An optical micro-ring modulator (MRM) requires temperature tracking and locking such that the resonance notches/peaks of the MRM device are actively thermally shifted to coincide with the narrow input optical wavelength. Accordingly, it would be beneficial to auto tune an MRM device so that it functions as a high-speed modulator and accommodates initial process variations in manufacturing, the random thermal heating and cooling of the environment, and drift of the input laser line wavelength. The control system generates an error signal by comparing complementary tapped optical signals from the through and drop output waveguides of the MRM device where the controller is tuned to the high-speed electrical modulation of the device along with the slow-speed thermal transient behaviour of the MRM device. The controller can operate using balanced electrical modulation code, non-balanced modulation code and tuned to optimize for optical amplitude modulation (OMA) and extinction ratio.
H03L 7/085 - Détails de la boucle verrouillée en phase concernant principalement l'agencement de détection de phase ou de fréquence, y compris le filtrage ou l'amplification de son signal de sortie
G02B 6/12 - Guides de lumièreDétails de structure de dispositions comprenant des guides de lumière et d'autres éléments optiques, p. ex. des moyens de couplage du type guide d'ondes optiques du genre à circuit intégré
H01S 3/08 - Structure ou forme des résonateurs optiques ou de leurs composants
2.
APTAMER-BASED ELECTROCHEMICAL DRUG DETECTION ASSAY
Aptamers configured to specifically bind to tetrahydrocannabinol and cannabidiol are disclosed, and biosensing methods and biosensor devices are described in which such aptamers are employed for detection of tetrahydrocannabinol and/or cannabidiol, with a limit of detection in the nanomolar range. In some example implementations, aptamer-based electrochemical biosensors are disclosed for sensitive and rapid detection of tetrahydrocannabinol and/or cannabidiol. Examples of microfluidic biosensors are disclosed that may be utilized in point-of-care settings.
G01N 33/543 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet avec un support insoluble pour l'immobilisation de composés immunochimiques
C12N 15/115 - Aptamères, c.-à-d. acides nucléiques liant spécifiquement une molécule cible avec une haute affinité sans s'y hybrider
G01N 33/53 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet
G01N 33/94 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des narcotiques
THE ROYAL INSTITUTION FOR THE ADVANCEMENT OF LEARNING/MCGILL UNIVERSITY (Canada)
CONCORDIA UNIVERSITY (Canada)
Inventeur(s)
Larose, Joel
Moreau, Christian
Stoyanov, Pantcho P.
Sharifi, Navid
Chromik, Richard
Makowiec, Mary E.
Patel, Payank
Abrégé
A seal has: a metallic substrate; and a coating layer, The coating layer has in atomic percent of all metals in the coating layer: 6.5 to 22.0 Al; 14.0 to 23.0 Fe; 14.0 to 23.0 Co; 14.0 to 23.0 Cr; 14.0 to 23.0 Mn; and 14.0 to 23.0 Ni. The coating may be applied by high velocity oxy-fuel (HVOF) spray.
C23C 28/00 - Revêtement pour obtenir au moins deux couches superposées, soit par des procédés non prévus dans un seul des groupes principaux , soit par des combinaisons de procédés prévus dans les sous-classes et
C23C 30/00 - Revêtement avec des matériaux métalliques, caractérisé uniquement par la composition du matériau métallique, c.-à-d. non caractérisé par le procédé de revêtement
F02C 7/28 - Agencement des dispositifs d'étanchéité
F02F 5/00 - Segments de piston, p. ex. associés avec la tête de piston
F02F 11/00 - Aménagements des garnitures d'étanchéité dans les moteurs à combustion
4.
COCR ALLOY CARBIDE COMPOSITE COATINGS FOR HIGH-TEMPERATURE APPLICATIONS
THE ROYAL INSTITUTION FOR THE ADVANCEMENT OF LEARNING/MCGILL UNIVERSITY (Canada)
CONCORDIA UNIVERSITY (Canada)
Inventeur(s)
Larose, Joel
Moreau, Christian
Stoyanov, Pantcho P.
Sharifi, Navid
Chromik, Richard
Makowiec, Mary E.
Encalada, Alejandra Islas
Abrégé
A method for applying a coating, includes: providing a mixture of powders of comprising by volume percent: 10.0 to 60.0 one or more cobalt-based alloys and 5.0 to 70.0 WC-Ni; and spraying the mixture on a metallic substrate. Each of the cobalt-based alloys have by weight percent: Co as a largest constituent; 20.0-35.0 Cr; up to 3.0 C, if any; and up to 4.0 Ni, if any.
C23C 30/00 - Revêtement avec des matériaux métalliques, caractérisé uniquement par la composition du matériau métallique, c.-à-d. non caractérisé par le procédé de revêtement
F02C 7/28 - Agencement des dispositifs d'étanchéité
F02F 5/00 - Segments de piston, p. ex. associés avec la tête de piston
F02F 11/00 - Aménagements des garnitures d'étanchéité dans les moteurs à combustion
The Royal Institution for the Advancement of Learning/McGill University (Canada)
Inventeur(s)
Patel, Payank
Makowiec, Mary E.
Larose, Joël
Sharifi, Navid
Stoyanov, Pantcho P.
Moreau, Christian
Chromik, Richard
Abrégé
A seal has: a metallic substrate; and a coating layer, The coating layer has in atomic percent of all metals in the coating layer: 6.5 to 22.0 Al; 14.0 to 23.0 Fe; 14.0 to 23.0 Co; 14.0 to 23.0 Cr; 14.0 to 23.0 Mn; and 14.0 to 23.0 Ni. The coating may be applied by high velocity oxy-fuel (HVOF) spray.
C23C 4/073 - Matériaux métalliques contenant des alliages MCrAl ou MCrAlY où M est le nickel, le cobalt ou le fer, avec ou sans éléments non métalliques
C22C 30/00 - Alliages contenant moins de 50% en poids de chaque constituant
The Royal Institution for the Advancement of Learning/McGill University (Canada)
Inventeur(s)
Islas Encalada, Alejandra
Larose, Joël
Makowiec, Mary E.
Stoyanov, Pantcho P.
Moreau, Christian
Sharifi, Navid
Chromik, Richard
Abrégé
A method for applying a coating, includes: providing a mixture of powders of comprising by volume percent: 10.0 to 60.0 one or more cobalt-based alloys and 5.0 to 70.0 WC—Ni; and spraying the mixture on a metallic substrate. Each of the cobalt-based alloys have by weight percent: Co as a largest constituent; 20.0-35.0 Cr; up to 3.0 C, if any; and up to 4.0 Ni, if any.
The Royal Institution for the Advancement of Learning/McGill University (Canada)
Inventeur(s)
Patel, Payank
Makowiec, Mary E.
Larose, Joël
Sharifi, Navid
Stoyanov, Pantcho P.
Moreau, Christian
Chromik, Richard
Abrégé
A method for repairing damage at a damage site on the surface of a nickel- or cobalt-based alloy. The method includes: machining at the damage site; and applying a high entropy alloy (HEA) repair material to the damage site via high velocity oxy-fuel (HVOF) spray, high velocity air-fuel (HVAF) spray, or cold spray.
