618-2545
Print ISSN : 1340-3540
Full paper
Purification and characterization of a fibrinolytic protease from Aspergillus oryzae KSK-3
Norifumi Shirasaka, Masao Naitou, Kazuki Okamura, Yasuhisa Fukuta, Takao Terashita, Mizuho Kusuda
著者情報
キーワード: Edible fungi, Fibrin, Koji, Serine protease
ジャーナル フリー

2012 年 53 巻 5 号 p. 354-364

詳細
抄録

An enzyme from Aspergillus oryzae KSK-3, isolated from commercial rice-koji for miso brewing, showed fibrinolytic activity in liquefied rice culture and was analyzed. A culture filtrate of A. oryzae KSK-3 was concentrated by ultrafiltration and subsequently purified to electrophoretic homogeneity by ammonium sulfate precipitation, ion-exchange chromatography, and gel filtration. The molecular weight of the purified enzyme was estimated to be approximately 30 kDa by SDS-PAGE and high-performance liquid chromatography–size exclusion chromatography. Its maximum fibrinolytic activity was observed at pH 6 and 50°C. The purified protease was stable between pH 4 and 9, at temperatures of up to 50°C. The activity of the enzyme was highest with S-2238 and was considerably inhibited by phenylmethylsufonyl fluoride and pefabloc SC. These results indicate that the enzyme is a serine protease. Moreover, the enzyme is edible and exhibited very high productivity (2,960 U urokinase per milliliter of culture broth). Taken together, the findings of this study indicate that the A. oryzae KSK-3 enzyme may be used as a natural agent for oral fibrinolytic therapy and nutraceutical applications.

著者関連情報
© 2012, by The Mycological Society of Japan
前の記事 次の記事
feedback
Top