ライフサイエンスコーパス: reesei

1 cellobiohydrolase I (CBH I) from Trichoderma reesei.

2 (E212Q) of the enzyme Cel7A from Trichoderma reesei.

3 s, we found and demonstrate (for Trichoderma reesei) alternative, overlapping internal introns.

4 beta-mannanase was isolated from Trichoderma reesei and expressed via the chloroplast genome.

5 gest inhibitory activity against Trichoderma reesei and Pseudomonas solancearum.

6 enzyme cocktail from the fungus Trichoderma reesei, and thus provides a compelling example of high c

7 porum solani, Alternaria solani, Trichoderma reesei, and Trichoderma harzianum, and an additive antif

8 powerfully cellulolytic fungus, Trichoderma reesei, as an effective CBP microorganism.

9 d with the use of cellulase from Trichoderma reesei at 2 wk after collection.

10 a fusca (E3, E4, and E6) and two Trichoderma reesei (CBH I and CBH II) exocellulases on labeled cello

11 We partially sequenced over 5100 random T. reesei cDNA clones.

12 basis for the lignin affinity of Trichoderma reesei Cel7A carbohydrate binding module (CBM).

13 T. reesei Cel7A CBM mutants were produced with a Talaromyce

14 w that cooperator-cheater dynamics within T. reesei/E. coli consortia lead to stable population equil

15 ed a comprehensive mathematical model for T. reesei/E. coli consortia, providing insights on key dete

16 alpha-amylase, the secretion of Trichoderma reesei endoglucanase I (EGI) was not influenced by the Y

17 similar to those for the related Trichoderma reesei exocellulase CBH II.

18 dynamics (MD) simulations of the Trichoderma reesei Family 6 and Family 7 cellobiohydrolases (TrCel6A

19 y by mutating tryptophans in the Trichoderma reesei family 6 cellulase (Cel6A) to alanine.

20 Here, the linker of the Trichoderma reesei Family 7 cellobiohydrolase (Cel7A) is examined by

21 ned on the Family 1 CBM from the Trichoderma reesei Family 7 cellobiohydrolase at three glycosylation

22 The Family 1 CBM from the Trichoderma reesei Family 7 cellobiohydrolase, Cel7A, is known to se

23 Many T. reesei genes encoding carbohydrate-active enzymes are di

24 ) to generate 34 Mbp of nearly contiguous T. reesei genome sequence comprising 9,129 predicted gene m

25 lase from the microscopic fungus Trichoderma reesei has been shown to give the kinetic parameters K(m

26 In Trichoderma reesei (Hypocrea jecorina) and Aspergillus niger, we ide

27 y 7 cellobiohydrolase (Cel7A) of Trichoderma reesei (Hypocrea jecorina) was calculated using two diff

28 ndary metabolites may promote survival of T. reesei in its competitive soil habitat, but genome analy

29 Trichoderma reesei is the main industrial source of cellulases and h

30 ess of the carbohydrate-active enzymes of T. reesei, its genome encodes fewer cellulases and hemicell

31 eatus Man1 (23.7% identity), and Trichoderma reesei Man1 (22.7% identity).

32 other genera and other cellulases within T. reesei may not be as disordered, warranting further stud

33 ydrolase I (Cel7A) of the fungus Trichoderma reesei (now classified as an anamorph of Hypocrea jecori

34 The filamentous fungus Trichoderma reesei produces and secretes profuse quantities of enzym

35 lase preparation from the fungus Trichoderma reesei served as an enzyme source.

36 e GH61 protein into a commercial Trichoderma reesei strain producing high levels of cellulolytic enzy

37 vides a roadmap for constructing enhanced T. reesei strains for industrial applications such as biofu

38 estigation of sexual crossing in Trichoderma reesei, suggesting the possibility of strain improvement

39 A Trichoderma reesei system expressed A11 with a yield of approximatel

40 canase I (Cel7B) from the fungus Trichoderma reesei that hydrolyzes glycosidic bonds on cellulose ran

41 as some differences from that of Trichoderma reesei; the distinction made between the activities of e

42 dely studied cellulolytic fungus Trichoderma reesei ; thus it can be used to compare cellulases from

43 mobaraensis and tyrosinase from Trichoderma reesei to modify the colloidal properties of protein par

44 ulose by the three main EGs from Trichoderma reesei (Tr): TrCel7B (formerly EG I), TrCel5A (EG II), a

45 like cellobiohydrolase Cel7A of Trichoderma reesei (TrCel7A) are key components of efficient enzyme

46 al Cel7A cellobiohydrolases from Trichoderma reesei (TrCel7A) on the surface of insoluble cellulose f

47 Cellobiohydrolase 1 from Trichoderma reesei (TrCel7A) processively hydrolyses cellulose into

48 enzyme formulations derived from Trichoderma reesei, Trichoderma longibrachiatum, Talaromyces emerson

49 CBH TrCel7A and EG TrCel5A from Trichoderma reesei under both single-turnover and "steady state" con

50 III) from the filamentous fungus Trichoderma reesei was investigated by activity, tryptophan fluoresc

51 nase (EC 3.2.1.78 or Man5A) from Trichoderma reesei was investigated by transmission electron microsc

52 se Cel7A from Hypocrea jecorina (Trichoderma reesei), we were able to measure or collect relevant val

53 ween two specialists: the fungus Trichoderma reesei, which secretes cellulase enzymes to hydrolyze li

54 ed a wall hydrolytic enzyme from Trichoderma reesei with potent ability to induce extension of heat-i

55 mary and secondary metabolism of Trichoderma reesei Xpp1 was previously described as a repressor of x