F02C 3/14 - Ensembles fonctionnels de turbines à gaz caractérisés par l'utilisation de produits de combustion comme fluide de travail caractérisés par l'aménagement de la chambre de combustion dans l'ensemble
C22C 30/00 - Alliages contenant moins de 50% en poids de chaque constituant
C23C 4/08 - Matériaux métalliques ne contenant que des éléments métalliques
A method and a system for cold spray deposition of a solid material on a substrate, the system comprising a fluid jet unit; a heating unit; a nozzle, and a powder feeder; the fluid jet unit providing a fluid of a speed up to 1200 m/s and a pressure in a range between 150 and 620 MPa to the heating unit, the heating unit controlling a temperature of the fluid and outputting one of: a superheated and a supercritical fluid; the powder feeder injecting feedstock powder particles into a mixing chamber of the nozzle, the feedstock powder particles being accelerated to a speed above a critical velocity of the feedstock powder particles by the fluid within the nozzle, the nozzle being configured for acceleration of the fluid, mixing the fluid and the feedstock powder particles, and projecting the mixture onto the substrate.
Microfluidic devices, systems and methods are described herein. The devices, systems and methods provide for trapping particles, including cells. Methods of generating a droplet in a microfluidic device and collecting droplets from microfluidic devices are also disclosed herein.
B01L 3/00 - Récipients ou ustensiles pour laboratoires, p. ex. verrerie de laboratoireCompte-gouttes
G01N 15/10 - Recherche de particules individuelles
G01N 15/14 - Techniques de recherche optique, p. ex. cytométrie en flux
G01N 15/149 - Techniques de recherche optique, p. ex. cytométrie en flux spécialement adaptées au tri des particules, p. ex. selon leur taille ou leurs propriétés
The Royal Institution for the Advancement of Learning/McGill Concordia University (Canada)
Concordia University (Canada)
Pratt & Whitney Canada Corp. (Canada)
Inventeur(s)
Larose, Joël
Roy, Amit
Sharifi, Navid
Stoyanov, Pantcho
Moreau, Christian
Chromik, Richard
Makowiec, Mary
Abrégé
A formation method is provided. During this formation method, a metallic substrate is provided. A coating is deposited onto the metallic substrate using a suspension plasma spray process. The coating is formed from or otherwise includes copper oxide.
F01D 11/12 - Prévention ou réduction des pertes internes du fluide énergétique, p. ex. entre étages pour obturations de l'espace entre extrémités d'aubes du rotor et stator utilisant un élément de friction allongé, p. ex. un élément d'usure, déformable ou contraint de façon élastique
12.
APTAMER-BASED ELECTROCHEMICAL DRUG DETECTION ASSAY
Aptamers configured to specifically bind to tetrahydrocannabinol and cannabidiol are disclosed, and biosensing methods and biosensor devices are described in which such aptamers are employed for detection of tetrahydrocannabinol and/or cannabidiol, with a limit of detection in the nanomolar range. In some example implementations, aptamer-based electrochemical biosensors are disclosed for sensitive and rapid detection of tetrahydrocannabinol and/or cannabidiol. Examples of microfluidic biosensors are disclosed that may be utilized in point-of-care settings.
G01N 27/403 - Ensembles de cellules et d'électrodes
G01N 33/53 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet
G01N 33/543 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet avec un support insoluble pour l'immobilisation de composés immunochimiques
G01N 33/94 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des narcotiques
13.
APTAMER-BASED ELECTROCHEMICAL DRUG DETECTION ASSAY
Aptamers configured to specifically bind to tetrahydrocannabinol and cannabidiol are disclosed, and biosensing methods and biosensor devices are described in which such aptamers are employed for detection of tetrahydrocannabinol and/or cannabidiol, with a limit of detection in the nanomolar range. In some example implementations, aptamer-based electrochemical biosensors are disclosed for sensitive and rapid detection of tetrahydrocannabinol and/or cannabidiol. Examples of microfluidic biosensors are disclosed that may be utilized in point-of-care settings.
G01N 27/403 - Ensembles de cellules et d'électrodes
G01N 33/94 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des narcotiques
G01N 33/543 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet avec un support insoluble pour l'immobilisation de composés immunochimiques
A method and a system for cold spray deposition of a solid material on a substrate, the system comprising a fluid jet unit; a heating unit; a nozzle, and a powder feeder; the fluid jet unit providing a fluid of a speed up to 1200 m/s and a pressure in a range between 150 and 620 MPa to the heating unit, the heating unit controlling a temperature of the fluid and outputting one of: a superheated and a supercritical fluid; the powder feeder injecting feedstock powder particles into a mixing chamber of the nozzle, the feedstock powder particles being accelerated to a speed above a critical velocity of the feedstock powder particles by the fluid within the nozzle, the nozzle being configured for acceleration of the fluid, mixing the fluid and the feedstock powder particles, and projecting the mixture onto the substrate.
A method and a system for cold spray deposition of a solid material on a substrate, the system comprising a fluid jet unit; a heating unit; a nozzle, and a powder feeder; the fluid jet unit providing a fluid of a speed up to 1200 m/s and a pressure in a range between 150 and 620 MPa to the heating unit, the heating unit controlling a temperature of the fluid and outputting one of: a superheated and a supercritical fluid; the powder feeder injecting feedstock powder particles into a mixing chamber of the nozzle, the feedstock powder particles being accelerated to a speed above a critical velocity of the feedstock powder particles by the fluid within the nozzle, the nozzle being configured for acceleration of the fluid, mixing the fluid and the feedstock powder particles, and projecting the mixture onto the substrate.
METHOD OF AND SYSTEM FOR PROVIDING AN AGGREGATED MACHINE LEARNING MODEL IN A FEDERATED LEARNING ENVIRONMENT AND DETERMINING RELATIVE CONTRIBUTION OF LOCAL DATASETS THERETO
A method and system are disclosed for providing an aggregated trained machine learning model for performing a prediction task. A main processing device obtains from a first processing device at least a portion of a first trained model having been generated by training an initial model on a first training dataset, and a first training parameter indicative of a level of predictive uncertainty thereof. The main processing device obtains from a second processing device at least a portion of a second trained model having been generated by training the initial model on a second training dataset, and a second training parameter indicative of a level of predictive uncertainty thereof. The main processing device combines, using the first and second training parameters, at least the portion of the first and second trained models to thereby obtain the aggregated trained model. The main processing device provides the aggregated trained model.
The present disclosure relates to fused N-arylsulfonamidyl-thienoisoquinoline compounds, derivatives and pharmaceutical compositions thereof, and methods and uses in inhibiting cancer cell growth, along with a supplemental anti-cancer agent. Centrosome targeting and microtubule depolymerisation are attractive in designing the present chemotherapeutic compounds. The various diseases and conditions treated include various types of cell cancers, and in vitro inhibition.
