Abstract: Genetic recombinant yeast expressing xylose reductase (XR), (wild-type or mutant) xylitol dehydrogenase (XDH), and xylulokinase (XK) and a method for highly efficiently producing ethanol from xylose using the yeast are provided. Pichia stipitis-derived XR and (wild-type or modified-type) XDH genes and Saccharomyces cerevisiae-derived XK gene were introduced via chromosomal integration. Thus, a genetic recombinant yeast having a high xylose fermentation rate, being capable of producing ethanol from xylose in high yields, and having high xylose fermentability in the presence of glucose, as well as a method using the recombinant yeast for highly efficiently producing ethanol from xylose or a saccharified solution from lignocellulose-based biomass are provided. Furthermore, a method for improving the xylose fermentability of the genetic recombinant yeast of the present invention via acclimatization treatment is also provided herein.

Abstract: Disclosed is the production of useful substances such as bioethanol from pentose through effective use of biomass resources. Specifically, the invention discloses the following: Use of HGT2 gene or an expression product protein thereof as a xylose transporter. A xylose and/or L-arabinose transporter as an expression product protein of a gene selected from the group consisting of HGT2 gene, XUT1 gene, and HXT2.4 gene. Use of a gene selected from the group consisting of HGT2 gene, XUT1 gene, and HXT2.4 gene as a xylose and/or L-arabinose transporter. A method for producing bioethanol, the method comprising introducing into yeast at least one gene selected from the group consisting of HGT2 gene, XUT1 gene, and HXT2.4 gene, and culturing the yeast in the presence of a biomass that contains xylose and/or L-arabinose.

Abstract: The present invention provides a novel cellulase-producing fungus, i.e. Acremonium cellulolyticus CF-2612 strain or a mutant thereof, which has an ability to produce cellulase so highly, a method for producing cellulase and/or hemicellulase by culturing said fungus, and a method for degrading or saccharifying biomass using the cellulase and/or hemicellulase.

Abstract: Genetic recombinant yeast expressing xylose reductase (XR), (wild-type or mutant) xylitol dehydrogenase (XDH), and xylulokinase (XK) and a method for highly efficiently producing ethanol from xylose using the yeast are provided. Pichia stipitis-derived XR and (wild-type or modified-type) XDH genes and Saccharomyces cerevisiae-derived XK gene were introduced via chromosomal integration. Thus, a genetic recombinant yeast having a high xylose fermentation rate, being capable of producing ethanol from xylose in high yields, and having high xylose fermentability in the presence of glucose, as well as a method using the recombinant yeast for highly efficiently producing ethanol from xylose or a saccharified solution from lignocellulose-based biomass are provided. Furthermore, a method for improving the xylose fermentability of the genetic recombinant yeast of the present invention via acclimatization treatment is also provided herein.

Abstract: The present invention relates to a process for producing ethanol by carrying out the following steps: performing enzymatic saccharification of pre-treated lignocellulosic biomass in a reaction system; performing ethanol fermentation of fermentable sugars obtained from the saccharified pre-treated lignocellulosic biomass in the same reaction zone as the enzymatic saccharification; distilling ethanol directly off from a reaction treatment liquid in the reaction zone, so as to recover the ethanol.

Abstract: The present invention provides a novel cellulase-producing fungus, i.e. Acremonium cellulolyticus CF-2612 strain or a mutant thereof, which has an ability to produce cellulase so highly, a method for producing cellulase and/or hemicellulase by culturing said fungus, and a method for degrading or saccharifying biomass using the cellulase and/or hemicellulase.

Abstract: A process of treating a liquid waste containing organic matters, which includes contacting, in a digestion zone maintained in anaerobic conditions, the liquid waste with bacterial granules of (a) acid fermentation bacteria and/or methane-producing bacteria and (b) phototrophic bacteria, while irradiating the bacterial granules with light, to digest the organic matters and to proliferate the phototrophic bacteria.

Abstract: Garbage resulting from the preparation, cooking and dispensing of food and containing water-insoluble organic components is treated first heated in the presence of water at a temperature of 100.degree.-400.degree. C. and a pressure higher than the saturated water vapor pressure to convert at least part of the water-insoluble components into water-soluble organic components and to obtain a mixture containing the water-soluble components dissolved in the water. The mixture is then subjected to methane fermentation to convert the water-soluble organic components into methane.

Abstract: Water containing an inorganic nitrogen-containing compound, such as water effluent from sewage treatment plant, is treated for the removal of the nitrogen-containing compound and for the production of hydrocarbons by proliferating microalga capable of consuming the nitrogen-containing compound and of producing the hydrocarbons as an intracellular product. After adjusting the water content, the resulting culture containing the proliferated microalga and clean water is heated at a high temperature and a high pressure to liberate the hydrocarbon from the microalga. The hydrocarbon is subsequently recovered by solvent extraction.