ライフサイエンスコーパス: niger

1 n athletes (from Burkina Faso, Cameroon, and Niger).

2 atory bacterial disease in a Sahel region of Niger.

3 scape for the filamentous fungus Aspergillus niger.

4 ified all mold isolates tested except for A. niger.

5 ty are highly correlated for three cities in Niger.

6 cies recovered, followed by A. flavus and A. niger.

7 r randomized trial of 12 villages in Maradi, Niger.

8 sponse in the filamentous fungus Aspergillus niger.

9 gy to lower the level of PDI in the ER of A. niger.

10 inant gene has been expressed in Aspergillus niger.

11 uringiensis, Bacillus subtilis, and Bacillus niger.

12 active site of glucoamylase from Aspergillus niger.

13 d be applied to the isozyme from Aspergillus niger.

14 were time dependent in batch cultures of A. niger.

15 erases (FAE-III and CinnAE) from Aspergillus niger.

16 temperature-sensitive mutant of Aspergillus niger.

17 that drives colonization of wheat bran in A. niger.

18 opus oligosporus and by >21% for SSF with A. niger.

19 m uncomplicated severe acute malnutrition in Niger.

20 estigate nest construction in the ant Lasius niger.

21 ildren from an antibiotic-naive community in Niger.

22 e case-based meningitis surveillance data in Niger.

23 ngitis cases and 549 deaths were reported in Niger.

24 e rotavirus gastroenteritis among infants in Niger.

25 l gene expression in colonies of Aspergillus niger.

26 glucoamylase from newly isolated Aspergillus niger.

27 ryzae, Aspergillus fumigatus and Aspergillus niger.

28 well as one from the saprotroph Aspergillus niger.

29 Zymes) of the filamentous fungus Aspergillus niger.

30 itis at both national and district levels in Niger.

31 e from 1986 through 2006 for 38 districts in Niger.

32 lysate of the filamentous fungus Aspergillus niger.

33 1.4%), A. flavus (0.8%, 5.1%, and 1.7%), A. niger (17.3%, 3.7%, and 0.6%), A. terreus (0.0%, 1.6%, a

34 /30 min), followed by those from Aspergillus niger (2.4 nmol/1.0 x 10(6) AMs/30 min) and Eurotium ams

35 [7.6-9.7] in Jordan to 51.1% [49.1-53.1] in Niger), 22.7% (22.5-22.9) were underweight (ranging from

36 d in 93% of Aspergillus fumigatus, 75% of A. niger, 25% of A. terreus, and 4% of A. flavus cultures.

37 ed 181 Aspergillus fumigatus, 28 Aspergillus niger, 27 Aspergillus flavus, 22 Aspergillus terreus, se

38 31 to 143 for A. nidulans, 366 to 520 for A. niger, 330 to 462 for A. terreus, and 45 to 84 for A. ve

39 ogram (553 A. fumigatus, 76 A. flavus, 59 A. niger, 35 A. terreus, and 24 A. versicolor isolates and

40 igatus, 235 of A. flavus, 162 of Aspergillus niger, 64 of Aspergillus terreus, and 15 of Aspergillus

41 ved using the free form of inulinase from A. niger (77.19% of GF2; 14.03% of GF3 and 0.07% of GF4) us

42 isk factors in the poorest countries (eg, in Niger, 82% of the population among the poorest billion)

43 ent was observed for isolates of Aspergillus niger (95%), which were particularly susceptible to casp

44 lly, the brain of the Black Skimmer Rynchops niger, a taxon with a unique feeding ecology that involv

45 migatus isolates, and 10 isolates each of A. niger, A. nidulans, and A. terreus to voriconazole, posa

46 es (A. flavus, A. fumigatus, A. nidulans, A. niger, A. terreus, A. ustus, and A. versicolor) was also

47 ates of Aspergillus fumigatus, A. flavus, A. niger, A. terreus, A. ustus, and A. versicolor.

48 solates included A. fumigatus, A. flavus, A. niger, A. terreus, A. versicolor, A. glaucus, A. nidulan

49 Compared with A. niger A1 and L2, A. niger H915-1 contained 92 mutated ge

50 Cebus apella, Saimiri ustius, Saguinus midas niger, Alouatta caraya, Aotus azarae, and Callicebus mol

51 World primates (Cebus apella, Saguinus midas niger, Alouatta caraya, Aotus azarae, and Callicebus mol

52 Aspergillus niger also precipitated lead oxalate during growth in th

53 lead us to conclude that the cofactor in A. niger amine oxidase AO-I has been misidentified.

