コーパス検索結果 (１語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 sive cycle of a glycoside hydrolase family 7 cellobiohydrolase.
2 perties of the enzyme indicated that it is a cellobiohydrolase.
3 hydrolysis product confirming SMECel6A as a cellobiohydrolase.
4 ms of crystalline cellulose decomposition by cellobiohydrolases.
5 cellobiose inhibition of endoglucanases and cellobiohydrolases.
6 including glycosyl hydrolase family 7 (GH7) cellobiohydrolases.
7 olytic system composed of endoglucanases and cellobiohydrolases.
8 ends are poor attack sites for reducing-end cellobiohydrolases.
9 uence divergence to previously characterised cellobiohydrolases.
10 dizing LPMOs on the activity of reducing-end cellobiohydrolases.
12 fused domain from the cellulosomal cellulase cellobiohydrolase A (CbhA) of Clostridium thermocellum w
13 st beta-glucosidase, phosphatase, NAGase and cellobiohydrolase activities, and had microbial populati
14 methanesulfonate substrate was used to assay cellobiohydrolase activity on model bacterial strains (E
15 ity toward beta(1,3;1,4)-glucans with a side cellobiohydrolase activity toward beta(1,4)-glucans.
16 can function synergistically with a cognate cellobiohydrolase and endoglucanase to completely releas
17 with which we demonstrate that LqCel7B is a cellobiohydrolase and obtained four high-resolution crys
18 s on cellulose chains on the activity of the cellobiohydrolases and found reduced activity against ox
19 has been mainly attributed to the action of cellobiohydrolases and often linked to the processive me
20 tions led to reduced maximal velocity of the cellobiohydrolases and reduced rates of substrate comple
21 The extent of these effects differed for the cellobiohydrolases and scaled with the extent of the imp
22 effect is general for different reducing-end cellobiohydrolases and study the underlying mechanism, w
23 of a highly expressed cellulase (GH6 family cellobiohydrolase) and the CebR transcriptional represso
24 f three His-tagged enzymes beta-glucosidase, cellobiohydrolase, and endoglucanase as well as two prot
28 ith polar residues that are conserved in GH7 cellobiohydrolases, but not in GH7 endoglucanases, at th
29 rylase (CbpA), and the apparent absence of a cellobiohydrolase (Cbh) suggest a nonconventional pathwa
31 beta-glucosidase (BG), beta-xylosidase (BX), cellobiohydrolase (CBH), and their sum associated with C
33 ct observation shows that chain-end-cleaving cellobiohydrolases (CBH I, CBH II) and an internally cha
34 re-guided recombination of 3 fungal class II cellobiohydrolases (CBH II cellulases) has yielded a col
39 ases (EGs) and chain end-specific processive cellobiohydrolases (CBHs) is that EG-generated new chain
40 gineering and screening of processive fungal cellobiohydrolases (CBHs) remain challenging due to limi
41 quantify and track synergistic activity for cellobiohydrolases (CBHs) with a lytic polysaccharide mo
43 biochemical activities of the one annotated cellobiohydrolase Cel6A and the GH5-containing endogluca
44 idues of a glycoside hydrolase (GH) family 6 cellobiohydrolase (Cel6A) and a GH family 7 cellobiohydr
45 A, cel5B, and cel45A) and the sole predicted cellobiohydrolase (cel6A) showed elevated expression dur
47 study of two well characterized enzymes, the cellobiohydrolase Cel7A from Hypocrea jecorina and the c
48 Processive glycoside hydrolases (GHs), like cellobiohydrolase Cel7A of Trichoderma reesei (TrCel7A)
49 ytic domain of Hypocrea jecorina GH Family 7 cellobiohydrolase Cel7A, namely a Michaelis complex with
51 cellobiohydrolase (Cel6A) and a GH family 7 cellobiohydrolase (Cel7A) from the fungus Hypocrea jecor
52 he linker of the Trichoderma reesei Family 7 cellobiohydrolase (Cel7A) is examined by simulation.
53 site of the catalytic tunnel of the Family 7 cellobiohydrolase (Cel7A) of Trichoderma reesei (Hypocre
54 l, multimodular glycoside hydrolase family 7 cellobiohydrolase (Cel7A), which exhibits an O-glycosyla
56 y 1 CBM from the Trichoderma reesei Family 7 cellobiohydrolase, Cel7A, is known to selectively bind t
58 characterized members of a family of fungal cellobiohydrolase class II (CBH II) cellulase chimeras m
59 led similarity to a characterised halophilic cellobiohydrolase despite sharing only 57% sequence iden
61 the one adopted by other cellulases (such as cellobiohydrolases, for example) that frequently contain
62 olases (GH5) and by Cel6A, a nonreducing-end cellobiohydrolase from family GH6 with tandem CBM2s.
63 ity between the family 7 glycoside hydrolase cellobiohydrolases from H. irregulare, H. jecorina, and
64 tly monitor the movement of individual Cel7A cellobiohydrolases from Trichoderma reesei (TrCel7A) on
66 lose crystals acted upon by the exocellulase cellobiohydrolase I (CBH I) from Trichoderma reesei.
68 solution as the mobile phase and the protein cellobiohydrolase I immobilized on silica as the station
70 on, electron microscopy of microfibrils, and cellobiohydrolase I-gold labeling, we report the occurre
73 ssical mechanism involving solubilization by cellobiohydrolase; (ii) bioenergetic benefits specific t
74 strial enzymes, and fungal GH family 7 (GH7) cellobiohydrolases, in particular, provide significant h
75 other cellulolytic systems, thus providing a cellobiohydrolase-independent mechanism for this bacteri
76 the well-characterized Hypocrea jecorina GH7 cellobiohydrolase, LqCel7B exhibits an extended substrat
77 have important implications as reducing-end cellobiohydrolases make up a significant part of such co
79 .7 A resolution, confirms that HirCel7A is a cellobiohydrolase rather than an endoglucanase, with a c
80 Identification of the rate-limiting step for cellobiohydrolases remains controversial, and recent rep
81 ionally equivalent to the endoglucanases and cellobiohydrolases required for other cellulolytic syste
83 the Trichoderma reesei Family 6 and Family 7 cellobiohydrolases (TrCel6A and TrCel7A, respectively) b
84 synergistic effects between the LPMO and the cellobiohydrolases; TrCel7A was severely impeded, TtCel7
85 Thielavia terrestris and three reducing-end cellobiohydrolases; Trichoderma reesei (TrCel7A), T. ter
86 The motion of multiple, individual TrCel7A cellobiohydrolases was simultaneously recorded with appr
87 peding effects varied considerably among the cellobiohydrolases, which may be relevant to consider fo
88 onstrate that R. albus 8 elaborates multiple cellobiohydrolases with multi-modular architectures that