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Satoshi Katahira

Researcher at Toyota

Publications -  39
Citations -  1335

Satoshi Katahira is an academic researcher from Toyota. The author has contributed to research in topics: Yeast & Xylose. The author has an hindex of 16, co-authored 38 publications receiving 1233 citations. Previous affiliations of Satoshi Katahira include Kobe University.

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Ethanol fermentation from lignocellulosic hydrolysate by a recombinant xylose- and cellooligosaccharide-assimilating yeast strain

TL;DR: Results demonstrate that the fermentation of the lignocellulose hydrolysate is performed efficiently by the recombinant Saccharomyces strain with abilities for xylose assimilation and cellooligosaccharide degradation.
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Xylose isomerase from polycentric fungus Orpinomyces: gene sequencing, cloning, and expression in Saccharomyces cerevisiae for bioconversion of xylose to ethanol

TL;DR: The cDNA sequence of the gene for xylose isomerase from the rumen fungus Orpinomyces was elucidated by rapid amplification of cDNA ends and revealed that the recombinant enzyme was a homodimer with a subunit of molecular mass 49 kDa.
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Construction of a Xylan-Fermenting Yeast Strain through Codisplay of Xylanolytic Enzymes on the Surface of Xylose-Utilizing Saccharomyces cerevisiae Cells

TL;DR: It is demonstrated that the direct conversion of xylan to ethanol is accomplished by the xylan-utilizing S. cerevisiae strain.
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Improvement of ethanol productivity during xylose and glucose co-fermentation by xylose-assimilating S. cerevisiae via expression of glucose transporter Sut1

TL;DR: Expressing a Pichia stipitis gene encoding a sugar transporter, SUT1, in a xylose-assimilating S. cerevisiae strain increased bothxylose uptake ability and ethanol productivity during xylosedehydrogenase and xylulokinase and glucose uptake ability during glucose fermentation also increased by expressing of Sut1.
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A genome-wide activity assessment of terminator regions in saccharomyces cerevisiae provides a "terminatome" toolbox

TL;DR: The terminator regions of eukaryotes encode functional elements in the 3' untranslated region (3'-UTR) that influence the 3'-end processing of mRNA, mRNA stability, and translational efficiency, which can modulate protein production.