54 has been reported to exist in an Aspergillus niger amine oxidase AO-I.

55 e of a prolyl endopeptidase from Aspergillus niger (An-PEP) for HDX-MS.

56 was the most common isolate, followed by A. niger and A. flavus.

57 cans, Aspergillus fumigatus, and Aspergillus niger and antibacterial activity against Escherichia col

58 e obtained in Neurospora crassa, Aspergillus niger and Aspergillus awamori by codon optimization of t

59 early indicate that oxalate production in A. niger and B. cinerea is solely dependent on the hydrolyt

60 erium, Bacillus subtilis (including Bacillus niger and Bacillus globigii), Bacillus sphaericus, and B

61 (MAO) was recently isolated from Aspergillus niger and cloned.

62 break response vaccination campaign in urban Niger and compare campaign estimates to measurements fro

63 port identification of tigA from Aspergillus niger and erp38 from Neurospora crassa, two novel member

64 ors of glucose oxidase (GO) from Aspergillus niger and horseradish peroxidase (HRP).

65 FINDINGS: In all pilots except Niger and Madagascar, there were large increases in QAAC

66 herichia coli, Candida albicans, Aspergillus niger and Microsporum gypseum with minimal inhibitory co

67 Both the A. niger and N. crassa proteins show homology with a stress

68 s, and lead oxalate (PbC2O4), produced by A. niger and P. javanicus.

69 Aspergillus niger and Paecilomyces javanicus grew in 5 mM Pb(NO3)2-c

70 Aspergillus niger and Paecilomyces javanicus were grown on modified

71 a albicans, Rhizopus stolonifer, Aspergillus niger and Penicillium notatum when compared with standar

72 nuclear genome of N. tabacum, plastome of H. niger and recombinant mitochondria.

73 nd brandy distillery wastes with Aspergillus niger and Rhizopus oligosporus were investigated.

74 the test manganese oxides after growth of A. niger and S. himantioides at 25 degrees C.

75 Manganese oxides were of low toxicity and A. niger and S. himantioides were able to grow on 0.5% (w/v

76 Aspergillus niger and S. himantioides were capable of solubilizing a

77 The ability of the soil fungi Aspergillus niger and Serpula himantioides to tolerate and solubiliz

78 s of NADPH eukNR from the fungus Aspergillus niger and the (15)epsilon for NADH eukNR from cell homog

79 h (Aspergillus fumigatus, A. flavus, and A. niger), and 48 h (other species); and (iii) the posacona

80 lipsiprymnus), a sable antelope (Hippotragus niger), and a white-tailed deer (Odocoileus virginianus)

81 spp. (64 A. flavus, 391 A. fumigatus, 46 A. niger, and 25 A. terreus isolates) collected from over 6

82 Conditioned media (CM) from A. fumigatus, A. niger, and A. flavus cultures also reduced CBF by ~10% a

83 gillus fumigatus, A. flavus, A. nidulans, A. niger, and A. terreus to caspofungin (MICs and minimum e

84 pecies (Aspergillus fumigatus, A. flavus, A. niger, and A. terreus).

85 ive aspergillosis (IA), with A. nidulans, A. niger, and A. ustus being rare causes of IA.

86 weight in rural areas of Timor-Leste, India, Niger, and Bangladesh.

87 programs in 3 West African countries (Mali, Niger, and Burkina Faso), covering the period 2009-2012.

88 i, P. aeruginosa, S. aureus, C. albicans, A. niger, and S. cerevisiae.

89 untries-Cameroon, Cote d'Ivoire, Madagascar, Niger, and Senegal--collected specimens from patients pr

90 cid-producing fungi, for example Aspergillus niger, and that plants grown with pyromorphite as sole p

91 mmercial enzyme preparation from Aspergillus niger, and the encoding gene was identified.

92 ite Plasmodium vivax, the fungus Aspergillus niger, and the TEM-family of beta-lactamase associated w

93 4 African countries of Burkina Faso, Ghana, Niger, and Uganda.

94 oth experimentally, using colonies of Lasius niger, and with an agent-based simulation model, that ne

95 cose dehydrogenase, derived from Aspergillus niger (AnGDH), was characterized.

