ライフサイエンスコーパス: Trichoderma reesei

1 by filamentous fungi (hydrophobin HFBI from Trichoderma reesei).

2 xocellulase cellobiohydrolase I (CBH I) from Trichoderma reesei.

3 th in the industrial enzyme-producing fungus Trichoderma reesei.

4 AA9A of the cellulose-degrading model fungus Trichoderma reesei.

5 e filamentous fungi Fusarium graminearum and Trichoderma reesei.

6 ent variant (E212Q) of the enzyme Cel7A from Trichoderma reesei.

7 In others, we found and demonstrate (for Trichoderma reesei) alternative, overlapping internal in

8 ne encoding beta-mannanase was isolated from Trichoderma reesei and expressed via the chloroplast gen

9 on of two fungal family AA9 LPMOs, TrAA9A of Trichoderma reesei and NcAA9C of Neurospora crassa, and

10 ed the strongest inhibitory activity against Trichoderma reesei and Pseudomonas solancearum.

11 subset of 57 GH7 CBH genes was expressed in Trichoderma reesei and screened using a multiplexed acti

12 cellulolytic enzyme cocktail from the fungus Trichoderma reesei, and thus provides a compelling examp

13 usarium oxysporum solani, Alternaria solani, Trichoderma reesei, and Trichoderma harzianum, and an ad

14 veloping the powerfully cellulolytic fungus, Trichoderma reesei, as an effective CBP microorganism.

15 rritin method with the use of cellulase from Trichoderma reesei at 2 wk after collection.

16 ermomonospora fusca (E3, E4, and E6) and two Trichoderma reesei (CBH I and CBH II) exocellulases on l

17 structural basis for the lignin affinity of Trichoderma reesei Cel7A carbohydrate binding module (CB

18 by which cellobiose inhibits the activity of Trichoderma reesei Cel7A, a well-characterized exo-cellu

19 molecular dynamics of the model fungal CBH, Trichoderma reesei Cel7A.

20 e secretome of the cellulolytic model fungus Trichoderma reesei contains two GH7s, termed TrCel7A and

21 Unlike rice alpha-amylase, the secretion of Trichoderma reesei endoglucanase I (EGI) was not influen

22 results are similar to those for the related Trichoderma reesei exocellulase CBH II.

23 d molecular dynamics (MD) simulations of the Trichoderma reesei Family 6 and Family 7 cellobiohydrola

24 g free energy by mutating tryptophans in the Trichoderma reesei family 6 cellulase (Cel6A) to alanine

25 Here, the linker of the Trichoderma reesei Family 7 cellobiohydrolase (Cel7A) is

26 on are examined on the Family 1 CBM from the Trichoderma reesei Family 7 cellobiohydrolase at three g

27 The Family 1 CBM from the Trichoderma reesei Family 7 cellobiohydrolase, Cel7A, is

28 rified cellulase from the microscopic fungus Trichoderma reesei has been shown to give the kinetic pa

29 In Trichoderma reesei (Hypocrea jecorina) and Aspergillus n

30 of the Family 7 cellobiohydrolase (Cel7A) of Trichoderma reesei (Hypocrea jecorina) was calculated us

31 Cel7A from the fungus Trichoderma reesei is a model exoglucanase that degrades

32 Trichoderma reesei is the main industrial source of cell

33 rgillus aculeatus Man1 (23.7% identity), and Trichoderma reesei Man1 (22.7% identity).

34 Cellobiohydrolase I (Cel7A) of the fungus Trichoderma reesei (now classified as an anamorph of Hyp

35 The filamentous fungus Trichoderma reesei produces and secretes profuse quantit

36 growth of Aspergillus niger, A. chevalieri, Trichoderma reesei, Pythium oligandrum, Penicillium sp.,

37 growth of Aspergillus niger, A. chevalieri, Trichoderma reesei, Pythium oligandrum, Penicillium sp.,

38 n decaying fungal necromass in situ, we grew Trichoderma reesei RUT-C30 on low and high melanin necro

39 crude" cellulase preparation from the fungus Trichoderma reesei served as an enzyme source.

40 gene for one GH61 protein into a commercial Trichoderma reesei strain producing high levels of cellu

41 ilitated investigation of sexual crossing in Trichoderma reesei, suggesting the possibility of strain

42 A Trichoderma reesei system expressed A11 with a yield of

43 s on endoglucanase I (Cel7B) from the fungus Trichoderma reesei that hydrolyzes glycosidic bonds on c

44 ase system has some differences from that of Trichoderma reesei; the distinction made between the act

45 nt of the widely studied cellulolytic fungus Trichoderma reesei ; thus it can be used to compare cell

46 e used the Pezizomycotina filamentous fungus Trichoderma reesei to address if and how Rad51-only euka

47 Streptomyces mobaraensis and tyrosinase from Trichoderma reesei to modify the colloidal properties of

48 soluble cellulose by the three main EGs from Trichoderma reesei (Tr): TrCel7B (formerly EG I), TrCel5

49 lases (GHs), like cellobiohydrolase Cel7A of Trichoderma reesei (TrCel7A) are key components of effic

50 of individual Cel7A cellobiohydrolases from Trichoderma reesei (TrCel7A) on the surface of insoluble

51 Cellobiohydrolase 1 from Trichoderma reesei (TrCel7A) processively hydrolyses cel

52 s and three reducing-end cellobiohydrolases; Trichoderma reesei (TrCel7A), T. terrestris (TtCel7A), a

53 Using model enzyme formulations derived from Trichoderma reesei, Trichoderma longibrachiatum, Talarom

54 lose (BC) by CBH TrCel7A and EG TrCel5A from Trichoderma reesei under both single-turnover and "stead

55 on forces between class II hydrophobins from Trichoderma reesei under different environmental conditi

56 ocessed via cellulase cocktails derived from Trichoderma reesei up to 20-fold faster.

57 The best results were found for Trichoderma reesei using brewers' spent grain (BSG) as s

58 ibution of major cellulases and xylanases in Trichoderma reesei using the colocation of a fluorescent

59 lucanase (EGIII) from the filamentous fungus Trichoderma reesei was investigated by activity, tryptop

60 a beta-mannanase (EC 3.2.1.78 or Man5A) from Trichoderma reesei was investigated by transmission elec

61 lobiohydrolase Cel7A from Hypocrea jecorina (Trichoderma reesei), we were able to measure or collect

62 divided between two specialists: the fungus Trichoderma reesei, which secretes cellulase enzymes to

63 ave identified a wall hydrolytic enzyme from Trichoderma reesei with potent ability to induce extensi

64 of both primary and secondary metabolism of Trichoderma reesei Xpp1 was previously described as a re