Abstract: The invention relates to mutants and alleles of the coryneform bacterium mqo gene which encodes malate quinone oxidoreductases which contain any amino acid apart from L-serine at position 111, or a comparable position, in the amino acid sequence, and to processes for fermentatively preparing amino acids, preferably L-lysine, L-tryptophan and L-proline, using bacteria which comprise these alleles.
Type:
Grant
Filed:
January 18, 2006
Date of Patent:
May 8, 2007
Assignee:
Degussa AG
Inventors:
Brigitte Bathe, Stephan Hans, Natalie Schischka, Georg Thierbach
Abstract: The present invention relates to a process for the production of L-amino acids by fermentation of recombinant microorganisms of the Enterobacteriaceae family, wherein a) the yfiD ORF and/or the pflB gene or nucleotide sequences coding for the gene products are overexpressed in the microorganisms producing the desired L-amino acid, and the microorganisms are cultured in a medium under conditions in which the desired L-amino acid is enriched in the medium or in the cells; and b) the desired L-amino acid is isolated, in a manner such that constituents of the fermentation broth and/or the biomass in its entirety or in portions (>0 to 100%) either remain in the isolated product or are completely removed.
Abstract: Methods for changing the body temperature of a patient by having them breathe a mist created by nebulizer. The temperature of the mist is adjusted using a heat exchanger. The methods may be used to either cool or warm patients for a variety of clinical reasons. In addition, the invention includes a device (Thermomist) that can be used for generating a mist that can be administered to patients.
Abstract: The invention relates to a process for the production of hydrogen peroxide by the anthraquinone process, comprising a hydrogenation stage, an oxidation stage and an extraction stage. According to the invention, catalytic hydrogenation of anthraquinone derivatives dissolved in a working solution is carried out in the presence of added molecular oxygen. Per mol hydrogen, 0.1 to 10 mmol oxygen is preferably introduced into the hydrogenation stage with the hydrogenating gas, in mixture with an inert gas and/or dissolved and/or dispersed in the working solution. This increases the residence time of the catalyst.
Type:
Grant
Filed:
March 4, 2003
Date of Patent:
March 27, 2007
Assignee:
Degussa AG
Inventors:
Bernd Jaeger, Thomas Haas, Jürgen Glenneberg, Jürgen Grunert
Abstract: The present invention is directed to carbon black granules containing a sorbitan triester. In addition, a process for the production of these carbon black granules is described, in which a powdered carbon black or beaded carbon black is beaded with a sorbitan triester. The carbon black granules can be used in polymer blends, lacquers, inks or pigments.
Abstract: The present invention is directed to DNA elements that enhance cellular gene expression in response to anaerobic growth or the presence of certain inducing agents. The enhancer element may be incorporated into expression vectors and used to increase the production of recombinant proteins.
Type:
Grant
Filed:
January 10, 2002
Date of Patent:
November 23, 2004
Assignee:
The Brigham and Women's Hospital, Inc.
Inventors:
Mark Alan Goldberg, Michael Vasconcelles, Yide Jiang
Abstract: The present invention is directed to a novel neurotensin-like receptor expressed in the central nervous system of humans. The invention encompasses the receptor protein as well as nucleic acids encoding the protein. In addition, the invention is directed to methods and compositions which utilize the receptor.
Type:
Grant
Filed:
July 1, 1999
Date of Patent:
October 5, 2004
Assignee:
AstraZeneca Canada Inc.
Inventors:
Sultan Ahmad, Jack Cao, Dajan O'Donnell, Philippe Walker
Abstract: The present invention is directed to a procedure for making an enantiomerically enriched compound containing a hydronaphthalene ring structure. The process involves reacting oxabenzonorbornadienes with nucleophiles using rhodium as a catalyst and in the presence of a phosphine ligand. The compounds synthesized may be used in pharmaceutical preparations for the treatment of a variety of diseases and conditions.
Abstract: The present invention is directed to a compound of general formula (I),
wherein R1 is selected from phenyl, pyridinyl, thiophenyl, furanyl, imidazolyl; each phenyl ring and heteroaromatic ring optionally and independently being further substituted by 1, 2 or 3 substituents selected from straight and branched C1-C6 alkyl, NO2, CF3, C1-C6 alkoxy, chloro, fluoro, bromo, and iodo, as well as their pharmaceutically acceptable salts. The invention includes pharmaceutical compositions comprising these compounds and the use of the compounds in therapy, in particular in the management of pain.
Type:
Grant
Filed:
October 21, 2002
Date of Patent:
August 31, 2004
Assignee:
AstraZeneca AB
Inventors:
William Brown, Christopher Walpole, Niklas Plobeck
Abstract: Compounds of general formula I
are disclosed and claimed in the present application, as well as their pharmaceutically acceptable salts, pharmaceutical compositions comprising the novel compounds and their use in therapy, in particular in the management of pain.