96 , however, we show that measles epidemics in Niger are highly episodic, particularly in the capital N

97 lygalacturonase II (EPG-II) from Aspergillus niger as it binds to an oligosaccharide substrate.

98 pergillus (Emericella) nidulans, Aspergillus niger, Aspergillus restrictus, Aspergillus sydowii, Aspe

99 fumigatus, Aspergillus nidulans, Aspergillus niger, Aspergillus terreus, Aspergillus ustus, and Asper

100 s flavus, Aspergillus fumigatus, Aspergillus niger, Aspergillus terreus, Fusarium spp., Pseudallesche

101 s fumigatus, Aspergillus flavus, Aspergillus niger, Aspergillus terreus, Scedosporium prolificans, Sc

102 predict seasonal incidence of meningitis in Niger at both the national and district levels.

103 reak occurred within a single watershed, the Niger basin, rather than between watersheds.

104 geoactive properties, including Aspergillus niger, Beauveria caledonica and Serpula himantioides, we

105 Here, we purified an A. niger beta-glucosidase (AnBgl1) and conducted its bioche

106 In the present work Aspergillus niger beta-glucosidase is immobilized within nanoscale p

107 e was used to capture Bacillus subtilis var. niger (BG) bacterial spores driven to the surface.

108 ydrogen uranyl phosphate were detected on A. niger biomass.

109 uatemala); in some African countries such as Niger, Burundi, and Burkina Faso; and in Vietnam and Chi

110 Trichoderma and Aspergillus niger cellulases activities were determined in a 5 min a

111 OH)2 ) and bioaccumulated within Aspergillus niger colonies when grown on different inorganic nitroge

112 ered cybrids Nicotiana tabacum (+ Hyoscyamus niger) combining the nuclear genome of N. tabacum, plast

113 ulations (Bini and Kanuri Nigerians, who are Niger-Congo [Bantu] and Nilo-Saharan speakers, respectiv

114 rghum population is distributed across early Niger-Congo and Afro-Asiatic language family areas with

115 s associated with the Bantu languages of the Niger-Congo language family, in agreement with the farmi

116 st 7000 years, and that Eastern and Southern Niger-Congo speaking groups share ancestry with Central

117 vity alleles were observed in equatorial and Niger-Congo speaking populations.

118 One involved populations related to Niger-Congo-speaking African populations, and the other

119 e of an over-producing strain of Aspergillus niger containing multiple copies of the encoding aglA ge

120 re, ferulic acid esterase A from Aspergillus niger contributes to total plant cell wall degradation b

121 For infections caused by A. terreus and A. niger, culture and PCR amplification from BAL fluid yiel

122 including those in the areas surrounding the Niger Delta or north western Amazon oil operations; thos

123 torial Atlantic (EEA) sediment core from the Niger Delta.

124 alpha-casein (alphas-CN) with an Aspergillus niger derived prolyl endoproteinase (An-PEP) for 1, 2, 3

125 specific endoglucanase (CEG from Aspergillus niger) did not cause cell wall creep, either by itself o

126 The crystal structure of A. niger DMML (in complex with Mg(2+) and in complex with M

127 Lower Cretaceous fossils from central Niger document the succession of sauropod dinosaurs on A

128 This and the finding that A. niger does not thrive on nicotinamide as a sole carbon s

129 Lead oxalate was precipitated by Aspergillus niger during bioleaching of natural and synthetic vanadi

130 me PGC is produced by the fungus Aspergillus niger during invasion of plant cell walls.

131 e production of lead oxalate dihydrate by A. niger during pyromorphite transformation, which is the f

132 consists of glucose oxidase from Aspergillus niger electrically "wired" by polymer I, having a redox

133 Finally, our results demonstrate that A. niger employs different enzymatic tools to adapt its met

134 of the eroA and ervA genes from Aspergillus niger, encoding functional orthologues of S. cerevisiae

135 chia coli expressing recombinant Aspergillus niger epoxide hydrolase as the model enzyme for various

136 In contrast to Ero1p in S. cerevisiae, A. niger EroA appears to be retained in the ER lumen by a C

137 ts show that the specificities of the two A. niger esterases are complementary.

138 Using Aspergillus niger Fdc1 as a model system, we reveal that isomerizati

139 from a community-based cohort of children in Niger followed from August 2006 to March 2007.

