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1 ous fungi (hydrophobin HFBI from Trichoderma reesei).
2 cellobiohydrolase I (CBH I) from Trichoderma reesei.
3 dustrial enzyme-producing fungus Trichoderma reesei.
4 cellulose-degrading model fungus Trichoderma reesei.
5 s fungi Fusarium graminearum and Trichoderma reesei.
6 (E212Q) of the enzyme Cel7A from Trichoderma reesei.
7 s, we found and demonstrate (for Trichoderma reesei) alternative, overlapping internal introns.
8 beta-mannanase was isolated from Trichoderma reesei and expressed via the chloroplast genome.
9 ngal family AA9 LPMOs, TrAA9A of Trichoderma reesei and NcAA9C of Neurospora crassa, and two bacteria
10 gest inhibitory activity against Trichoderma reesei and Pseudomonas solancearum.
11 7 GH7 CBH genes was expressed in Trichoderma reesei and screened using a multiplexed activity screeni
12 d into P. funiculosum cel7a, expressed in T. reesei, and assayed on lignocellulosic biomass.
13  enzyme cocktail from the fungus Trichoderma reesei, and thus provides a compelling example of high c
14 porum solani, Alternaria solani, Trichoderma reesei, and Trichoderma harzianum, and an additive antif
15  powerfully cellulolytic fungus, Trichoderma reesei, as an effective CBP microorganism.
16 d with the use of cellulase from Trichoderma reesei at 2 wk after collection.
17 a fusca (E3, E4, and E6) and two Trichoderma reesei (CBH I and CBH II) exocellulases on labeled cello
18   We partially sequenced over 5100 random T. reesei cDNA clones.
19 basis for the lignin affinity of Trichoderma reesei Cel7A carbohydrate binding module (CBM).
20                                           T. reesei Cel7A CBM mutants were produced with a Talaromyce
21 lobiose inhibits the activity of Trichoderma reesei Cel7A, a well-characterized exo-cellulase.
22 ease over the current industrial standard T. reesei Cel7A, and 10% improvement over Aspergillus oryza
23 ynamics of the model fungal CBH, Trichoderma reesei Cel7A.
24 of the cellulolytic model fungus Trichoderma reesei contains two GH7s, termed TrCel7A and TrCel7B.
25 s were detected in the F. graminearum and T. reesei culture samples, respectively, all of which exhib
26 w that cooperator-cheater dynamics within T. reesei/E. coli consortia lead to stable population equil
27 ed a comprehensive mathematical model for T. reesei/E. coli consortia, providing insights on key dete
28  alpha-amylase, the secretion of Trichoderma reesei endoglucanase I (EGI) was not influenced by the Y
29 similar to those for the related Trichoderma reesei exocellulase CBH II.
30 dynamics (MD) simulations of the Trichoderma reesei Family 6 and Family 7 cellobiohydrolases (TrCel6A
31 y by mutating tryptophans in the Trichoderma reesei family 6 cellulase (Cel6A) to alanine.
32          Here, the linker of the Trichoderma reesei Family 7 cellobiohydrolase (Cel7A) is examined by
33 ned on the Family 1 CBM from the Trichoderma reesei Family 7 cellobiohydrolase at three glycosylation
34        The Family 1 CBM from the Trichoderma reesei Family 7 cellobiohydrolase, Cel7A, is known to se
35 comycota) in liquid cultures and assessed T. reesei gene expression relative to each other and relati
36                                      Many T. reesei genes encoding carbohydrate-active enzymes are di
37 ) to generate 34 Mbp of nearly contiguous T. reesei genome sequence comprising 9,129 predicted gene m
38 lase from the microscopic fungus Trichoderma reesei has been shown to give the kinetic parameters K(m
39                               In Trichoderma reesei (Hypocrea jecorina) and Aspergillus niger, we ide
40 y 7 cellobiohydrolase (Cel7A) of Trichoderma reesei (Hypocrea jecorina) was calculated using two diff
41 ndary metabolites may promote survival of T. reesei in its competitive soil habitat, but genome analy
42            Cel7A from the fungus Trichoderma reesei is a model exoglucanase that degrades cellulose s
43                                  Trichoderma reesei is the main industrial source of cellulases and h
44 ess of the carbohydrate-active enzymes of T. reesei, its genome encodes fewer cellulases and hemicell
45 cterization of individual cellulases from T. reesei, like the processive exocellulase Cel7A, shows re
46 eatus Man1 (23.7% identity), and Trichoderma reesei Man1 (22.7% identity).