C07D 491/048 - Systèmes condensés en ortho avec un seul atome d'oxygène comme hétéro-atome du cycle contenant de l'oxygène le cycle contenant de l'oxygène étant à cinq chaînons
The present disclosure relates to fused N-arylsulfonamidyl-thienoisoquinoline compounds, derivatives and pharmaceutical compositions thereof, and methods and uses in inhibiting cancer cell growth, along with a supplemental anti-cancer agent. Centrosome targeting and microtubule depolymerisation are attractive in designing the present chemotherapeutic compounds. The various diseases and conditions treated include various types of cell cancers, and in vitro inhibition.
A61K 31/4436 - Pyridines non condenséesLeurs dérivés hydrogénés contenant d'autres systèmes hétérocycliques contenant un hétérocycle avec le soufre comme hétéro-atome du cycle
The present invention relates to novel polypeptides and enzymes (e.g., thermostable proteins and enzymes) having activities relating to biomass processing and/or degradation (e.g., cell wall deconstruction), as well as polynucleotides, vectors, cells, compositions and tools relating to same, or functional variants thereof. More particularly, the present invention relates to secreted enzymes that may be isolated from the fungi Remersonia thermophila (Stilbella thermophila) strain ATCC 22073, Melanocarpus albomyces strain ATCC 6460, and Lentinula edodes strain ATCC 48564. Uses thereof in various industrial processes such as in biofuels, food preparation, animal feed, pulp and paper, textiles, detergents, waste treatment and others are also disclosed.
The present invention relates to novel polypeptides and enzymes (e.g., thermostable proteins and enzymes) having activities relating to biomass processing and/or degradation (e.g., cell wall deconstruction), as well as polynucleotides, vectors, cells, compositions and tools relating to same, or functional variants thereof. More particularly, the present invention relates to secreted enzymes that may be isolated from the fungi Rhizomucor miehei strain CBS 182.67, Thermoascus thermophilus (Dactylomyces thermophilus) strain ATCC 26413, and Humicola hyalothermophila strain CBS 454.80. Uses thereof in various industrial processes such as in biofuels, food preparation, animal feed, pulp and paper, textiles, detergents, waste treatment and others are also disclosed.
The present invention relates to novel polypeptides and enzymes (e.g., thermostable proteins and enzymes) having activities relating to biomass processing and/or degradation (e.g., cell wall deconstruction), as well as polynucleotides, vectors, cells, compositions and tools relating to same, or functional variants thereof. More particularly, the present invention relates to secreted enzymes that may be isolated from the fungi Chaetomium olivicolor strain CBS 102434, Acremonium thermophilum strain ATCC 24622, and Myceliophthora hinnulea strain ATCC 52474. Uses thereof in various industrial processes such as in biofuels, food preparation, animal feed, pulp and paper, textiles, detergents, waste treatment and others are also disclosed.
C07K 14/37 - Peptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant de champignons
C12N 1/15 - ChampignonsLeurs milieux de culture modifiés par l'introduction de matériel génétique étranger
C12N 1/21 - BactériesLeurs milieux de culture modifiés par l'introduction de matériel génétique étranger
C12N 15/31 - Gènes codant pour des protéines microbiennes, p. ex. entérotoxines
C12N 15/56 - Hydrolases (3) agissant sur les composés glycosyliques (3.2), p. ex. amylase, galactosidase, lysozyme
C12N 15/63 - Introduction de matériel génétique étranger utilisant des vecteursVecteurs Utilisation d'hôtes pour ceux-ciRégulation de l'expression
C12N 15/80 - Vecteurs ou systèmes d'expression spécialement adaptés aux hôtes eucaryotes pour champignons
C12N 9/00 - Enzymes, p. ex. ligases (6.)ProenzymesCompositions les contenantProcédés pour préparer, activer, inhiber, séparer ou purifier des enzymes
C12N 9/24 - Hydrolases (3.) agissant sur les composés glycosyliques (3.2)
C12P 19/00 - Préparation de composés contenant des radicaux saccharide
C12P 21/02 - Préparation de peptides ou de protéines comportant une séquence connue de plusieurs amino-acides, p. ex. glutathion
C12P 7/06 - Éthanol en tant que produit chimique et non en tant que boisson alcoolique
D06M 16/00 - Traitement biochimique des fibres, fils, filés, tissus ou articles fibreux faits de ces matières, p. ex. enzymatique
D21C 1/00 - Traitement préalable des matériaux finement divisés avant la cuisson
D21C 9/00 - Post-traitement de la pâte de cellulose, p. ex. de la pâte de bois, ou des linters de coton
39.
Methods for fabricating morphologically transformed nano-structures (MTNS) and tunable nanocomposite polymer materials, and devices using such materials
In order to implement a microfluidics sensor having higher efficiency, Applicants have developed a method of formation of nano-structures having various shapes and sizes onto materials such as polymers, glass and silicon, which are compatible with the microfabrication processes. The adhesion of the nano-structures and feasibility to tune their properties (optical, electrical and mechanical) are two prime concerns when they are adopted for microfluidics devices.
B01L 3/00 - Récipients ou ustensiles pour laboratoires, p. ex. verrerie de laboratoireCompte-gouttes
B22F 1/00 - Poudres métalliquesTraitement des poudres métalliques, p. ex. en vue de faciliter leur mise en œuvre ou d'améliorer leurs propriétés
B22F 9/24 - Fabrication des poudres métalliques ou de leurs suspensionsAppareils ou dispositifs spécialement adaptés à cet effet par un procédé chimique avec réduction de mélanges métalliques à partir de mélanges métalliques liquides, p. ex. de solutions
C08J 5/00 - Fabrication d'objets ou de matériaux façonnés contenant des substances macromoléculaires
H01B 1/22 - Matériau conducteur dispersé dans un matériau organique non conducteur le matériau conducteur comportant des métaux ou des alliages
B82Y 30/00 - Nanotechnologie pour matériaux ou science des surfaces, p. ex. nanocomposites
B82Y 40/00 - Fabrication ou traitement des nanostructures
G01N 21/33 - CouleurPropriétés spectrales, c.-à-d. comparaison de l'effet du matériau sur la lumière pour plusieurs longueurs d'ondes ou plusieurs bandes de longueurs d'ondes différentes en recherchant l'effet relatif du matériau pour les longueurs d'ondes caractéristiques d'éléments ou de molécules spécifiques, p. ex. spectrométrie d'absorption atomique en utilisant la lumière ultraviolette
G01N 33/543 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet avec un support insoluble pour l'immobilisation de composés immunochimiques
The present invention relates to novel polypeptides and enzymes (e.g., thermostable proteins and enzymes) having activities relating to biomass processing and/or degradation (e.g., cell wall deconstruction), as well as polynucleotides, vectors, cells, compositions and tools relating to same, or functional variants thereof. More particularly, the present invention relates to secreted enzymes that may be isolated from the fungi Chaetomium thermophilum strain ATCC 16451, Thermomyces stellatus strain CBS 241.64, and Corynascus sepedonium strain ATCC 9787. Uses thereof in various industrial processes such as in biofuels, food preparation, animal feed, pulp and paper, textiles, detergents, waste treatment and others are also disclosed.
