Abstract: The present invention includes an inflow quantity regulating means 5 for regulating the inflow quantity of a fuel gas to a compressor 1; a recycle valve 7 for returning the fuel gas discharged from the compressor 1 to the inlet side of the compressor 1; and a control means which sets a control operating value for operating the compressor 1 at a predetermined operation point, and controls the inflow quantity regulating means 5 and the recycle valve 7 based on the control operating value. The control means has a first control signal generating means 27 which generates a signal increasing with an increase in the operating value as a control signal for the inflow quantity regulating means 5 when the control operating value is a predetermined value or larger and a second control signal generating means 29 which generates a signal decreasing with an increase in the operating value as a control signal for the recycle valve 7 when the control operating value is smaller than the predetermined value.

Abstract: Provided is a bacterium which is capable of producing an organic acid and is modified so as to have an enhanced 2-oxoglutarate dehydrogenase activity as compared with that of an unmodified strain. An organic acid such as succinic acid can be produced by culturing the bacterium.

Abstract: Disclosed is a process for production of succinic acid, which comprises the step of reacting a bacterium which has been modified so as to increase the expression of a sucE1 gene or a product produced by any treatment of the bacterium with an organic raw material in a reaction solution containing a carbonate ion, a bicarbonate ion or carbon dioxide gas to thereby yield the desired succinic acid.

Abstract: Coryneform bacterium is modified so that an activity of acetyl-CoA hydrolase is decreased, and succinic acid is produced by using the bacterium.

Abstract: A hand drying apparatus includes a hand inserting portion having a concave shape including a front inner wall facing a back inner wall, an airflow generator that generates high-pressure airflows, and a first air nozzle and a second air nozzle that inject the high-pressure airflows to the hand inserting portion. The first air nozzle is provided on the front inner wall and the second air nozzle is provided on the back inner wall. The first air nozzle includes slip-shaped first holes arranged in a line, each having a first length. The second air nozzle includes slip-shaped second holes arranged in a line, each having a second length. The first length and the second length are different.

Abstract: A feeding mechanism, having a base station to which an elongate base material is continuously fed to be physically or chemically processed at a prescribed speed and from which the processed base material is continuously recovered, wherein tensile force T1 in a direction opposite to a feeding direction is applied at a supply side of the base station, frictional force F is applied at the base station and tensile force T2 in the feeding direction is applied at the recovery side of the base station, on said base material, with these forces satisfying the relation of F>T1>T2, is provided. A feeding mechanism for feeding a base material for performing physical or chemical processing with high accuracy while an elongate base material is continuously fed, particularly a feeding mechanism that suppresses thickness variation along the lengthwise direction or surface damage at a portion where a function is added of the processed base material, can be obtained.

Abstract: L-Glutamic acid is produced by culturing a coryneform bacterium having L-glutamic acid producing ability, in which trehalose synthesis ability is decreased or deleted by, for example, disrupting the otsA gene derived from a coryneform bacterium source, coding for trehalose-6-phosphate synthase, to produce and accumulate L-glutamic acid in the medium, and collecting the L-glutamic acid from the medium.

Abstract: Coryneform bacteria are described that have an ability to produce L-amino acids and are modified so that acetyl-CoA hydrolase activity is decreased. The bacteria are used to produce L-amino acids generated by a biosynthetic pathway in which pyruvic acid is an intermediate, such as L-glutamic acid, L-arginine, L-glutamine, L-proline, L-alanine, L-valine, and L-lysine.

Abstract: L-Glutamine is produced by culturing a coryneform bacterium which has L-glutamine producing ability and has been modified so that its intracellular glutamine synthetase activity should be enhanced, preferably which has been further modified so that its intracellular glutamate dehydrogenase activity should be enhanced, in a medium to produce and accumulate L-glutamine in the medium and collecting the L-glutamine.

Abstract: A printing system configured by connecting, over a network, a printing request instruction terminal for making a printing request including reference information that indicates a storage location of the paper original data, a server which accepts the printing request from the printing request instruction terminal, designates a printer as a printing destination according to the printing request and makes a printing instruction to that printer, and multiple printers which execute printing according to the printing instruction from the server, wherein the server comprises: an examination unit which, when receives the printing request from the printing request instruction terminal, examines whether or not the printer designated as the printing destination has a pull-printing function to execute printing by obtaining the paper original data according to the reference information; and a print control unit which obtains the paper original data according to the reference information when it is found as a result of th

Abstract: A coryneform bacterium which has an L-glutamic acid-producing ability and grows at least at the same growth rate as a non-mutated strain or a wild-type strain and has intracellular ?-ketoglutarate dehydrogenase activity which is less than half that of the non-mutated or wild-type strain, and is obtained by introducing a mutation into a coding region or an expression control region of the chromosomal odhA gene encoding the E1o subunit of the ?-ketoglutarate dehydrogenase complex.

