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Institution

Novozymes

CompanyCopenhagen, Denmark
About: Novozymes is a company organization based out in Copenhagen, Denmark. It is known for research contribution in the topics: Nucleic acid & Polynucleotide. The organization has 2506 authors who have published 2828 publications receiving 89266 citations. The organization is also known as: Novo Enzymes A/S & Novozymes A/S.


Papers
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Patent
27 Nov 2002
TL;DR: In this paper, mutations of a subtilisin gene result in changes in the chemical characteristics of the enzyme, which is more stable to oxidation, possesses greater protease activity, and exhibits improved washability.
Abstract: The present invention relates to mutations of a subtilisin gene which result in changes in the chemical characteristics of subtilisin enzymes. Mutations at specific nucleic acids of the subtilisin gene result in amino acid substitutions and consequently, altered enzyme function. Some of these mutant enzymes exhibit physical properties advantageous to industrial applications, particularly in the detergent industry, providing subtilisin which is more stable to oxidation, possesses greater protease activity, and exhibits improved washability.

29 citations

Journal ArticleDOI
TL;DR: The adoption of a nomenclatura quimica consensuada is a herramienta clave for la comunicación eficiente en las ciencias quimicas, for the busqueda con ordenadores en bases de datos and con fine regulatorios, tales como los asociados a la salud y la seguridad o a la actividad comercial as discussed by the authors.
Abstract: INTRODUCCION La adopcion universal de una nomenclatura quimica consensuada es una herramienta clave para la comunicacion eficiente en las ciencias quimicas, para la busqueda con ordenadores en bases de datos y con fines regulatorios, tales como los asociados a la salud y la seguridad o a la actividad comercial. La Union Internacional de Quimica Pura y Aplicada (IUPAC en sus siglas inglesas) ofrece recomendaciones sobre la naturaleza y el uso de la nomenclatura quimica. Los fundamentos de esta nomenclatura se muestran aqui y en los documentos complementarios sobre los sistemas de nomenclatura de quimica organica y polimeros, con hipervinculos a los documentos originales. Un resumen general de la nomenclatura quimica se puede encontrar en Principles of Chemical Nomenclature. Detalles mayores se pueden hallar en Nomenclature of Inorganic Chemistry coloquialmente conocido como el Libro Rojo, y en las publicaciones relacionadas con compuestos organicos (el Libro Azul) y polimeros (el Libro Purpura). Cabe senalar que muchos compuestos pueden tener nombres no-sistematicos o semi-sistematicos (algunos de los cuales no son aceptados por la IUPAC, por ejemplo, porque son ambiguos) y las reglas IUPAC permiten dar mas de un nombre sistematico a un compuesto en muchos casos. La IUPAC esta elaborando la identificacion de los nombres individuales preferidos a efectos de regulacion (Preferred IUPAC Names o PINs). Nota: En este documento, el simbolo ‘=’ se utiliza para dividir los nombres que resultan ser demasiado largos para el formato de la columna, a menos que ya haya un guion presente en el nombre. Los limites entre compuestos ‘organicos’ e ‘inorganicos’ son difusos. Los tipos de nomenclatura descritos en este documento son aplicables a los compuestos, moleculas e iones que no contienen carbono y tambien a muchas estructuras que contienen carbono (Seccion 2), principalmente los que contienen elementos de los grupos 1−12. La mayoria de los compuestos de boro se tratan mediante una nomenclatura especial. 8

29 citations

Journal ArticleDOI
TL;DR: The crystallographic and kinetic studies on RGL4, and structural and sequence comparison to other enzymes in the same and other PL families, enable us to propose a detailed reaction mechanism for the β-elimination on [-,2)-α-l-rhamno-(1,4)- α-d-galacturonic acid-(1,-].

29 citations

Journal ArticleDOI
TL;DR: How mucus nanostructure can be modulated by the addition of high-molecular weight HA that offers an opportunity to control mucosal pathogenesis and drug delivery is demonstrated.
Abstract: This study investigates the effects of different molecular weight hyaluronic acids (HAs) on the mucosal nanostructure using a pig stomach mucin hydrogel as a mucosal barrier model. Microparticles (1.0 μm) and nanoparticles (200 nm) were used as probes, and their movement in mucin was studied by a three-dimensional confocal microscopy-based particle tracking technique and by Nanoparticle Tracking Analysis (NTA) after addition of high-molecular weight (900 kDa) and low-molecular weight (33 kDa) HA. This demonstrated a molecular weight-dependent HA modulation of the mucin nanostructure with a 2.5-fold decrease in the mobility of 200 nm nanoparticles. To further investigate these mechanisms and to verify that the natural viscoelastic properties of mucus are not undesirably altered, rheological measurements were performed on mucin hydrogels with or without HA. This suggested the observed particle mobility restriction was not attributed to alterations of the natural mucin cohesive and viscoelastic properties bu...

29 citations

Journal ArticleDOI
TL;DR: Comparisons show type-dependent action modes of TtAA9E and TaAA9A for cellulose oxidation together with substrate-dependent synergistic hydrolysis of cellulosic substrates, suggesting a selection of AA9 proteins specific to substrates is required for industrial utilization.
Abstract: Lytic polysaccharide monooxygenase (LPMO) is a group of recently identified proteins that catalyze oxidative cleavage of the glycosidic linkages of cellulose and other polysaccharides. By utilizing the oxidative mode of action, LPMOs are able to enhance the efficiency of cellulase in the hydrolysis of cellulose. Particularly, auxiliary activity family 9 (AA9) is a group of fungal LPMOs that show a type-dependent regioselectivity on cellulose in which Types 1, 2, and 3 hydroxylate at C1, C4, and C1 and C4 positions, respectively. In this study, we investigated comparative characteristics of TtAA9E from Thielavia terrestris belonging to Type 1 and TaAA9A from Thermoascus aurantiacus belonging to Type 3 on cellulose and pretreated lignocellulose. From product analysis, TtAA9E dominantly generated oligosaccharides with an aldonic acid form, which is an evidence of C1 oxidation, while TaAA9A generated oligosaccharides with both aldonic acid and 4-ketoaldose forms, which is evidence of C1 and C4 oxidations, respectively. For hydrolysis of cellulose (Avicel) by cellulase, higher synergism was observed for TtAA9E than for TaAA9A. For hydrolysis of pretreated lignocellulose using rice straw, synergistic behaviors of TtAA9E and TaAA9A were different depending on the pretreatment of rice straw. Specifically, on acid-pretreated rice straw, TtAA9E showed a higher synergism than TaAA9A while on alkali-pretreated rice straw, TaAA9A showed a higher synergism than TtAA9E. We show type-dependent action modes of TtAA9E and TaAA9A for cellulose oxidation together with substrate-dependent synergistic hydrolysis of cellulosic substrates. The results obtained from this study indicate the different behaviors of AA9s on cellulose and pretreated lignocellulose, suggesting a selection of AA9 proteins specific to substrates is required for industrial utilization.

29 citations


Authors

Showing all 2507 results

NameH-indexPapersCitations
Jens Nielsen1491752104005
Gary K. Schoolnik8123327782
Lubbert Dijkhuizen7542421761
Bauke W. Dijkstra7225619487
Michel Vert6933317899
Henning Langberg6024211999
Harinderjit Gill5931912978
John M. Woodley5842013426
Lei Cai5737416689
Anette Müllertz5727410319
Peter J. Punt521548846
Svein Jarle Horn511239511
Martin Hofrichter501587387
Eva Stoger491278367
Luciano Saso453257672
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20229
202181
202070
201998
2018102
2017135