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Fumihiko Hasegawa

Researcher at Tohoku University

Publications -  15
Citations -  633

Fumihiko Hasegawa is an academic researcher from Tohoku University. The author has contributed to research in topics: Gene & Peptide sequence. The author has an hindex of 7, co-authored 15 publications receiving 564 citations. Previous affiliations of Fumihiko Hasegawa include National Institute of Advanced Industrial Science and Technology.

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Purification and characterization of a biodegradable plastic-degrading enzyme from Aspergillus oryzae.

TL;DR: Determination of the affinities for different chemicals indicated that the most preferred substrate for the enzyme would consist of butyric acid and n-hexanol, and the environment of the catalytic pocket, which is divided into carboxylic acid and alcohol recognition sites, was investigated.
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Impact of Aspergillus oryzae genomics on industrial production of metabolites.

TL;DR: Genes that have been newly discovered through genome research can be used for the production of novel valuable enzymes and chemicals, and are important for designing new industrial processes.
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Transcriptional analysis of genes for energy catabolism and hydrolytic enzymes in the filamentous fungus Aspergillus oryzae using cDNA microarrays and expressed sequence tags.

TL;DR: The wheat-bran culture gave the richest gene expression profile of hydrolytic enzymes and the lowest expression levels of catabolic genes (EMP, TCA) among the three media tested, suggesting that A. oryzae uses both EMP and TCA for glucose metabolism under AC conditions.
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The fungal hydrophobin RolA recruits polyesterase and laterally moves on hydrophobic surfaces.

TL;DR: Results suggest that RolA adsorbed to the hydrophobic surface of PBSA recruits CutL 1, resulting in condensation of CutL1 on the PBSA surface and consequent stimulation ofPBSA hydrolysis.
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Novel hydrophobic surface binding protein, HsbA, produced by Aspergillus oryzae.

TL;DR: Results suggest that when HsbA is adsorbed onto the PBSA surface, it recruits CutL 1, and that when CutL1 is accumulated on the PB SA surface,It stimulates PBSA degradation via the CutL2 polyesterase.