140 ampled in four regions of Senegal, Mali, and Niger from 1983-2012, using satellite-derived vegetation

141 e Arabidopsis thaliana plant and Aspergillus niger fungal species are presented.

142 The Aspergillus niger genome contains four genes that encode proteins ex

143 BLAST analysis of the A. niger genome for the presence of a similar pathway revea

144 ns assays were conducted against Aspergillus niger given its strong resistance and its relevance in s

145 e starch-binding domain (SBD) of Aspergillus niger glucoamylase 1 (GA-I) with substrate has been inve

146 and bread improver, similarly to Aspergillus niger glucose oxidase (GOX).

147 ological samples, the culture filtrate of A. niger grown on wheat straw.

148 V-1-infected people in Ivory Coast, Nigeria, Niger, Guinea Bissau, Benin, and Equatorial Guinea.

149 ysis of citrate-producing strains-namely, A. niger H915-1 (citrate titer: 157 g L(-1)), A1 (117 g L(-

150 Compared with A. niger A1 and L2, A. niger H915-1 contained 92 mutated genes, including a suc

151 Furthermore, transcriptome analysis of A. niger H915-1 revealed that the transcription levels of 4

152 The 2012 Countdown profile shows that Niger has achieved far greater reductions in child morta

153 ain (SBD) of glucoamylase 1 from Aspergillus niger has been determined by heteronuclear multidimensio

154 e inotocin from the black garden ant (Lasius niger), identified and cloned its cognate receptor and d

155 omyces marxianus NRRL Y 7571 and Aspergillus niger in an aqueous-organic system.

156 first used widely in Burkina Faso, Mali, and Niger in December 2010 with great success.

157 ne was introduced in Burkina Faso, Mali, and Niger in December 2010.

158 n x-ray structures of a PME from Aspergillus niger in deglycosylated and Asn-linked N-acetylglucosami

159 tion of heterologous proteins in Aspergillus niger include the manipulation of chaperones and foldase

160 Aspergillus niger is known to secrete large amounts of beta-glucosid

161 n-linked sulfhydryl oxidase from Aspergillus niger is related to the pyridine nucleotide-dependent di

162 zole, 1 (97.7%); voriconazole, 2 (99.3%); A. niger, itraconazole, 2 (100%); posaconazole, 0.5 (96.9%)

163 y of African Americans is predominantly from Niger-Kordofanian (approximately 71%), European (approxi

164 frican ancestry is most similar to non-Bantu Niger-Kordofanian-speaking populations, consistent with

165 ungal protein expression system (Aspergillus niger) leads to significantly enhanced specific growth r

166 Monoamine oxidase from Aspergillus niger (MAO-N) is a flavoenzyme that catalyses the oxidat

167 monoamine oxidase variants from Aspergillus niger (MAO-N) which display remarkable substrate scope a

168 atic (endopolygalacturonase from Aspergillus niger) methods.

169 n vaccination campaigns was collected by the Niger Ministry of Health and WHO.

170 estores oxalate production in an Aspergillus niger mutant strain, lacking a functional oahA gene.

171 The present work showed that A. niger NaR lost 99.2% of soluble activity on vacuum-dryin

172 kina Faso, Chad, Cote d'Ivoire, Ghana, Mali, Niger, Nigeria, and Togo) collected and curated by the W

173 ublic of the Congo, Ethiopia, Guinea, Kenya, Niger, Nigeria, Sierra Leone, and Uganda.

174 public of Congo, Ghana, Cote d'Ivoire, Mali, Niger, Nigeria, Togo).

175 subsidised ACTs in Ghana, Kenya, Madagascar, Niger, Nigeria, Uganda, and Tanzania (including Zanzibar

176 DNA array analysis showed that unlike the A. niger oah gene, the DMML encoding gene is subject to cat

177 ative top predator, the chain pickerel (Esox niger), on contemporary timescales.

