ライフサイエンスコーパス: Penicillium

1 30% sequence identity with thioredoxin from Penicillium.

2 o other eukaryotic organisms, Plasmodium and Penicillium.

3 of allergenic fungi such as Aspergillus and Penicillium.

4 The study of withered grape infection by Penicillium, a potentially toxigenic fungus, is relevant

5 he homologous TqaH and TqaB enzyme pair from Penicillium aethiopicum makes the 2'-epi diastereomer of

6 e is found in the gene cluster identified in Penicillium aethiopicum.

7 lved in viridicatumtoxin (1) biosynthesis in Penicillium aethiopicum.

8 ss of complex indole alkaloids isolated from Penicillium and Aspergillus species.

9 gal extracellular polysaccharides (EPS) from Penicillium and Aspergillus spp., beta-D-glucan, ergoste

10 t benefits and detriments to humans, such as Penicillium and Aspergillus.

11 afine (TRB) and of the echinocandins against Penicillium and Talaromyces species might offer a good t

12 osis (ABPM); other fungi, including Candida, Penicillium, and Curvularia species, are implicated.

13 Contrarily, Penicillium, and Nigrospora were significantly more abun

14 rom 56 isolates of heterologous Aspergillus, Penicillium, and Paecilomyces species or from Neosartory

15 Penicillium arenicola and echinocandin-producing Aspergi

16 irmed that the producing strain NRRL 8095 is Penicillium arenicola and other strains of P. arenicola

17 ication of fungi (especially Aspergillus and Penicillium as proven in this study.

18 related proteins, DAL80 in yeast and NREB in Penicillium, ASD4 does not appear to be involved in regu

19 development of asthma symptoms suggests that Penicillium, Aspergillus, and Cladosporium species pose

20 Exposure to Penicillium, Aspergillus, and Cladosporium species were

21 The results indicated that Cladosporium, Penicillium, Aspergillus, Basidiospores, Epicoccum and P

22 lts were associated with increased levels of Penicillium, Aspergillus, Cladosporium, and Alternaria s

23 eronospora at 30,000 ft; and Alcaligenes and Penicillium at 40,000 ft.

24 fied viral particles from isolate MUT4330 of Penicillium aurantiogriseum var. viridicatum which harbo

25 118 isolates thought to belong to the genus Penicillium based on morphological features were obtaine

26 revianamide A biosynthetic gene cluster from Penicillium brevicompactum NRRL 864 and elucidated the m

27 The filamentous fungus Penicillium brevicompactum produces the immunosuppressiv

28 , which are metabolic products of the fungus Penicillium brevicompactum, are potent agonists at the D

29 , a novel compound isolated from cultures of Penicillium brevicompactum, has been shown to stimulate

30 Chemical investigation of a Penicillium brocae, obtained from a tissue sample of a F

31 nd chlorogriseofulvin, from a marine-derived Penicillium canescens strain.

32 the isolate to be a novel species; the name Penicillium canis sp. nov. is proposed.

33 itive variables on this production enzyme by Penicillium cerradense sp. nov.

34 um halotolerans, Penicillium chrysogenum and Penicillium cf. citrinum were the most frequent species,

35 Saccharomyces cerevisiae (Dal80p and Gzf3p), Penicillium chrysogenum (NREB) and Neurospora crassa (AS

36 vity rates (eg, Cladosporium herbarum 11.1%, Penicillium chrysogenum 10.7%).

37 The properties of Penicillium chrysogenum adenosine 5'-phosphosulfate (APS

38 Cladosporium halotolerans, Penicillium chrysogenum and Penicillium cf. citrinum wer

39 Upon addition of pure Penicillium chrysogenum APS kinase in excess, the overal

40 ethods were applied to biological samples of Penicillium chrysogenum cultivations with different matr

41 d a cell immobilisation system consisting of Penicillium chrysogenum fungi (GRAS) bound to the osmoto

