ライフサイエンスコーパス: Trichoderma

1 y in combination of biological control using Trichoderma.

2 d avoidance of enhanced root colonization by Trichoderma.

3 RNA-MGS pathways during its interaction with Trichoderma.

4 phytophthora blight disease with and without Trichoderma.

5 elated genes, and (iii) root colonization by Trichoderma.

6 to establish a beneficial relationship with Trichoderma.

7 response that mirrors their response to live Trichoderma.

8 commercial preparations from Aspergillus and Trichoderma.

9 Tomato plants colonized by the soil fungus Trichoderma afroharzianum, a beneficial microorganism wi

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

11 Trichoderma and Aspergillus niger cellulases activities

12 ominant species were Stachybotrys, Fusarium, Trichoderma and Cochlonema.

13 inearum affected fungal endophytes including Trichoderma and Endogone.

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

15 bination had adverse effects on Penicillium, Trichoderma, and Fusarium, and decrease the overall alph

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

17 Our environmental data showed that Trichoderma are the most abundant noncultivar fungi in w

18 Trichoderma arundinaceum (Ta37) and Botrytis cinerea (B0

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

20 derived from the As-resistant fungal strain Trichoderma asperellum SM-12F1, mitigates As(III) and MA

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

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

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

24 Trichoderma atroviride is a root-colonizing fungus that

25 absence of histone deacetylase HDA-2 in the Trichoderma atroviride strain Deltahda-2 impacts its eff

26 e a functional clock in the biocontrol agent Trichoderma atroviride to assess its importance in the m

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

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

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

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

31 will be beneficial for developing efficient Trichoderma-based biocontrol agents.

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

33 d of herbivory, MIR, especially triggered by Trichoderma, boosted green leaf volatile emissions, enha

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

35 , 60 isolates were identified as 11 species: Trichoderma brevicompactum, species in Harzianum clade i

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

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

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

39 psis, Volutella, Cladosporium, Stachybotrys, Trichoderma, Cochlonema and two unknown fungal species)

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

41 Additionally, plant growth induced by Trichoderma depends on functional RdDM.

42 se incidence ratings than the control, while Trichoderma did not show beneficial effects on controlli

43 There are fewer studies on Trichoderma diversity in agricultural fields.

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

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

46 statistical prioritization of metabolites in Trichoderma extracts demonstrated that T. septentrionali

47 econdary metabolites known to be produced by Trichoderma fungi.

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

49 sources are limited, the hypocrealean fungus Trichoderma guizhouense can overgrow another hypocrealea

50 Using Trichoderma guizhouense NJAU4742 and magnetite (Mt) as a

51 f a GH1 beta-glucosidase highly expressed by Trichoderma harzianum (ThBgl) under biomass degradation

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

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

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

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

56 ent research, a maize straw biochar (MB) and Trichoderma harzianum loaded biochar (MBT) were used at

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

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

59 Focusing on the biofertilizer Trichoderma harzianum t-22, we identified and characteri

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

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

62 SA- and JA-related genes were primed by Trichoderma in leaves after the application of the well-

63 ther determined that metabolites produced by Trichoderma induce an ant weeding response that mirrors

64 In vitro results showed that Trichoderma inhibited P. capsici growth while biochar di

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

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

67 The potential use of these African Trichoderma isolates in classical biological control, ei

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

69 y evaluated TLX, a xylanase preparation from Trichoderma longibrachiatum (TLX), with xylan-rich foods

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

71 Trichoderma longibrachiatum infection of the skin in an

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

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

74 Trichoderma longibrachiatum was recovered from stool sur

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

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

77 Cultures were positive for Trichoderma longibrachiatum.

78 A survey for species of the genus Trichoderma occurring as endophytes of Coffea, and as my

79 rence and high abundance of the fungal genus Trichoderma on decaying fungal necromass in situ, we gre

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

81 port that peptaibols act as chemical cues of Trichoderma pathogenesis in T. septentrionalis fungus ga

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

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

84 In Trichoderma reesei (Hypocrea jecorina) and Aspergillus n

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

111 Trichoderma reesei is the main industrial source of cell

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

113 The filamentous fungus Trichoderma reesei produces and secretes profuse quantit

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

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

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

117 A Trichoderma reesei system expressed A11 with a yield of

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

143 e filamentous fungi Fusarium graminearum and Trichoderma reesei.

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

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

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

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

148 otein-4 (NSP4) locus, which is responsive to Trichoderma, showed altered epigenetic modifications in

149 es, with the two most abundant species being Trichoderma sp. and Pichia guilliermondi.

150 Trichoderma species are efficient mycoparasites and prol

151 Trichoderma species are widely used in agriculture and i

152 reveal a previously unrecorded diversity of Trichoderma species endophytic in both wild and cultivat

153 While Trichoderma species have been recognized to be pathogeni

154 The rhizosphere of 16 crops was analyzed for Trichoderma species in 7 districts of Rajasthan state of

155 c properties, and geographic distribution of Trichoderma species will be beneficial for developing ef

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

157 patients with T2-high inflammation included Trichoderma species, whereas Penicillium species was enr

158 ro-residues by direct fermentation using two Trichoderma species.

159 iciting fungi: an arbuscular mycorrhizal and Trichoderma species; and the tri-trophic system includin

160 All patients with Trichoderma spp fungemia were exposed to corticosteroids

161 the second most frequent (10%), followed by Trichoderma spp, Aspergillus spp, and Mucorales (5% each

162 Trichoderma spp. are a rich source of secondary metaboli

163 Trichoderma spp. are effective biocontrol agents for sev

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

165 tory infection experiments to establish that Trichoderma spp. can act as previously unrecognized path

166 athogenesis in humans and in animals and for Trichoderma spp. symbiotic and antagonistic behavior.

167 Upon interaction with Trichoderma, sRNA-MGS-related genes paralleled the expre

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

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

170 importance of HDA-2 as a global regulator in Trichoderma to modulate multiple responses in Arabidopsi

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

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

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

174 f maize (Zea mays) and the beneficial fungus Trichoderma virens and identified 12-oxo-phytodienoic ac

175 The fungus Trichoderma virens is a ubiquitous soil saprophyte that

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

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

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

179 ycoparasitic fungi Trichoderma harzianum and Trichoderma virens.

180 of this approach using tomato recognition of Trichoderma viride ethylene-inducing xylanase (EIX) as a

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

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

183 or copper ions) or chemical and biological (Trichoderma viride) agents on plant secondary metabolite

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

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

186 ilian states, suggesting the existence of a 'Trichoderma void' in the endophyte mycobiota of coffee o

187 In sharp contrast, not a single isolate of Trichoderma was obtained using the same isolation protoc

188 Trichoderma was the most abundant genus recovered from a

189 Ninety-four isolates of Trichoderma were obtained during this study: 76 as endop

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

191 a of Aspergillus, Penicillium, Fusarium, and Trichoderma with Aspergillus as the predominant genus we

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

193 biochar (different biochar treatments), and Trichoderma (without or with inoculation).