Kabushiki Kaisha Toyota Chuo Kenkyusho

Toyota Jidosha Kabushiki Kaisha

Akinori Ikeuchi

Satoshi Katahira

Chie Imamura

Nobuhiko Muramoto

Hiroki Sugimoto

Hidenori Tanaka

Yoichiro Ito

Takashi Matsuyama

Mamoru Yamanishi

Chikara Ohto

Satoshi Kondo

Norihiro Mitsukawa

Haruo Takahashi

Ritsuko Yogo

Risa Nakamura

Risa Onoda

Epigenomic states of genome DNA are altered at multiple sites to rapidly change traits by providing a fusion protein including a first region that defines a polypeptide capable of binding sequence-specifically to multiple sites on genome DNA and a second region that defines a polypeptide capable of regulating an epigenomic state.

Fusion protein for controlling epigenomic state, and use thereof

A method of inducing genetic recombination, including: allowing a protein having DNA double-stranded cleavage activity to act in cells of a eukaryotic organism which is a polyploidy inherently possessed by a eukaryotic organism. In eukaryotic organisms, various genetic recombination generates new genome set composition. This is done to obtain a population of eukaryotic organisms that hold the modified genomic set.

Method of inducing genetic recombination, and use therefor

A method for producing an expression product of an exogenous gene in a yeast, including using at least one yeast gene terminator regions selected based on expression intensity data related to the expression intensity of yeast gene terminator regions to cause expression of a gene in a yeast.

Method for producing expression product of exogenous gene in yeast, regulator of expression in yeast, and use thereof

Provided is a method for producing an expression product of an exogenous gene in a yeast with superior output regulation of gene expression. This is a method for producing an expression product of an exogenous gene in a yeast, including using one or two or more kinds of yeast gene terminator regions selected based on expression intensity data related to the expression intensity of yeast gene terminator regions to cause expression of a gene in a yeast.

A cellobiohydrolase that can contribute to a synergistic effect on cellulose degradation and the use of such cellobiohydrolase in cellulose degradation are provided. The synergistic effect is achieved by an enzyme preparation for cellulose degradation containing a cellobiohydrolase originating inand belonging to GHF6 or a variant thereof, and an endoglucanase originating in a different source other than

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Growing community of inventors

Nagoya, Japan

Akinori Ikeuchi