42 Penicillium chrysogenum is a filamentous fungus of major

43 ATP sulfurylase from Penicillium chrysogenum is a homohexameric enzyme that i

44 ATP sulfurylase from Penicillium chrysogenum is an allosteric enzyme in which

45 ATP sulfurylase from Penicillium chrysogenum is an allosterically regulated e

46 Penicillium chrysogenum is the main industrial producer

47 er drought conditions in co-cultivation with Penicillium chrysogenum isolated from Antarctica, Penici

48 ic reprogramming of the antibiotics producer Penicillium chrysogenum toward an industrial pravastatin

49 rt that the CP structure of the fungal dsRNA Penicillium chrysogenum virus (PcV) shows the progenitor

50 ensitisation to Aspergillus fumigatus and/or Penicillium chrysogenum was associated with a lower post

51 d deletion strains of the filamentous fungus Penicillium chrysogenum were used to reassign various pr

52 m, Tausonia pullulans, Naganishia diffluens, Penicillium chrysogenum) as responsible ice-nucleating m

53 obolus but absent in the filamentous fungus, Penicillium chrysogenum, as well as in two nonmethylotro

54 ommon mosquito-associated ascomycete fungus, Penicillium chrysogenum, from the midgut of field-caught

55 m samples taken at a local bakery, including Penicillium chrysogenum, Penicillium citrinum, Cladospor

56 ial chromosome (BIBAC)-based physical map of Penicillium chrysogenum.

57 free APS kinase from the filamentous fungus, Penicillium chrysogenum.

58 free APS kinase from the filamentous fungus, Penicillium chrysogenum.

59 dentity to the P1 zinc-dependent nuclease of Penicillium citrinum (20.8%) and the C-terminal domain o

60 Fusarium kuroshium and Penicillium citrinum were the most dominant fungal assoc

61 Penicillium digitatum, Penicillium italicum, Penicillium citrinum, Aspergillus flavus, Fusarium solan

62 l bakery, including Penicillium chrysogenum, Penicillium citrinum, Cladosporium sphaerospermum, Paeci

63 s were recently successfully used to inhibit Penicillium commune and Mucor racemosus in four dairy pr

64 wo strains of Penicillium expansum (Pe1) and Penicillium crustosum (Pc4).

65 O, Thymus vulgaris L.) on the shelf-life and Penicillium decay of oranges during cold storage.

66 se from Penicillium sp. and naringinase from Penicillium decumbens) previously heated at 70 degrees C

67 ited much higher antifungal activity against Penicillium digitatum and P. italicum, the major pathoge

68 reatment is used in this study to inactivate Penicillium digitatum in lime fruit at post-harvest.

69 e (AS) fruits, leading to resistance against Penicillium digitatum infection.

70 ontrolled recently established infections of Penicillium digitatum on Femminello siracusano lemons bu

71 A Penicillium digitatum strain appeared to be the highest

72 Citrus sinensis (var. Navelina) fruits with Penicillium digitatum was studied at gene expression and

73 nst the most important postharvest pathogen (Penicillium digitatum) of citrus fruit.

74 infection by the following citrus pathogens: Penicillium digitatum, Penicillium italicum, Penicillium

75 The panel included Penicillium digitatum, Penicillium italicum, Rhizopus st

76 days) was associated with resistance against Penicillium digitatum, the main postharvest pathogen of

77 ota of the two alcohol groups, whereas genus Penicillium dominated the mycobiome of nonalcoholic cont

78 rone wine grapes, infected by two strains of Penicillium expansum (Pe1) and Penicillium crustosum (Pc

79 s were effective at inhibiting the growth of Penicillium expansum and Botrytis cinerea, and their eff

80 tissue adjacent to the inoculation sites of Penicillium expansum and Botrytis cinerea.

81 uch as Monilinia spp., Botrytis cinerea, and Penicillium expansum are important fungi that cause post

82 pergillus niger, Aspergillus luchuensis, and Penicillium expansum contamination and postharvest stora

83 ted that extends apple shelf-life by slowing Penicillium expansum growth.

84 rries were inoculated with Botrytis cinerea, Penicillium expansum, Aspergillus niger or A. carbonariu

85 tic pathway were systematically dissected in Penicillium expansum, which is an important fungal patho

86 munesin (cns) biosynthetic gene cluster from Penicillium expansum.