47  other genera and other cellulases within T. reesei may not be as disordered, warranting further stud
48 ydrolase I (Cel7A) of the fungus Trichoderma reesei (now classified as an anamorph of Hypocrea jecori
49           The filamentous fungus Trichoderma reesei produces and secretes profuse quantities of enzym
50 spergillus niger, A. chevalieri, Trichoderma reesei, Pythium oligandrum, Penicillium sp., and Lasiodi
51 spergillus niger, A. chevalieri, Trichoderma reesei, Pythium oligandrum, Penicillium sp., and Lasiodi
52  single-molecule biophysics) to show that T. reesei Rad51 (TrRad51) is indispensable for interhomolog
53 ungal necromass in situ, we grew Trichoderma reesei RUT-C30 on low and high melanin necromass of Hyal
54 lase preparation from the fungus Trichoderma reesei served as an enzyme source.
55 e GH61 protein into a commercial Trichoderma reesei strain producing high levels of cellulolytic enzy
56 vides a roadmap for constructing enhanced T. reesei strains for industrial applications such as biofu
57 estigation of sexual crossing in Trichoderma reesei, suggesting the possibility of strain improvement
58                                A Trichoderma reesei system expressed A11 with a yield of approximatel
59 canase I (Cel7B) from the fungus Trichoderma reesei that hydrolyzes glycosidic bonds on cellulose ran
60 as some differences from that of Trichoderma reesei; the distinction made between the activities of e
61 dely studied cellulolytic fungus Trichoderma reesei ; thus it can be used to compare cellulases from
62 ezizomycotina filamentous fungus Trichoderma reesei to address if and how Rad51-only eukaryotes condu
63  mobaraensis and tyrosinase from Trichoderma reesei to modify the colloidal properties of protein par
64 ulose by the three main EGs from Trichoderma reesei (Tr): TrCel7B (formerly EG I), TrCel5A (EG II), a
65  like cellobiohydrolase Cel7A of Trichoderma reesei (TrCel7A) are key components of efficient enzyme
66 al Cel7A cellobiohydrolases from Trichoderma reesei (TrCel7A) on the surface of insoluble cellulose f
67         Cellobiohydrolase 1 from Trichoderma reesei (TrCel7A) processively hydrolyses cellulose into
68 reducing-end cellobiohydrolases; Trichoderma reesei (TrCel7A), T. terrestris (TtCel7A), and Mycelioph
69 enzyme formulations derived from Trichoderma reesei, Trichoderma longibrachiatum, Talaromyces emerson
70  CBH TrCel7A and EG TrCel5A from Trichoderma reesei under both single-turnover and "steady state" con
71 tween class II hydrophobins from Trichoderma reesei under different environmental conditions.
72 cellulase cocktails derived from Trichoderma reesei up to 20-fold faster.
73          Transcriptome data revealed that T. reesei up-regulated many genes (over 100; necromass vers
74  The best results were found for Trichoderma reesei using brewers' spent grain (BSG) as substrate.
75 ajor cellulases and xylanases in Trichoderma reesei using the colocation of a fluorescent label (enha
76 III) from the filamentous fungus Trichoderma reesei was investigated by activity, tryptophan fluoresc
77 nase (EC 3.2.1.78 or Man5A) from Trichoderma reesei was investigated by transmission electron microsc
78 se Cel7A from Hypocrea jecorina (Trichoderma reesei), we were able to measure or collect relevant val
79 ween two specialists: the fungus Trichoderma reesei, which secretes cellulase enzymes to hydrolyze li
80 ed a wall hydrolytic enzyme from Trichoderma reesei with potent ability to induce extension of heat-i
81 mary and secondary metabolism of Trichoderma reesei Xpp1 was previously described as a repressor of x