C12P 19/00 - Préparation de composés contenant des radicaux saccharide
C12P 19/14 - Préparation de composés contenant des radicaux saccharide préparés par action d'une carbohydrase, p. ex. par action de l'alpha-amylase
C12P 21/02 - Préparation de peptides ou de protéines comportant une séquence connue de plusieurs amino-acides, p. ex. glutathion
C12P 7/10 - Éthanol en tant que produit chimique et non en tant que boisson alcoolique préparé comme sous-produit, ou préparé à partir d'un substrat constitué par des déchets ou par des matières cellulosiques d'un substrat constitué par des matières cellulosiques
D06M 16/00 - Traitement biochimique des fibres, fils, filés, tissus ou articles fibreux faits de ces matières, p. ex. enzymatique
D21C 9/00 - Post-traitement de la pâte de cellulose, p. ex. de la pâte de bois, ou des linters de coton
The present invention relates to novel polypeptides and enzymes (e.g., thermostable proteins and enzymes) having activities relating to biomass processing and/or degradation (e.g., cell wall deconstruction), as well as polynucleotides, vectors, cells, compositions and tools relating to same, or functional variants thereof. More particularly, the present invention relates to secreted enzymes that may be isolated from the fungi, Malbranchea cinnamomea strain CBS 343.55, Thielavia australiensis strain ATCC 28236, and Paecilomyces byssochlamydoides strain NRRL 3658. Uses thereof in various industrial processes such as in biofuels, food preparation, animal feed, pulp and paper, textiles, detergents, waste treatment and others are also disclosed.
METHODS FOR FABRICATING MORPHOLOGICALLY TRANSFORMED NANO-STRUCTURES (MTNS) AND TUNABLE NANOCOMPOSITE POLYMER MATERIALS, AND DEVICES USING SUCH MATERIALS
In order to implement a microfluidics sensor having higher efficiency, Applicants have developed a method of formation of nano- structures having various shapes and sizes onto materials such as polymers, glass and silicon, which are compatible with the microfabrication processes. The adhesion of the nano-structures and feasibility to tune their properties (optical, electrical and mechanical) are two prime concerns when they are adopted for microfluidics devices.
C08J 5/04 - Renforcement des composés macromoléculaires avec des matériaux fibreux en vrac ou en nappes
B22F 9/18 - Fabrication des poudres métalliques ou de leurs suspensionsAppareils ou dispositifs spécialement adaptés à cet effet par un procédé chimique avec réduction de mélanges métalliques
B82Y 30/00 - Nanotechnologie pour matériaux ou science des surfaces, p. ex. nanocomposites
B82Y 40/00 - Fabrication ou traitement des nanostructures
C08J 3/20 - Formation de mélanges de polymères avec des additifs, p. ex. coloration
C08J 3/24 - Réticulation, p. ex. vulcanisation, de macromolécules
G01N 21/01 - Dispositions ou appareils pour faciliter la recherche optique
G01N 21/25 - CouleurPropriétés spectrales, c.-à-d. comparaison de l'effet du matériau sur la lumière pour plusieurs longueurs d'ondes ou plusieurs bandes de longueurs d'ondes différentes
G01N 33/48 - Matériau biologique, p. ex. sang, urineHémocytomètres
46.
CELL WALL DECONSTRUCTION ENZYMES OF PAECILOMYCES BYSSOCHLAMYDOIDES AND USES THEREOF
The present invention relates to a process for degrading biomass or pretreated biomass to sugars wherein an enzyme is used comprising a.a polypeptide comprising an amino acid sequence of any one of SEQ ID NOs: or 6; b.a polypeptide comprising an amino acid sequence that is at least 85%, preferably at least 90%, more preferably at least 95%, even more preferably at least 96%, 97%, 98% or 99%amino acid sequence identity to the polypeptide defined in (a); c.a polypeptide comprising an amino acid sequence encoded by the nucleic acid sequence of any one of SEQ ID NOs: 1-4; d.a polypeptide comprising an amino acid sequence encoded by a polynucleotide molecule that hybridizes under medium-high stringency conditions, high stringency conditions, or very high stringency conditions with the full-length complement of a polynucleotide molecule comprising the nucleic acid sequence of any one of SEQ ID NOs: 1-4; e.a polypeptide comprising an amino acid sequence encoded by a polynucleotide molecule having at least 85%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% nucleic acid sequence identity to a polynucleotide comprising the nucleic acid sequence of any one of SEQ ID NOs: 1-4; or f.a polypeptide comprising an amino acid sequence encoded by any one of the exonic nucleic acid sequences corresponding to positions: 1-60, 139-278, 341-385, 445- 497, 556-2834 of SEQ ID NO: 1; 1-101, 154-823 SEQ ID NO: 2.
C12P 19/14 - Préparation de composés contenant des radicaux saccharide préparés par action d'une carbohydrase, p. ex. par action de l'alpha-amylase
C12N 9/24 - Hydrolases (3.) agissant sur les composés glycosyliques (3.2)
C12P 7/10 - Éthanol en tant que produit chimique et non en tant que boisson alcoolique préparé comme sous-produit, ou préparé à partir d'un substrat constitué par des déchets ou par des matières cellulosiques d'un substrat constitué par des matières cellulosiques
47.
CELL WALL DECONSTRUCTION ENZYMES OF MALBRANCHEA CINNAMOMEA AND USES THEREOF
The present invention relates to a novel process for degrading biomass or pretreated biomass to sugars wherein an enzyme is used comprising: a. a polypeptide comprising an amino acid sequence of any one of SEQ ID NOs: 5 or 6; b. a polypeptide comprising an amino acid sequence that is at least 70%, preferably at least 80%, more preferably at least 90%, even more preferably at least 95%, 96%, 97%, 98% or 99% amino acid sequence identity to the polypeptide defined in (a); c. a polypeptide comprising an amino acid sequence encoded by the nucleic acid sequence of any one of SEQ ID NOs: 1-4; d. a polypeptide comprising an amino acid sequence encoded by a polynucleotide molecule that hybridizes under medium-high stringency conditions, high stringency conditions, or very high stringency conditions with the full-length complement of a polynucleotide molecule comprising the nucleic acid sequence of any one of SEQ ID NOs: 1-4; e. a polypeptide comprising an amino acid sequence encoded by a polynucleotide molecule having at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% nucleic acid sequence identity to a polynucleotide comprising the nucleic acid sequence of any one of SEQ ID NOs: 1-4; or f. a polypeptide comprising an amino acid sequence encoded by any one of the exonic nucleic acid sequences corresponding to positions: 1-194, 276-568, 639-809, 869-1143, 1235-1322, 1386-1797, 1872-2040of SEQ ID NO: 1; 1-729 of SEQ ID NO: 2.