87 Penicillium fellutanum produces a phosphorylated, cholin

88 ibitors of the beta-galactofuranosidase from Penicillium fellutanum.

89 following filtration and Leptospirillium and Penicillium following disinfection.

90 ogenic mycotoxin produced by Aspergillus and Penicillium fungi and so it commonly appears in wines, o

91 ogenic mycotoxin produced by Aspergillus and Penicillium fungi, has been developed and applied for th

92 oduced by several species of Aspergillus and Penicillium fungi.

93 Penicillium (fungi) and Pseudomonadaceae and Enterobacte

94 s with performance comparable or superior to Penicillium funiculosum Cel7A were identified and combin

95 ated from cultures of the filamentous fungus Penicillium funiculosum grown on sugar beet pulp as the

96 ies belonging to four genera of Aspergillus, Penicillium, Fusarium, and Trichoderma with Aspergillus

97 ion through a proof-of-principle analysis of Penicillium genomes and pairwise interaction strength.

98 amentous fungal species (Fusarium oxysporum, Penicillium glabrum).

99 th of Rhizoctonia solani, Phomopsis sp., and Penicillium herguei in media containing a crude protein

100 osynthesis was identified from the genome of Penicillium herquei.

101 Alternaria and Penicillium induced calcium-dependent exocytosis (e.g.,

102 y against Colletotrichum gloeosporioides and Penicillium italicum of jackfruit leaf extracts obtained

103 The fungus Penicillium italicum was found to be the most sensitive

104 was evaluated against the fungal pathogens, Penicillium italicum, Aspergillus niger, Trichoderma har

105 ing citrus pathogens: Penicillium digitatum, Penicillium italicum, Penicillium citrinum, Aspergillus

106 The panel included Penicillium digitatum, Penicillium italicum, Rhizopus stolonifer, Botrytis cine

107 The most abundant was Penicillium jiangxiense in Lot-et-Garonne, known for its

108 Adhesion of Penicillium marneffei conidia to the extracellular matri

109 strated that laminin bound to the surface of Penicillium marneffei conidia.

110 Penicillium marneffei infection is indigenous to Southea

111 Penicillium marneffei is an emerging dimorphic mycosis e

112 Penicillium marneffei is an emerging opportunistic dimor

113 fection with the dimorphic pathogenic fungus Penicillium marneffei is increasingly seen among patient

114 Penicillium marneffei, a dimorphic fungus endemic in par

115 The dimorphic fungus, Penicillium marneffei, is an emerging opportunistic path

116 ides immitis, Paracoccidioides brasiliensis, Penicillium marneffei, Sporothrix schenckii, Cryptococcu

117 LMT system to the emerging pathogenic fungus Penicillium marneffei.

118 atitidis, Paracoccidioides brasiliensis, and Penicillium marneffei.

119 tients and is caused by the dimorphic fungus Penicillium marneffei.

120 apsulatum (histoplasmosis), and Talaromyces (Penicillium) marneffei (talaromycosis).

121 evealed the isolate to be closely related to Penicillium menonorum and Penicillium pimiteouiense.

122 Two diasteroisomers of the Penicillium metabolite penicillenol C1 were synthesized

123 In snow, Cladosporium, Pseudogymnoascus, Penicillium, Meyerozyma, Lecidea, Malassezia, Hanseniasp

124 illium chrysogenum isolated from Antarctica, Penicillium minioluteum isolated from the Atacama Desert

125 The secondary metabolome of Penicillium nordicum is poorly documented despite its fr

126 pase Bs from Saccharomyces cerevisiae (45%), Penicillium notatum (42%), Torulaspora delbrueckii (48%)

127 2 showed strong antifungal activity against Penicillium notatum and P. funiculosum, with an MIC of 4

128 , Rhizopus stolonifer, Aspergillus niger and Penicillium notatum when compared with standards, gentam

129 osporium herbarum, Curvularia spicifera, and Penicillium notatum).

