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Endoglucanase V and a phosphatase from Trichoderma viride are able to act on modified exopolysaccharide from Lactococcus lactis subsp. cremoris B40.Effect of pretreatment severity on xylan solubility and enzymatic breakdown of the remaining cellulose from wheat straw.A comparison of liquid chromatography, capillary electrophoresis, and mass spectrometry methods to determine xyloglucan structures in black currants.Capillary electrophoresis fingerprinting, quantification and mass-identification of various 9-aminopyrene-1,4,6-trisulfonate-derivatized oligomers derived from plant polysaccharides.Bilberry xyloglucan--novel building blocks containing beta-xylose within a complex structure.Boosting LPMO-driven lignocellulose degradation by polyphenol oxidase-activated lignin building blocksH2O2 as a candidate bottleneck for MnP activity during cultivation of Agaricus bisporus in compost.Biochemical characterization and relative expression levels of multiple carbohydrate esterases of the xylanolytic rumen bacterium Prevotella ruminicola 23 grown on an ester-enriched substrate.Characterization and mode of action of two acetyl xylan esterases from Chrysosporium lucknowense C1 active towards acetylated xylans.Carbohydrate utilization and metabolism is highly differentiated in Agaricus bisporus.Uncovering the abilities of Agaricus bisporus to degrade plant biomass throughout its life cycle.Compost Grown Agaricus bisporus Lacks the Ability to Degrade and Consume Highly Substituted Xylan Fragments.Accumulation of recalcitrant xylan in mushroom-compost is due to a lack of xylan substituent removing enzyme activities of Agaricus bisporus.Fate of Carbohydrates and Lignin during Composting and Mycelium Growth of Agaricus bisporus on Wheat Straw Based Compost.β-Glucans and Resistant Starch Alter the Fermentation of Recalcitrant Fibers in Growing Pigs.Occurrence and function of enzymes for lignocellulose degradation in commercial Agaricus bisporus cultivation.Lytic polysaccharide monooxygenases from Myceliophthora thermophila C1 differ in substrate preference and reducing agent specificity.Discovery of the combined oxidative cleavage of plant xylan and cellulose by a new fungal polysaccharide monooxygenase.Characterisation of non-degraded oligosaccharides in enzymatically hydrolysed and fermented, dilute ammonia-pretreated corn stover for ethanol productionCE-MSn of complex pectin-derived oligomers.Potential of a gypsum-free composting process of wheat straw for mushroom productionQuantification of Lignin and Its Structural Features in Plant Biomass Using 13C Lignin as Internal Standard for Pyrolysis-GC-SIM-MSEnzyme resistant feruloylated xylooligomer analogues from thermochemically treated corn fiber contain large side chains, ethyl glycosides and novel sites of acetylation.In vitro fermentability of differently substituted xylo-oligosaccharides.Location of O-acetyl substituents in xylo-oligosaccharides obtained from hydrothermally treated Eucalyptus wood.Carbohydrate composition of compost during composting and mycelium growth of Agaricus bisporus.Separation of digesta fractions complicates estimation of ileal digestibility using marker methods with Cr2O3 and cobalt-ethylenediamine tetraacetic acid in broiler chickens.Processing technologies and cell wall degrading enzymes to improve nutritional value of dried distillers grain with solubles for animal feed: an in vitro digestion study.Standard