C12P 19/14 - Préparation de composés contenant des radicaux saccharide préparés par action d'une carbohydrase, p. ex. par action de l'alpha-amylase
C12N 9/24 - Hydrolases (3.) agissant sur les composés glycosyliques (3.2)
C12P 7/10 - Éthanol en tant que produit chimique et non en tant que boisson alcoolique préparé comme sous-produit, ou préparé à partir d'un substrat constitué par des déchets ou par des matières cellulosiques d'un substrat constitué par des matières cellulosiques
48.
NOVEL CELL WALL DECONSTRUCTION ENZYMES OF THIELAVIA AUSTRALIENSIS AND USES THEREOF
The present invention relates to a novel process for degrading biomass or pretreated biomass to sugars wherein an enzyme is used comprising a. a polypeptide comprising an amino acid sequence of any one of SEQ ID NOs: 7- 9; b. a polypeptide comprising an amino acid sequence that is at least 85%, preferably at least 90%, more preferably at least 95%, even more preferably at least 96%, 97%, 98% or 99% amino acid sequence identity to the polypeptide defined in (a); c. a polypeptide comprising an amino acid sequence encoded by the nucleic acid sequence of any one of SEQ ID NOs: 1 -6; d. a polypeptide comprising an amino acid sequence encoded by a polynucleotide molecule that hybridizes under medium-high stringency conditions, high stringency conditions, or very high stringency conditions with the full-length complement of a polynucleotide molecule comprising the nucleic acid sequence of any one of SEQ ID NOs: 1 -6; e. a polypeptide comprising an amino acid sequence encoded by a polynucleotide molecule having at least 85%, at least 90%, at least 91 %, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% nucleic acid sequence identity to a polynucleotide comprising the nucleic acid sequence of any one of SEQ ID NOs: 1 -6; or f. a polypeptide comprising an amino acid sequence encoded by any one of the exonic nucleic acid sequences corresponding to positions: 1-92, 150-654, 815-1385, 1452-1714 of SEQ ID NO: 2; 1 -246, 324-1007, 1082-1 135 of SEQ ID NO: 1; 1-394, 506-789 of SEQ ID NO: 3.
C12P 19/14 - Préparation de composés contenant des radicaux saccharide préparés par action d'une carbohydrase, p. ex. par action de l'alpha-amylase
C13K 1/02 - GlucoseSirops glucosés obtenus par saccharification de matières cellulosiques
C12N 9/42 - Hydrolases (3.) agissant sur les composés glycosyliques (3.2) agissant sur les liaisons bêta-glucosidiques-1, 4, p. ex. cellulase
C12P 7/10 - Éthanol en tant que produit chimique et non en tant que boisson alcoolique préparé comme sous-produit, ou préparé à partir d'un substrat constitué par des déchets ou par des matières cellulosiques d'un substrat constitué par des matières cellulosiques
49.
NOVEL CELL WALL DECONSTRUCTION ENZYMES OF AMORPHOTHECA RESINAE, RHIZOMUCOR PUSILLUS, AND CALCARISPORIELLA THERMOPHILA, AND USES THEREOF
The present invention relates to novel polypeptides and enzymes (e.g., thermostable proteins and enzymes) having activities relating to biomass processing and/or degradation (e.g., cell wall deconstruction), as well as polynucleotides, vectors, cells, compositions and tools relating to same, or functional variants thereof. More particularly, the present invention relates to secreted enzymes that may be isolated from the fungi, Amorphotheca resinae strain DAOM194228, Rhizomucor pusillus strain CBS 183.67, and Calcarisporiella thermophila strain CBS 279.70. Uses thereof in various industrial processes such as in biofuels, food preparation, animal feed, pulp and paper, textiles, detergents, waste treatment and others are also disclosed.
C12P 7/06 - Éthanol en tant que produit chimique et non en tant que boisson alcoolique
D06M 16/00 - Traitement biochimique des fibres, fils, filés, tissus ou articles fibreux faits de ces matières, p. ex. enzymatique
D06P 5/00 - Autres caractéristiques de la teinture ou de l'impression des textiles ou de la teinture du cuir, des fourrures ou des substances macromoléculaires de toutes formes
D21B 1/02 - Traitement préalable des matières premières par des moyens chimiques ou physiques
D21C 5/00 - Autres procédés pour obtenir de la cellulose, p. ex. cuisson des linters de coton
D21C 9/00 - Post-traitement de la pâte de cellulose, p. ex. de la pâte de bois, ou des linters de coton
50.
CELL WALL DECONSTRUCTION ENZYMES OF PSEUDOCERCOSPORELLA HERPOTRICHOIDES AND|USES THEREOF
The present invention relates to novel Pseudocercosporella herpotrichoides enzymes or proteins for cell wall deconstruction, polynucleotide sequences encoding the polypeptides according to the invention, a production process for the enzymes according to the invention and the use of the enzymes according to the invention in various industrial processes.
C12P 19/14 - Préparation de composés contenant des radicaux saccharide préparés par action d'une carbohydrase, p. ex. par action de l'alpha-amylase
C12P 7/10 - Éthanol en tant que produit chimique et non en tant que boisson alcoolique préparé comme sous-produit, ou préparé à partir d'un substrat constitué par des déchets ou par des matières cellulosiques d'un substrat constitué par des matières cellulosiques
51.
CELL WALL DECONSTRUCTION ENZYMES OF THERMOASCUS AURANTIACUS AND USES THEREOF
The present invention relates tonovel Thermoascus aurantiacus enzymes or proteins for cell wall deconstruction, polynucleotide sequences encoding the polypeptides according to the invention, a production process for the enzymes according to the invention and the use of the enzymes according to the invention in various industrial processes.
C12P 19/14 - Préparation de composés contenant des radicaux saccharide préparés par action d'une carbohydrase, p. ex. par action de l'alpha-amylase
C12P 7/10 - Éthanol en tant que produit chimique et non en tant que boisson alcoolique préparé comme sous-produit, ou préparé à partir d'un substrat constitué par des déchets ou par des matières cellulosiques d'un substrat constitué par des matières cellulosiques
52.
NOVEL CELL WALL DECONSTRUCTION ENZYMES OF THERMOASCUS AURANTIACUS, MYCELIOPHTHORA FERGUSII (CORYNASCUS THERMOPHILUS), AND PSEUDOCERCOSPORELLA HERPOTRICHOIDES, AND USES THEREOF
The present invention relates to novel polypeptides and enzymes (e.g., thermostable proteins and enzymes) having activities relating to biomass processing and/or degradation (e.g., cell wall deconstruction), as well as polynucleotides, vectors, cells, compositions and tools relating to same, or functional variants thereof. More particularly, the present invention relates to secreted enzymes that may be isolated from the fungi, Thermoascus aurantiacus strain CBS 181.67, Myceliophthora fergusii (Corynascus thermophilus) strain CBS 405.69, and Pseudocercosporella herpotrichoides strain 494.80. Uses thereof in various industrial processes such as in biofuels, food preparation, animal feed, pulp and paper, textiles, detergents, waste treatment and others are also disclosed.
