scispace - formally typeset
T

Takashi Hirasawa

Researcher at Tokyo Institute of Technology

Publications -  92
Citations -  3665

Takashi Hirasawa is an academic researcher from Tokyo Institute of Technology. The author has contributed to research in topics: Corynebacterium glutamicum & Saccharomyces cerevisiae. The author has an hindex of 30, co-authored 87 publications receiving 3337 citations. Previous affiliations of Takashi Hirasawa include Osaka University & Mitsui Chemicals.

Papers
More filters
Journal ArticleDOI

Comprehensive phenotypic analysis for identification of genes affecting growth under ethanol stress in Saccharomyces cerevisiae.

TL;DR: The growth behavior of all available single gene deletion strains of budding yeast under ethanol stress revealed that the growth of 446 deletion strains under stress induced by 8% ethanol was defective, and the genes and functional categories identified might provide clues to improving ethanol stress tolerance among yeast cells.
Journal ArticleDOI

Identification of target genes conferring ethanol stress tolerance to Saccharomyces cerevisiae based on DNA microarray data analysis.

TL;DR: Results indicate that overexpression of the genes for trypophan biosynthesis increases the ethanol stress tolerance, and Tryptophan supplementation to culture and overexpressive of the tryptophan permease gene are also effective for the increase in ethanol stressolerance.
Journal ArticleDOI

Comprehensive phenotypic analysis of single-gene deletion and overexpression strains of Saccharomyces cerevisiae.

TL;DR: Genome‐wide analyses enabled the extraction of the genes and identification of the functional categories for which genetic perturbation caused the change of growth behaviour, and identified several functional categories having fragility and robustness for cellular growth.
Journal ArticleDOI

Transcriptome analysis of parallel-evolved Escherichia coli strains under ethanol stress

TL;DR: Genes related to iron ion metabolism were commonly up-regulated in the tolerant strains, which suggests the change in intracellular redox state during adaptive evolution.