130 tion with exacerbation for indoor culturable Penicillium or total fungi, nitrogen dioxide, rodents (n

131 3; 95% confidence interval (CI), 1.07-3.14], Penicillium [OR = 1.18; (0.98-1.43)], and Cladosporium [

132 sporium [OR = 1.47; (1.16-1.85)]; indoor air Penicillium [OR = 1.26; (0.92-1.74)]; and outdoor air Cl

133 and NJDL-12) were isolated and identified as Penicillium oxalicum and Aspergillus niger respectively

134 gene cluster from the marine-derived fungus Penicillium oxalicum F30 is described along with the cha

135 cal filamentous fungi, Aspergillus niger and Penicillium oxalicum.

136 ncoding 6-methylsalicylic acid synthase from Penicillium patulum was expressed in E. coli and S. cere

137 hylsalicylic acid synthase (6MSAS) gene from Penicillium patulum, to generate plants that constitutiv

138 closely related to Penicillium menonorum and Penicillium pimiteouiense.

139 ngi of the genera Aspergillus, Fusarium, and Penicillium, pose health risks.

140 A greater expression of new Penicillium proteins involved in energy metabolism and s

141 xylan esterase (AXEII; 207 amino acids) from Penicillium purpurogenum has substrate specificities tow

142 An alpha-l-arabinofuranosidase (ABF3) from Penicillium purpurogenum was purified and its possible b

143 ala, Candida, Fusarium, Mucor, Paecilomyces, Penicillium, Rhizopus, Scedosporium, Sporothrix, or othe

144 TUs, including the worldwide reported genera Penicillium, Rhodotorula and Cladosporium.

145 ncentricum, Phanerochaete chrysosporium, and Penicillium rolfsii.

146 Age samples, we observed a high abundance of Penicillium roqueforti and Saccharomyces cerevisiae DNA.

147 Incubation of farnesyl diphosphate (1) with Penicillium roqueforti aristolochene synthase yielded (+

148 Aristolochene synthase (AS) from Penicillium roqueforti catalyzes the cyclization of farn

149 is conserved in aristolochene synthase from Penicillium roqueforti despite the substantial divergent

150 olymer layers and inoculated with the fungus Penicillium roqueforti to provide a living material.

151 olochene synthase from the blue cheese mold, Penicillium roqueforti, is the first of a fungal terpeno

152 Models of Y. lipolytica and K. lactis, with Penicillium roqueforti, were analysed using instrumental

153 Penicillium roquefortii and Aspergillus flavipes present

154 (more than the 90th percentile) of airborne Penicillium (RR = 1.73, 95% confidence interval [CI], 1.

155 e discovery of penicillin, now classified as Penicillium rubens Biourge (1923) (IMI 15378).

156 The most frequent species in our study were Penicillium rubens, P. citrinum, and Talaromyces amestol

157 The fungus Penicillium sclerotiorum produces sclerotiorin, an orang

158 nillyl-alcohol oxidase (VAO) from the fungus Penicillium simplicissimum For oxidation of phenols by V

159 L) were isolated from a DeltaphqK strain of Penicillium simplicissimum, and subsequent enzymatic rea

160 obacter oxydansSphingomonas desiccabilis and Penicillium simplicissimum.

161 tamicibacter arilaitensis (strain JB182) and Penicillium solitum (strain #12).

162 We monitored a population of Penicillium solitum over eight years in a cheese cave an

163 10%) showed high antifungal efficacy against Penicillium sp. and Aspergillus niger but low effective

164 as Aureobasidum pullulans, Phoma macrostoma, Penicillium sp. and Botryotinia fuckeliana, probably ori

165 by alpha-l-rhamnosidases (hesperidinase from Penicillium sp. and naringinase from Penicillium decumbe

166 l genera were Aspergillus sp., Rhizopus sp., Penicillium sp. and Sarocladium sp., occurring at 37, 18

167 e synthesised and exhibited activity against Penicillium sp. Fluorescence and scanning electron micro

168 Results showed that C. gilvescens and Penicillium sp. have potential antibiotic activity again

169 An Australian estuarine isolate of Penicillium sp. MST-MF667 yielded 3 tetrapeptides named

170 udogymnoascus, Cladosporium, Mortierella and Penicillium sp. were the most dominant ASVs detected in

171 ent anthelmintic agent isolated from various Penicillium sp. with promising activity against drug-res

172 gi were detected, including Aspergillus sp., Penicillium sp., and Alternaria sp. Hydrophobic Deep Eut

173 gi were detected, including Aspergillus sp., Penicillium sp., and Alternaria sp. Matrix effect (ME) i

174 tified as Antarctomyces sp., Thelebolus sp., Penicillium sp., and Cryptococcus gilvescens.