C12P 7/06 - Éthanol en tant que produit chimique et non en tant que boisson alcoolique
D06M 16/00 - Traitement biochimique des fibres, fils, filés, tissus ou articles fibreux faits de ces matières, p. ex. enzymatique
D06P 5/00 - Autres caractéristiques de la teinture ou de l'impression des textiles ou de la teinture du cuir, des fourrures ou des substances macromoléculaires de toutes formes
D21C 5/00 - Autres procédés pour obtenir de la cellulose, p. ex. cuisson des linters de coton
D21C 9/00 - Post-traitement de la pâte de cellulose, p. ex. de la pâte de bois, ou des linters de coton
53.
CELL WALL DECONSTRUCTION ENZYMES OF MYCELIOPHTHORA FERGUSII (CORYNASCUS THERMOPHILUS) AND USES THEREOF
The present invention relates to novel Myceliophthora fergusii (Corynascus thermophilus) enzymes or proteins for cell wall deconstruction, polynucleotide sequences encoding the polypeptides according to the invention, a production process for the enzymes according to the invention and the use of the enzymes according to the invention in various industrial processes.
C12P 19/14 - Préparation de composés contenant des radicaux saccharide préparés par action d'une carbohydrase, p. ex. par action de l'alpha-amylase
C12P 7/10 - Éthanol en tant que produit chimique et non en tant que boisson alcoolique préparé comme sous-produit, ou préparé à partir d'un substrat constitué par des déchets ou par des matières cellulosiques d'un substrat constitué par des matières cellulosiques
The present invention relates to novel polypeptides and enzymes (e.g., thermostable proteins and enzymes) having activities relating to biomass processing and/or degradation (e.g., cell wall deconstruction), as well as polynucleotides, vectors, cells, compositions and tools relating to same, or functional variants thereof. More particularly, the present invention relates to secreted enzymes that may be isolated from the fungi, Scytalidium thermophilum strain CBS 625.91, Myriococcum thermophilum strain CBS 389.93, and Aureobasidium pullulans strain ATCC 62921. Uses thereof in various industrial processes such as in biofuels, food preparation, animal feed, pulp and paper, textiles, detergents, waste treatment and others are also disclosed.
The present invention relates to a process for degrading biomass or pretreated biomass wherein an enzyme is used comprising a polypeptide having a. a polypeptide sequence as set forth in any one of SEQ ID Nos: 3, 6, 9, 12, 15, 8, 21, 24, 27, 30, 33, 36, 39, 42, 45, 48, 51, 54, 57, 59, 61, 63, 65, 67, 69 and 71; b. a polypeptide that is at least 60%, preferably at least 70%, more preferably at least 80%, even more preferably at least 90%, 95%, 96%, 97%, 98% or 99% homologous to the any one of SEQ ID Nos: 3, 6, 9, 12, 15, 18, 21, 24, 27, 30, 33, 36, 39, 42, 45, 48, 51, 54, 57, 59, 61, 63, 65, 67, 69 and 71; c.a polypeptide sequence encoded by nucleic acids sequence as set forth in any one of SEQ ID NOs: 1, 2, 4, 5, 7, 8, 10, 11, 13, 14, 16, 17, 19, 20, 22, 23, 25, 26, 28, 29, 31, 32, 34, 35, 37, 38, 40, 41, 43, 44, 46, 47, 49, 50, 52, 53, 56, 58,60, 62, 64, 66, 68 and 70, or nucleic acids that are at least 60%, preferably at least 70%, more preferably at least 80%, even more preferably at least 90%, 95%, 96%, 97%, 98% or 99% homologous to any one of SEQ ID NOs: 1, 2, 4, 5, 7, 8, 10, 11, 13, 14, 16, 17, 19, 20, 22, 23, 25, 26, 28, 29, 31, 32, 34, 35, 37, 38, 40, 41, 43, 44, 46, 47, 49, 50, 52, 53, 56, 58, 60, 62, 64, 66, 68 and 70; d.a polypeptide sequence encoded by a nucleic acids sequence hybridizing under stringent conditions to the polynucleotide as set forth in any one of 2 SEQ ID NOs: 1, 2, 4, 5, 7, 8, 10, 11, 13, 14, 16, 17, 19, 20, 22, 23, 25, 26, 28, 29, 31, 32, 34, 35, 37, 38, 40, 41, 43, 44, 46, 47, 49, 50, 52, 53, 55, 56, 58, 60, 62, 64, 66, 68 and 70; or e.a polypeptide sequence encoded by a nucleic acids sequence hybridizing under stringent conditions to the reverse complement of a polynucleotide as set forth in any one of SEQ ID NOs: 1, 2, 4, 5, 7, 8, 10, 11, 13, 14, 16, 17, 19, 20, 22, 23, 25, 26, 28, 29, 31, 32, 34, 35, 37, 38, 40, 41, 43, 44, 46, 47, 49, 50, 52, 53, 56, 58, 60, 62, 64, 66, 68 and70.
The present invention relates to process for degrading biomass or pretreated biomass to sugars wherein an enzyme is used comprising a polypeptide having a. a polypeptide sequence as set forth in any one of SEQ ID Nos:3, 6, 9, 12, 15, 18, 21, 24, 27, 30, 33, 36, 39, 42, 45, 48, 51, 54, 57, 60, 62 and 64; b. a polypeptide that is at least 60%, preferably at least 70%, more preferably at least 80%, even more preferably at least 90%, 95%, 96%, 97%, 98% or 99% homologous to the any one of SEQ ID Nos:3, 6, 9, 12, 15, 18, 21, 24, 27, 30, 33, 36, 39, 42, 45, 48, 51, 54, 57, 60, 62 and 64; c. a polypeptide sequence encoded by nucleic acids sequence as set forth in any one of SEQ ID NOs: 1, 2, 4, 5, 7, 8, 10, 11, 13, 14, 16, 7, 19, 20, 22, 23, 25, 26, 28, 29, 31, 32, 34, 35, 37, 38, 40, 41, 43, 44, 46, 47, 49, 50, 52, 53, 55, 56, 58, 59, 61 and 63, or nucleic acids that are at least 60%, preferably at least 70%, more 2 preferably at least 80%, even more preferably at least 90%, 95%, 96%, 97%, 98% or 99% homologous to any one of SEQ ID NOs: 1, 2, 4, 5, 7, 8, 10, 11, 13, 14, 16, 17, 19, 20, 22, 23, 25, 26, 28, 29, 31, 32, 34, 35, 37, 38, 40, 41, 43, 44, 46, 47, 49, 50, 52, 53, 55, 56, 8, 59, 61 and 63;30 d. a polypeptide sequence encoded by a nucleic acids sequence hybridizing under stringent conditions to the polynucleotide as set DSM IP Assets B.V. 28984-WO-PCT forth in any one of SEQ ID NOs: 1, 2, 4, 5, 7, 8, 10, 11, 13, 14, 16, 7, 19, 20, 22, 23, 25, 26, 28, 29, 31, 32, 34, 35, 37, 38, 40, 41, 43, 44, 46, 47, 49, 50, 52, 53, 55, 56, 58, 59, 61 and 63; or e. a polypeptide sequence encoded by a nucleic acids sequence hybridizing under stringent conditions to the reverse complement of a polynucleotide as set forth in any one of SEQ ID NOs: 1, 2, 4, 5, 7, 8, 10, 11, 13, 14, 16, 17, 19, 20, 22, 23, 25, 26, 28, 29, 31, 32, 34, 35, 37, 38, 40, 41, 43, 44, 46, 47, 49, 50,52, 53, 55, 56, 58, 59, 61 and 63.