Abstract: Succinic acid is produced by using a coryneform bacterium which has succinic acid-producing ability and has been modified so that an activity of pyruvate oxidase is decreased.

Abstract: L-Glutamine is produced by culturing a coryneform bacterium which has L-glutamine producing ability and has been modified so that its intracellular glutamine synthetase activity should be enhanced, preferably which has been further modified so that its intracellular glutamate dehydrogenase activity should be enhanced, in a medium to produce and accumulate L-glutamine in the medium and collecting the L-glutamine.

Abstract: A coryneform bacterium which has an L-glutamic acid-producing ability and grows at least at the same growth rate as a non-mutated strain or a wild-type strain and has intracellular ?-ketoglutarate dehydrogenase activity which is less than half that of the non-mutated or wild-type strain, and is obtained by introducing a mutation into a coding region or an expression control region of the chromosomal odhA gene encoding the E1o subunit of the ?-ketoglutarate dehydrogenase complex.

Abstract: Succinic acid is produced by allowing a bacterium modified to enhance fumarate reductase activity or cell preparation thereof to react with an organic raw material in a reaction solution containing one of a carbonate ion, a bicarbonate ion, and carbon dioxide gas to generate succinic acid. More preferably, succinic acid is produced by allowing a bacterium modified to enhance activities of fumarate reductase and pyruvate carboxylase and decrease lactate dehydrogenase activity or cell preparation thereof to react with an organic raw material in a reaction solution containing one of a carbonate ion, a bicarbonate ion, and carbon dioxide gas to generate succinic acid. Succinic acid is obtained by collecting the produced succinic acid.

Abstract: A moving image distribution system, wherein the user can view content moving images at no charge, and the provider of the content moving images can prevent a drain of the moving image contents and can protect the copy right thereof, as a copy right holder, without fail. The moving images are divided, along a time axis, into two master and slave nonreproducible moving image files. The slave moving image file (small file) is encrypted based on CM file data in which a predetermined CM element has been incorporated. In response to a reproduction request of a user terminal that possesses the master moving image file (main file) in advance, the slave moving image file is distributed with the CM moving images to the user terminal via a network line such as the Internet.

Abstract: A coryneform bacterium that is modified by using a yggB gene so that L-glutamic acid-producing ability is enhanced as compared to a non-modified strains is cultured in a medium to cause accumulation of L-glutamic acid in the medium or bacterial cells, and L-glutamic acid is collected from the medium or cells.

Abstract: A coryneform bacterium which has an L-glutamic acid-producing ability and grows at least at the same growth rate as a non-mutated strain or a wild-type strain and has intracellular ?-ketoglutarate dehydrogenase activity which is less than half that of the non-mutated or wild-type strain, and is obtained by introducing a mutation into a coding region or an expression control region of the chromosomal odhA gene encoding the E1o subunit of the ?-ketoglutarate dehydrogenase complex.

Abstract: A method of producing coryneform bacteria having an improved amino acid- or nucleic acid-productivity comprises the steps of introducing a mutation in a promoter sequence of amino acid- or nucleic acid-biosynthesizing genes on a chromosome of a coryneform bacterium to make it close to a consensus sequence or introducing a change in a promoter sequence of amino acid- or nucleic acid-biosynthesizing genes on a chromosome of a coryneform bacterium by gene recombination to make it close to a consensus sequence, to obtain mutants of the coryneform amino acid d- or nucleic acid-producing microorganism, culturing the mutants and select a mutant capable of producing the intended amino acid or nucleic acid in a large amount. This method can construct a mutant capable of suitably enriching or controling the expression of an intended gene without using a plasmid and also capable of producing amino acids in a high yield, by the recombination or mutation.

Abstract: A method of producing coryneform bacteria having improved amino acid or nucleic acid productivity comprising the steps of introducing a mutation in a promoter sequence of amino acid- or nucleic acid-biosynthesizing genes on a chromosome of a coryneform bacterium to make it close to a consensus sequence, or introducing a change in a promoter sequence of amino acid- or nucleic acid-biosynthesizing genes on a chromosome of a coryneform bacterium by gene recombination to make it close to a consensus sequence, to obtain mutants of the coryneform amino acid- or nucleic acid-producing microorganism, culturing the mutants and selecting a mutant capable of producing the intended amino acid or nucleic acid in a large amount. This method allows the construction of a mutant capable of enriching or controlling the expression of an intended gene without using a plasmid and to promote production of amino acids in a high yield by recombination or mutation.