assays do not predict the efficiency of commercial cellulase preparations towards plant materials.Effects of Eucalyptus globulus wood autohydrolysis conditions on the reaction products.RP-UHPLC-UV-ESI-MS/MS analysis of LPMO generated C4-oxidized gluco-oligosaccharides after non-reductive labeling with 2-aminobenzamide.Quantification of the catalytic performance of C1-cellulose-specific lytic polysaccharide monooxygenases.Lignin composition is more important than content for maize stem cell wall degradation.Laccase/Mediator Systems: Their Reactivity toward Phenolic Lignin Structures.The physiology of Agaricus bisporus in semi-commercial compost cultivation appears to be highly conserved among unrelated isolates.A novel acetyl xylan esterase enabling complete deacetylation of substituted xylans.Distinct Substrate Specificities and Electron-Donating Systems of Fungal Lytic Polysaccharide Monooxygenases.Hydrothermal processing of rice husks: effects of severity on product distributionHydrothermally treated xylan rich by-products yield different classes of xylo-oligosaccharidesBiomass Pretreatment and Enzymatic Hydrolysis Dynamics Analysis Based on Particle Size Imaging
P50
Q30761301-743D0CCF-5E21-40D4-8B5D-7E1943D82999Q30827468-F6D65750-D440-465D-BF40-5120E58F08C9Q33256891-3EC63F3A-0525-4106-9B05-D38FF5A93D92Q33263062-4FB0EABB-26FF-4D80-81D7-BF4130A716CEQ33268249-354A7D77-3183-4864-BC97-245F55277925Q33654888-7A92D490-8C3A-4AAE-A0AD-9BCBE9AB6F42Q33808817-717C1B7D-9945-43F2-AEA8-E5AD24B12AA4Q33956660-E0EE411F-2738-4E37-BF4F-67B4CAE2DD1EQ34082324-C94EAD76-3865-4ECE-B1DF-4F52CE1270C4Q35001395-05280EFB-CABB-472B-B3E2-4902E5ECD5C1Q35676450-98B087A8-DBDA-4E29-8C31-37BCA4B7BB86Q35735213-31300D37-9C82-4A30-9BCA-E7D42B01E4B9Q35740834-4745CC3F-392B-41B6-B2BF-EAE887EF5397Q35799084-6ECBB9BA-E320-4CC0-A687-233673B1DEC8Q36211958-9A66B542-0F77-453F-B1B6-00C5648D2598Q36361473-3094711F-EE61-4120-A752-6A40CEECD2D6Q40992538-46A5680A-B3DA-4984-BD73-BB9D6FB3A7E4Q41736451-28459FB1-EF75-4665-9097-7A306FCB66F0Q42038325-13391511-379A-475B-8B34-32FF154F226BQ42162836-9C3F839F-CFF2-4E9A-A62D-C30F515D4C9CQ42370791-7BA03A61-C983-4541-88DA-846D0101FCBCQ42380256-71D0E88E-E88F-469A-99D1-5417F9F2025BQ43808975-EB08FC93-D75B-4F40-9F7C-EF48D3ED24DDQ44162825-CA70D198-6855-4ACC-98A6-EB9E7A0F8442Q44264093-FD55731D-9699-4C53-80C8-105BABFF5417Q44276503-BA235FA3-60EA-4A5C-841A-AD90107F6078Q45202653-4321D6E6-3D53-47EC-8D50-D53E0980A211Q45907212-3AE71F25-1ED0-474A-B21E-8ADE9F332C5FQ46729323-66E56AB5-4D31-4C50-A282-115A95E1B18DQ46978328-8EC4427F-8F3A-4BFA-A58D-29F14EE451B7Q47836860-D145CE4A-D197-4D4C-8D77-4B148C1D0429Q48192965-13AE80F2-6E79-417E-9C1F-35E9983F37F0Q48194136-1E55758E-CB8A-4A0A-9E79-6827B38E3263Q49521724-F0FE6121-22C5-4C5C-8382-5F2FBC9BCFFCQ49579213-C5E56511-6B92-426B-87A0-07DE445AC272Q52626602-81151C9B-213A-4AE3-9732-A7251BDDB748Q55491783-1CD74D73-465E-4382-B22B-BE190237B0EDQ56954927-BA506D8D-789A-490A-BB27-E970AB604F01Q56955247-EE8D7EB0-5BDC-4888-A402-B7E2BDFF58A1Q58598566-016E993B-2B15-4169-B0CD-C0E74764911E
P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Mirjam A. Kabel
@en
Mirjam A. Kabel
@es
Mirjam A. Kabel
@sl
Mirjam Kabel
@nl
type
label
Mirjam A. Kabel
@en
Mirjam A. Kabel
@es
Mirjam A. Kabel
@sl
Mirjam Kabel
@nl
altLabel
M. Kabel
@nl
M.A. Kabel
@nl
Mirjam A. Kabel
@nl
prefLabel
Mirjam A. Kabel
@en
Mirjam A. Kabel
@es
Mirjam A. Kabel
@sl
Mirjam Kabel
@nl
P1053
M-1051-2016
P106
P1153
6602821522
P21
P31
P3829
P496
0000-0002-2787-7852
P7449
PRS1282582