The present invention relates to process for degrading biomass or pretreated biomass to sugars wherein an enzyme is used comprising a polypeptide having a.a polypeptide sequence as set forth in any one of SEQ ID Nos:3, 6, 9, 12, 15, 18, 21, 24, 27, 30, 33, 36, 39, 42, 44, 47 and 50; b.a polypeptide that is at least 60%, preferably at least 70%, more preferably at least 80%, even more preferably at least 90%, 95%, 96%, 97%,98% or 99% homologous to the any one of SEQ ID Nos:3, 6, 9, 12, 15, 18, 21, 24, 27, 30, 33, 36, 39, 42, 44, 47 and 50; c.a polypeptide sequence encoded by nucleic acids sequence as set forth in any one of SEQ ID NOs: 1, 2, 4, 5, 7, 8, 10, 11, 13, 14, 16, 7, 19, 20, 22, 23, 25, 26, 28, 29, 31, 32, 34, 35, 37, 38, 40, 41, 43, 45, 46, 48 and 50, or nucleic acids that are at least 60%, preferably at least 70%, more preferably at least 80%, even more preferably at least 90%, 95%, 96%, 97%, 98% or 99% homologous to any one of SEQ ID NOs: 1, 2, 4, 5, 7, 8, 10, 11, 13, 14, 16, 17, 9, 20, 22, 23, 25, 26, 28, 29, 31, 32, 34, 35, 37, 38, 40, 41, 43, 45, 46, 48 and 50; d.a polypeptide sequence encoded by a nucleic acids sequence hybridizing under stringent conditions to the polynucleotide as set forth in any one of SEQ ID NOs: 1, 2, 4, 5, 7, 8, 10, 11, 13, 14, 16, 7, 19, 20, 22, 23, 25, 26, 28, 29, 31, 32, 34, 35, 37, 38, 40, 41, 43, 45, 46, 48 and 50; or e.a polypeptide sequence encoded by a nucleic acids sequence hybridizing under stringent conditions to the reverse complement of a polynucleotide as set forth in any one of SEQ ID NOs: 1, 2, 4, 5, 7, 8, 10, 11, 13, 14, 16, 17, 19, 20, 22, 23, 25, 26, 28, 29, 31, 32, 34, 35, 37, 38, 40, 41, 43, 45, 46, 48 and 50.
There is provided a method and system for detecting and locating damages occurring in large structures made of polymer matrix composite materials while the structures are subjected to loading. Carbon nanotubes are added to a resin to make the latter electrically conductive. The modified resin is incorporated with long fibers to make the composite structures, which are marked with grid points where electrically conductive materials are deposited. The electrical resistances and potentials between the grid points for electrically non-conductive fibers and conductive fibers reinforced polymer composite structures are measured and used as a reference set. Since the occurrence of a damage changes the electric resistance and potential between contact points surrounding the damage, such a change serves as an indication of occurrence of the damage. The position of the damage in the structure is also determined. Damages can be detected and located in-situ while the composite structure is in operation.
The present invention relates to novel Thermomyces lanuginosus enzymes or proteins for cell wall deconstruction, polynucleotide sequences encoding the polypeptides according to the invention, a production process for the enzymes according to the invention and the use of the enzymes according to the invention in various industrial processes.
C12N 9/24 - Hydrolases (3.) agissant sur les composés glycosyliques (3.2)
C12N 9/42 - Hydrolases (3.) agissant sur les composés glycosyliques (3.2) agissant sur les liaisons bêta-glucosidiques-1, 4, p. ex. cellulase
C12P 19/00 - Préparation de composés contenant des radicaux saccharide
C12P 7/10 - Éthanol en tant que produit chimique et non en tant que boisson alcoolique préparé comme sous-produit, ou préparé à partir d'un substrat constitué par des déchets ou par des matières cellulosiques d'un substrat constitué par des matières cellulosiques
D06M 16/00 - Traitement biochimique des fibres, fils, filés, tissus ou articles fibreux faits de ces matières, p. ex. enzymatique
D21C 5/00 - Autres procédés pour obtenir de la cellulose, p. ex. cuisson des linters de coton
The present invention relates to a process for degrading biomass or pretreated biomass to sugars wherein an enzyme is used comprising a polypeptide having a. a polypeptide sequence as set forth in any one of SEQ ID Nos: 3, 6, 9, 12, 15, 18, 21, 24, 27, 30, 33, 36, 39 and 42; b. a polypeptide that is at least 60%, preferably at least 70%, more preferably at least 80%, even more preferably at least 90%, 95%, 96%, 97%, 98% or 99% homologous to the any one of SEQ ID Nos: 3, 6, 9, 12, 15, 18, 21, 24, 27, 30, 33, 36, 39 and 42; c. a polypeptide sequence encoded by nucleic acids sequence as set forth in any one of SEQ ID NOs: 1, 2, 4, 5, 7, 8, 10, 11, 13, 14, 16, 17, 19, 20, 22, 23, 25, 26, 28, 29, 31, 32, 34, 35, 37, 38, 40 and 41, or nucleic acids that are at least 60%, preferably at least 70%, more preferably at least 80%, even more preferably at least 90%, 95%, 96%, 97%, 98% or 99% homologous to any one of SEQ ID NOs: 1, 2, 4, 5, 7, 8, 10, 1 1, 13, 14, 16, 17, 19, 20, 22, 23, 25, 26, 28, 29, 31, 32, 34, 35, 37, 38, 40 and 41; d. a polypeptide sequence encoded by a nucleic acids sequence hybridizing under stringent conditions to the polynucleotide as set forth in any one of SEQ ID NOs: 1, 2, 4, 5, 7, 8, 10, 11, 13, 14, 16, 17, 19, 20, 22, 23, 25, 26, 28, 29, 31, 32, 34, 35, 37, 38, 40 and 41; or e. a polypeptide sequence encoded by a nucleic acids sequence hybridizing under stringent conditions to the reverse complement of a polynucleotide as set forth in any one of SEQ ID NOs: 1, 2, 4, 5, 7, 8, 10, 11, 13, 14, 16, 17, 19, 20, 22, 23, 25, 26, 28, 29, 31, 32, 34, 35, 37, 38, 40 and 41.