175 eri, Trichoderma reesei, Pythium oligandrum, Penicillium sp., and Lasiodiplodia sp. by 60-90%, and de

176 eri, Trichoderma reesei, Pythium oligandrum, Penicillium sp., and Lasiodiplodia sp. by 60-90%, and de

177 a cytotoxic alkaloid isolated from a marine Penicillium sp., belongs to a fascinating family of dens

178 seudogymnoascus roseus, Leotiomycetes sp. 2, Penicillium sp., Mortierella sp. 1, Mortierella sp. 2, P

179 an outbreak investigation of fungemia due to Penicillium species after prolonged flooding of a Thai h

180 Infections caused by Penicillium species are rare in dogs, and the prognosis

181 Penicillium species are some of the most common fungi ob

182 al and genomic findings from Aspergillus and Penicillium species as examples, it is argued that evide

183 ts morphological similarity to nonpathogenic Penicillium species delayed the diagnosis and initiation

184 f Cladosporium, Alternaria, Aspergillus, and Penicillium species increased the exacerbation of curren

185 tilago, Aspergillus, Fusarium, Epichloe, and Penicillium species indicate that oligosaccharide transp

186 associated with clinical disease and 8 were Penicillium species that were not represented in the dat

187 mation included Trichoderma species, whereas Penicillium species was enriched in patients with atopy.

188 Cladosporium, Alternaria, Aspergillus, and Penicillium species were found to be present in higher c

189 frequently cultured in isolation followed by Penicillium species.

190 nent class of indole alkaloids isolated from Penicillium species.

191 istinguish this species from closely related Penicillium species.

192 y metabolite by several fungi species (i.e., Penicillium spp. and Aspergillus spp.).

193 Penicillium spp. are among the major postharvest pathoge

194 Strains of Penicillium spp. are used for fungi-ripened cheeses and

195 id was discovered in Talaromyces stipitatus (Penicillium stipitatum) and investigated by targeted gen

196 e, one diaminopyridine and one derivative of Penicillium stoloniferum in vegetables.

197 The crystal structure of a partitivirus, Penicillium stoloniferum virus F (PsV-F), reveals a diff

198 ted partitiviruses Fusarium poae virus 1 and Penicillium stoloniferum virus F.

199 s were identified within three genera, i.e., Penicillium, Talaromyces, and Rasamsonia The most freque

200 terization of a P450 monooxygenase CnsC from Penicillium that catalyzes the heterodimeric coupling be

201 pora, Austroplaca, Mortierella, Rhodotorula, Penicillium, Thelebolus, Aspergillus, Poaceicola, Glarea

202 of a natural product produced by the fungus Penicillium thymicola.

203 m-Pythium combination had adverse effects on Penicillium, Trichoderma, and Fusarium, and decrease the

204 ile mycelium, were Cladosporium, Alternaria, Penicillium, Ulocadium, Fusarium, Arthrinium, Epicoccum,

205 cies in two fungal genera of Aspergillus and Penicillium under virtually all agricultural environment

206 pergillus ochraceus, Aspergillus unguis, and Penicillium variabile, was significantly associated with

207 nd 20 degrees C), and storage duration on (a)Penicillium verrucosum population, (b)CO(2) respiration

208 ots were inoculated with Botrytis cinerea or Penicillium vulpinum on the day of harvest or after 12,

209 An unknown species of Penicillium was isolated from a bone lesion in a young d

210 Considering composition, Penicillium was the dominant fungal genus, whereas Wolba

211 10 years from 1983 to 1992, Cladosporium and Penicillium were comparable.

212 The genera Cladosporium, Fusarium and Penicillium were the fungi more frequently detected.