Type:
Grant
Filed:
June 1, 2000
Date of Patent:
August 17, 2004
Assignee:
AstraZeneca Canada Inc.
Inventors:
Daniel Delorme, Vlad Gregor, Edward Roberts, Eric Sun
Abstract: The present invention relates to certain spirooxindole derivatives and to pharmaceutically acceptable salts thereof, which exhibit good analgesic properties and are effective in the treatment of chronic pain. The derivatives have the structure of formula I:
wherein:
Ar is benzene or pyridine;
X is NHCO—; —CONH—; or —NH—SO2—;
Y is a single bond; and
Z is —CH═CHCH2.
Abstract: Compounds of general formula I
R1 is selected from any one of phenyl, pyridinyl, thienyl, furanyl, imidazolyl, triazolyl and thiazolyl;
where each R1 phenyl ring and R1 heteroaromatic ring may optionally and independently be further substituted by 1, 2 or 3 substituents selected from straight and branched C1-C6 alkyl, NO2, CF3, C1-C6 alkoxy, chloro, fluoro, bromo, and iodo. The substitutions on the phenyl ring and on the heteroaromatic ring may take place in any position on said ring systems;
are disclosed and claimed in the present application, as well as salts and pharmaceutical compositions comprising the novel compounds and their use in therapy, in particular in the management of pain.
Type:
Grant
Filed:
January 16, 2003
Date of Patent:
June 29, 2004
Assignee:
AstraZeneca AB
Inventors:
William Brown, Christopher Walpole, Zhongyong Wei
Abstract: Compounds of general formula I
R1 is selected from any one of phenyl, pyridinyl, thienyl, furanyl, imidazolyl, and triazolyl;
where each R1 phenyl ring and R1 heteroaromatic ring may optionally and independently be further substituted by 1, 2 or 3 substituents selected from straight and branched C1-C6 alkyl, NO2, CF3, C1-C6 alkoxy, chloro, fluoro, bromo, and iodo. The substitutions on the phenyl ring and on the heteroaromatic ring may take place in any position on said ring systems;
are disclosed and claimed in the present application, as well as their pharmaceutically acceptable salts and pharmaceutical compositions comprising the novel compounds and their use in therapy, in particular in the management of pain.
Type:
Grant
Filed:
January 21, 2003
Date of Patent:
June 22, 2004
Assignee:
AstraZeneca AB
Inventors:
William Brown, Christopher Walpole, Zhongyong Wei
Abstract: The present invention is directed to a method for purifying polysaccharides capable of inducing the production of high titers of opsonic antibodies that kill strains of enterococcal bacteria. In addition, the invention is directed to the antigens produced by this purification method and to vaccines which utilize such antigens.
Type:
Grant
Filed:
March 11, 2002
Date of Patent:
April 20, 2004
Assignee:
The Brigham and Women's Hospital, Inc.
Inventors:
Gerald B. Pier, Johannes Huebner, Ying Wang, Lawrence Madoff
Abstract: The present invention is directed to methods of treating a wide variety of diseases, disorders and conditions characterized by excessive activity of substance P. The treatment involves administering peptidases that recognize and selectively cleave polypeptides at Xaa-Pro sequences.
Type:
Grant
Filed:
July 3, 2001
Date of Patent:
March 23, 2004
Assignee:
B.M.R.A. Corporation B.V.
Inventors:
Eric Grouzmann, Jean-Silvain Lacroix, Michel Monod
Abstract: The present invention is directed to therapeutic methods that are based upon an ability to modulate cellular contraction. This is accomplished by administering agents that either inhibit or induce the activity of alpha-smooth muscle actin.
Abstract: Compounds of general formula (I)
wherein m is 0 or 1, and n is 1 or 2;
are disclosed and claimed in the present application, as well as their pharmaceutically acceptable salts, pharmaceutical compositions comprising the novel compounds and their use in therapy, in particular in the management of pain.
Abstract: Compounds of the formula I
are disclosed and claimed in the present application, as well as their pharmaceutically acceptable salts, pharmaceutical compositions comprising the novel compounds and their use in therapy, particular in the management of pain, and more particularly in the management of pain during labor.
Abstract: The present invention is directed to an apparatus that can be used for co-culturing bacteria and eukaryotic cells. The apparatus allows the bacteria to be grown under steady state conditions and then perfused over the eukaryotic cells. The invention also includes a variety of methods for studying the attachment and invasion of host eukaryotic cells by bacteria.
Abstract: The present invention is directed to novel G protein-coupled receptors that are found predominantly in the dorsal root ganglia. The invention encompasses both the receptor proteins as well as nucleic acids encoding the proteins. In addition, the present invention is directed to methods and compositions which utilize the receptors.