C12P 7/10 - Éthanol en tant que produit chimique et non en tant que boisson alcoolique préparé comme sous-produit, ou préparé à partir d'un substrat constitué par des déchets ou par des matières cellulosiques d'un substrat constitué par des matières cellulosiques
C12N 9/42 - Hydrolases (3.) agissant sur les composés glycosyliques (3.2) agissant sur les liaisons bêta-glucosidiques-1, 4, p. ex. cellulase
65.
NOVEL CELL WALL DECONSTRUCTION ENZYMES OF THERMOMYCES LANUGINOSUS AND USES THEREOF
The present invention relates to a process for degrading biomass or pretreated biomass to sugars wherein an enzyme is used comprising a polypeptide having a. a polypeptide sequence as set forth in any one of SEQ ID Nos: 3, 6, 9, 12, 15, 18, 21, 24, 27 and 30; b. a polypeptide that is at least 60%, preferably at least 70%, more preferably at least 80%, even more preferably at least 90%, 95%, 96%, 97%, 98% or 99% homologous to the any one of SEQ ID Nos: 3, 6, 9, 12, 15, 18, 21, 24, 27 and 30; c. a polypeptide sequence encoded by nucleic acids sequence as set forth in any one of SEQ ID NOs: 1, 2, 4, 5, 7, 8, 10, 11, 13, 14, 16, 17, 19, 20, 22, 23, 25, 26, 28 and 29, or nucleic acids that are at least 60%, preferably at least 70%, more preferably at least 80%, even more preferably at least 90%, 95%, 96%, 97%, 98% or 99% homologous to any one of SEQ ID NOs: 1, 2, 4, 5, 7, 8, 10, 11, 13, 14, 16, 17, 19, 20, 22, 23, 25, 26, 28 and 29; a polypeptide sequence encoded by a nucleic acids sequence hybridizing under stringent conditions to the polynucleotide as set forth in any one of SEQ ID NOs: 1, 2, 4, 5, 7, 8, 10, 11, 13, 14, 16, 17, 19, 20, 22, 23, 25, 26, 28 and 29; or e. a polypeptide sequence encoded by a nucleic acids sequence hybridizing under stringent conditions to the reverse complement of a polynucleotide as set forth in any one of SEQ ID NOs: 1, 2, 4, 5, 7, 8, 10, 11, 13, 14, 16, 17, 19, 20, 22, 23, 25, 26, 28 and 29.
The present invention relates to novel enzymes or proteins for cell wall deconstruction obtainable from Talaromyces thermophilus, polynucleotide sequences encoding the polypeptides according to the invention, a production process for the enzymes according to the invention and the use of the enzymes according to the invention in various industrial processes.
C12N 9/24 - Hydrolases (3.) agissant sur les composés glycosyliques (3.2)
C12N 9/42 - Hydrolases (3.) agissant sur les composés glycosyliques (3.2) agissant sur les liaisons bêta-glucosidiques-1, 4, p. ex. cellulase
C12P 19/00 - Préparation de composés contenant des radicaux saccharide
C12P 7/10 - Éthanol en tant que produit chimique et non en tant que boisson alcoolique préparé comme sous-produit, ou préparé à partir d'un substrat constitué par des déchets ou par des matières cellulosiques d'un substrat constitué par des matières cellulosiques
D06M 16/00 - Traitement biochimique des fibres, fils, filés, tissus ou articles fibreux faits de ces matières, p. ex. enzymatique
D21C 5/00 - Autres procédés pour obtenir de la cellulose, p. ex. cuisson des linters de coton
The invention provides a fast method for a high-quality interpolation of a finite multidimensional dataset. It has particular application in digital image processing, including, but not limited to, processing of both still images and real-time image/data processing. The method uses discrete cosine and sine transforms of appropriate types to covert, in blocks of desired size, the initial dataset to the frequency domain. Proposed interpolators calculate a chain of inverse transforms of non-square sizes that perform the interpolation. The larger transform is broken into smaller transforms of non-square size using a recursive size reduction process of FFT-type, and the smaller transforms are calculated directly exploiting the symmetry properties of smaller interpolator functions involved. An output dataset is then assembled using the calculated transforms. The method avoids computationally costly process of inflating the coefficient space by padding zeros exploited for DCT-based interpolations previously.
G06K 9/00 - Méthodes ou dispositions pour la lecture ou la reconnaissance de caractères imprimés ou écrits ou pour la reconnaissance de formes, p.ex. d'empreintes digitales
The present invention relates to gene and protein sequences for a thebaine 6-O- demethylase from Papaver somniferum and methods of use therefor. The present invention also relates to gene and protein sequences for a codeine O-demethylase from Papaver somniferum and methods of use therefor. The present invention also relates to gene and protein sequences for a protoberberine 10 O-demethylase from Papaver somniferum and methods of use therefor. In particular, systems for the recombinant production of opiates in yeast and transgenic plants for the production of opiates are provided.
A01H 5/00 - Angiospermes, c.-à-d. plantes à fleurs, caractérisées par leurs parties végétalesAngiospermes caractérisées autrement que par leur taxonomie botanique
C07H 21/00 - Composés contenant au moins deux unités mononucléotide comportant chacune des groupes phosphate ou polyphosphate distincts liés aux radicaux saccharide des groupes nucléoside, p. ex. acides nucléiques
C12N 1/19 - LevuresLeurs milieux de culture modifiés par l'introduction de matériel génétique étranger
C12N 1/21 - BactériesLeurs milieux de culture modifiés par l'introduction de matériel génétique étranger
C12N 15/00 - Techniques de mutation ou génie génétiqueADN ou ARN concernant le génie génétique, vecteurs, p. ex. plasmides, ou leur isolement, leur préparation ou leur purificationUtilisation d'hôtes pour ceux-ci
C12N 15/63 - Introduction de matériel génétique étranger utilisant des vecteursVecteurs Utilisation d'hôtes pour ceux-ciRégulation de l'expression
C12N 9/02 - Oxydoréductases (1.), p. ex. luciférase
C12P 17/18 - Préparation de composés hétérocycliques comportant O, N, S, Se ou Te comme uniques hétéro-atomes du cycle contenant plusieurs hétérocycles condensés entre eux ou condensés avec un système carbocyclique commun, p. ex. rifamycine
78.
NANO-ENHANCED EVANESCENCE INTEGRATED TECHNIQUE (NEET) BASED MICROPHOTONIC DEVICE AND SAMPLE ANALYSIS SYSTEM
A device, a method of fabricating the device and a sample analysis system that includes the device are provided. The device includes an optical waveguide having a plurality of nanofeatures integrated thereon to influence at least one of evanescence and coupling of an optical field of the optical waveguide. The sample analysis system includes a fluidic actuation system for introducing sample specimen fluid into a microfluidic channel of the device for evanescence based detection.
B82B 1/00 - Nanostructures formées par manipulation d’atomes ou de molécules, ou d’ensembles limités d’atomes ou de molécules un à un comme des unités individuelles
G02B 6/12 - Guides de lumièreDétails de structure de dispositions comprenant des guides de lumière et d'autres éléments optiques, p. ex. des moyens de couplage du type guide d'ondes optiques du genre à circuit intégré