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1 sive cycle of a glycoside hydrolase family 7 cellobiohydrolase.
2 perties of the enzyme indicated that it is a cellobiohydrolase.
3 ms of crystalline cellulose decomposition by cellobiohydrolases.
4 including glycosyl hydrolase family 7 (GH7) cellobiohydrolases.
5 olytic system composed of endoglucanases and cellobiohydrolases.
7 fused domain from the cellulosomal cellulase cellobiohydrolase A (CbhA) of Clostridium thermocellum w
8 st beta-glucosidase, phosphatase, NAGase and cellobiohydrolase activities, and had microbial populati
9 methanesulfonate substrate was used to assay cellobiohydrolase activity on model bacterial strains (E
10 ity toward beta(1,3;1,4)-glucans with a side cellobiohydrolase activity toward beta(1,4)-glucans.
11 can function synergistically with a cognate cellobiohydrolase and endoglucanase to completely releas
12 with which we demonstrate that LqCel7B is a cellobiohydrolase and obtained four high-resolution crys
13 has been mainly attributed to the action of cellobiohydrolases and often linked to the processive me
14 of a highly expressed cellulase (GH6 family cellobiohydrolase) and the CebR transcriptional represso
18 ith polar residues that are conserved in GH7 cellobiohydrolases, but not in GH7 endoglucanases, at th
19 rylase (CbpA), and the apparent absence of a cellobiohydrolase (Cbh) suggest a nonconventional pathwa
20 ct observation shows that chain-end-cleaving cellobiohydrolases (CBH I, CBH II) and an internally cha
21 re-guided recombination of 3 fungal class II cellobiohydrolases (CBH II cellulases) has yielded a col
24 ases (EGs) and chain end-specific processive cellobiohydrolases (CBHs) is that EG-generated new chain
26 biochemical activities of the one annotated cellobiohydrolase Cel6A and the GH5-containing endogluca
27 idues of a glycoside hydrolase (GH) family 6 cellobiohydrolase (Cel6A) and a GH family 7 cellobiohydr
28 A, cel5B, and cel45A) and the sole predicted cellobiohydrolase (cel6A) showed elevated expression dur
30 study of two well characterized enzymes, the cellobiohydrolase Cel7A from Hypocrea jecorina and the c
31 Processive glycoside hydrolases (GHs), like cellobiohydrolase Cel7A of Trichoderma reesei (TrCel7A)
32 ytic domain of Hypocrea jecorina GH Family 7 cellobiohydrolase Cel7A, namely a Michaelis complex with
34 cellobiohydrolase (Cel6A) and a GH family 7 cellobiohydrolase (Cel7A) from the fungus Hypocrea jecor
35 he linker of the Trichoderma reesei Family 7 cellobiohydrolase (Cel7A) is examined by simulation.
36 site of the catalytic tunnel of the Family 7 cellobiohydrolase (Cel7A) of Trichoderma reesei (Hypocre
37 l, multimodular glycoside hydrolase family 7 cellobiohydrolase (Cel7A), which exhibits an O-glycosyla
39 y 1 CBM from the Trichoderma reesei Family 7 cellobiohydrolase, Cel7A, is known to selectively bind t
41 characterized members of a family of fungal cellobiohydrolase class II (CBH II) cellulase chimeras m
42 the one adopted by other cellulases (such as cellobiohydrolases, for example) that frequently contain
43 olases (GH5) and by Cel6A, a nonreducing-end cellobiohydrolase from family GH6 with tandem CBM2s.
44 ity between the family 7 glycoside hydrolase cellobiohydrolases from H. irregulare, H. jecorina, and
45 tly monitor the movement of individual Cel7A cellobiohydrolases from Trichoderma reesei (TrCel7A) on
46 lose crystals acted upon by the exocellulase cellobiohydrolase I (CBH I) from Trichoderma reesei.
48 solution as the mobile phase and the protein cellobiohydrolase I immobilized on silica as the station
50 on, electron microscopy of microfibrils, and cellobiohydrolase I-gold labeling, we report the occurre
53 ssical mechanism involving solubilization by cellobiohydrolase; (ii) bioenergetic benefits specific t
54 strial enzymes, and fungal GH family 7 (GH7) cellobiohydrolases, in particular, provide significant h
55 other cellulolytic systems, thus providing a cellobiohydrolase-independent mechanism for this bacteri
56 the well-characterized Hypocrea jecorina GH7 cellobiohydrolase, LqCel7B exhibits an extended substrat
58 .7 A resolution, confirms that HirCel7A is a cellobiohydrolase rather than an endoglucanase, with a c
59 Identification of the rate-limiting step for cellobiohydrolases remains controversial, and recent rep
60 ionally equivalent to the endoglucanases and cellobiohydrolases required for other cellulolytic syste
61 the Trichoderma reesei Family 6 and Family 7 cellobiohydrolases (TrCel6A and TrCel7A, respectively) b
62 The motion of multiple, individual TrCel7A cellobiohydrolases was simultaneously recorded with appr
63 onstrate that R. albus 8 elaborates multiple cellobiohydrolases with multi-modular architectures that
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