ライフサイエンスコーパス: Trichoderma

1 commercial preparations from Aspergillus and Trichoderma.

2 Products containing Trichoderma, Ampelomyces quisqualis, Bacillus, and Ulocl

3 Trichoderma and Aspergillus niger cellulases activities

4 inearum affected fungal endophytes including Trichoderma and Endogone.

5 vern the recognition and association between Trichoderma and their hosts are still largely unknown.

6 mutualists, including Pseudomonas, Bacillus, Trichoderma, and mycorrhiza species sensitize the plant

7 Trichoderma arundinaceum (Ta37) and Botrytis cinerea (B0

8 s a non-phytotoxic trichothecene produced by Trichoderma arundinaceum.

9 nsortium of arbuscular mycorrhizal fungi and Trichoderma atroviride (coated and uncoated seeds during

10 oned from strain P1 of the biocontrol fungus Trichoderma atroviride (formerly T. harzianum).

11 The protein EPL1 from the fungus Trichoderma atroviride belongs to the cerato-platanin pr

12 , Hypocrea atroviride (the telomorph form of Trichoderma atroviride) secretes an Sm1-homologous prote

13 , we describe that in the filamentous fungus Trichoderma atroviride, injury results in the formation

14 nge of fungi, including the biocontrol agent Trichoderma atroviride, the plant pathogens Fusarium gra

15 of four foliar endophytes (Stachybotrys sp., Trichoderma atroviride, Ulocladium atrum or Truncatella

16 s complex (15%), the newly described species Trichoderma bissettii (12%), and Trichoderma orientale (

17 the wide range of mechanisms involved we use Trichoderma/Botrytis as an exemplar system.

18 e (Suc) is an important resource provided to Trichoderma cells and is also associated with the contro

19 ichoderma longibrachiatum (26%), followed by Trichoderma citrinoviride (18%), the Hypocrea lixii/Tric

20 licate populations of the filamentous fungus Trichoderma citrinoviride underwent 85 serial transfers,

21 Fungal species belonging to the genus Trichoderma colonize the rhizosphere of many plants, res

22 red with that of a commercial preparation of Trichoderma endo-glucanase (EndoGase).

23 luded lysozyme, zymolyase, and Cytophaga and Trichoderma extracts and was seen to reduce contaminatio

24 mily 10, 62 and anarabinofuranosidase of the Trichoderma genus and Xyl2 contained a protein with simi

25 ns, Penicillium italicum, Aspergillus niger, Trichoderma harzianum and Botrytis cinerea.

26 enzymes secreted by the mycoparasitic fungi Trichoderma harzianum and Trichoderma virens.

27 Expression of tri5 in the biocontrol strain Trichoderma harzianum CECT 2413 resulted in production o

28 xt, recombinant endo-beta-1,6-glucanase from Trichoderma harzianum is utilized to release all the bet

29 Root colonization with Trichoderma harzianum Rifai strain 22 (T22) induces larg

30 erma citrinoviride (18%), the Hypocrea lixii/Trichoderma harzianum species complex (15%), the newly d

31 , Alternaria solani, Trichoderma reesei, and Trichoderma harzianum, and an additive antifungal effect

32 the application of endophytic fungi, such as Trichoderma harzianum, that act as biocontrol agents by

33 d resistance, respectively, conferred by the Trichoderma inoculation.

34 A set of 73 isolates of the emerging fungus Trichoderma isolated from human and animal clinical spec

35 The most frequent species was Trichoderma longibrachiatum (26%), followed by Trichoder

36 ed Fusarium oxysporum f. sp. lycopersici and Trichoderma longibrachiatum hyphal growth in vitro, alth

37 Trichoderma longibrachiatum infection of the skin in an

38 m sp. isolates, 23 dematiaceous fungi, and 5 Trichoderma longibrachiatum isolates).

39 regarding the identification of molds in the Trichoderma longibrachiatum species aggregate are presen

40 Trichoderma longibrachiatum was recovered from stool sur

41 lomyces lilacinus, Scedosporium prolificans, Trichoderma longibrachiatum, and Wangiella dermatitidis

42 ormulations derived from Trichoderma reesei, Trichoderma longibrachiatum, Talaromyces emersonii and r

43 Cultures were positive for Trichoderma longibrachiatum.

44 bed species Trichoderma bissettii (12%), and Trichoderma orientale (11%).

45 t the elicitor's aggregation may control the Trichoderma-plant molecular dialogue and block the activ

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

47 In Trichoderma reesei (Hypocrea jecorina) and Aspergillus n

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

67 Trichoderma reesei is the main industrial source of cell

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

69 The filamentous fungus Trichoderma reesei produces and secretes profuse quantit

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

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

72 A Trichoderma reesei system expressed A11 with a yield of

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

91 necessary for the up-regulation of Sm1, the Trichoderma-secreted elicitor that systemically activate

92 Trichoderma species are efficient mycoparasites and prol

93 Trichoderma species are widely used in agriculture and i

94 While Trichoderma species have been recognized to be pathogeni

95 t colonization by Bacillus, Clavibacter, and Trichoderma species, a list likely to grow as knowledge

96 Trichoderma spp. are effective biocontrol agents for sev

97 A review of the literature suggests that Trichoderma spp. are recognized as human pathogens with

98 ntrol, including the generation of optimized Trichoderma strains against M. roreri, new biopesticides

99 niothyrium minitans, species of Gliocladium, Trichoderma, Streptomyces, and Bacillus, and nonpathogen

100 he same levels of systemic protection as non-Trichoderma-treated plants.

101 de of effect on rust severity, Stachybotrys, Trichoderma, Ulocladium and Truncatella were ranked in t

102 erization of an intracellular invertase from Trichoderma virens (TvInv) important for the mechanisms

103 The fungus Trichoderma virens is a ubiquitous soil saprophyte that

104 The soilborne fungus Trichoderma virens secretes a small protein (Sm1) that i

105 shown that the beneficial filamentous fungus Trichoderma virens secretes the highly effective hydroph

106 cterization of one such HRPKS (Tv6-931) from Trichoderma virens showed that the cAT domain is capable

107 ycoparasitic fungi Trichoderma harzianum and Trichoderma virens.

108 An ethylene-inducing xylanase (Eix) of Trichoderma viride is a potent elicitor of plant defense

109 The effect of xylanase type (Trichoderma viride or Neocallimastix patriciarum) and gr

110 sence and absence of the antagonistic fungus Trichoderma viride, a biological control agent that has

111 mong three distinct family 5 cellulases from Trichoderma viride, Thermogata maritima, and Pyrococcus

112 on, numerous proteins induced in response to Trichoderma were those involved in stress and defense re

113 s as a signalling VOC in the interactions of Trichoderma with plants and other microorganisms by modu