178 m A. candidus, whereas spores from either A. niger or E. amstelodami activated p56(Hck), p72(Syk), an

179 inetic constants of starch hydrolysis for A. niger parent and mutant GAs calculated on the basis of m

180 e three-dimensional structure of Aspergillus niger pectin lyase B (PLB) has been determined by crysta

181 evant recombinant glycoproteins (Aspergillus niger phytase and anti-HIV antibody 2G12) produced in di

182 lding of the protein; and a heat-resistant A.niger phytase may be achieved by mutating certain critic

183 Aspergillus niger phytase shares 66% sequence identity, however, it

184 of either the expression of the Aspergillus niger polygalacturonase II (AnPGII; 35S:AnPGII plants) o

185 entity with glucose oxidase from Aspergillus niger, possesses an amino-terminal sequence homologous t

186 a-rhamnosidase from a commercial Aspergillus niger preparation, were immobilized onto acrylic beads.

187 However, Malcosteus niger produces far-red bioluminescence and its longwave

188 The hydrolytic specificity of Aspergillus niger prolyl endoproteinase (An-PEP) on purified beta-ca

189 upplementation with enzymes like Aspergillus niger propyl-endoprotease (AN-PEP), which can hydrolyse

190 e Upper Permian Moradi Formation of northern Niger provide an insight into the faunas that inhabited

191 ptian) rocks in the Tenere Desert of central Niger provide new information about spinosaurids, a pecu

192 Cdc42, Rac1 and Rho function in Aspergillus niger provides the first global perspective on their res

193 tion and degradation of wheat bran by the A. niger reference strain CBS 137562 and araR/xlnR regulato

194 e, ferulic acid esterase A, from Aspergillus niger releases ferulic acid and 5-5- and 8-O-4-dehydrodi

195 fied as Penicillium oxalicum and Aspergillus niger respectively in this study.

196 m has a restricted distribution by the upper Niger River and its tributaries that is associated with

197 as domesticated in a single region along the Niger river as opposed to noncentric domestication event

198 gar, in conjunction with urea hydrolysis and Niger seed agar, or D2 LSU sequencing can be reliably us

199 We report the first meningitis epidemic in Niger since the nationwide introduction of MACV.

200 Aspergillus tubingensis, a member of the A. niger species complex, is described from clinical specim

201 erichia coli O157:H7, Bacillus subtilis var. niger spores, and Staphylococcal enterotoxin type B from

202 Previous studies have shown that a mutant A. niger strain lacking the OAH gene does not produce oxala

203 We report a pseudo-outbreak of Aspergillus niger that followed building construction in our clinica

204 ed a candidate fungal extract of Aspergillus niger that inhibited the interaction between FREP1 and P

205 en in rural areas of Burundi, Guatemala, and Niger the shortest, with the tallest and shortest more t

206 history of citrate production in Aspergillus niger, the molecular mechanism of citrate accumulation i

207 ke the native OxDC isolated from Aspergillus niger, the recombinant, bacterial OxDC from Bacillus sub

208 In Aspergillus niger, the target protein is normally fused downstream o

209 decentralised nutrition programmes permitted Niger to decrease child mortality at a pace that exceeds

210 Countdown therefore invited Niger to do an in-depth analysis of their child survival

211 ed a randomized, placebo-controlled trial in Niger to evaluate the efficacy of a live, oral bovine ro

212 y 1, 2003, and December 31, 2010, in Niamey, Niger, to determine risk factors for bacterial meningiti

213 pathogens, Penicillium italicum, Aspergillus niger, Trichoderma harzianum and Botrytis cinerea.

214 In A. niger, two transcription factors, AraR and XlnR, regulat

215 of glaA was attenuated in that strain of A. niger, UPR was not evident, suggesting that the transcri

216 of ferulic acid esterase A from Aspergillus niger using a range of synthetic ethyl esterified dehydr

217 as observed, but binding to A. flavus and A. niger was calcium dependent.

218 kotanin biosynthetic pathway of Aspergillus niger was expressed in Saccharomyces cerevisiae.

219 The phytase gene from Aspergillus niger was inserted into soybean transformation plasmids

220 dren aged 1-60 months in the Dosso region of Niger was randomized to receive a single dose of either

221 ocess, and beta-glucosidase from Aspergillus niger was selected.

222 a reesei (Hypocrea jecorina) and Aspergillus niger, we identified the genes lxr4 and xhrA, respective

223 a double-blind, placebo-controlled trial in Niger, we randomly assigned children who were 6 to 59 mo

224 r fungal pigments extracted from Aspergillus niger were analyzed by MALDI-TOF and MALDI-qTOF (quadrup

225 t and hyphal negative control extracts of A. niger were not inhibited.

226 cterial endospores of Bacillus subtilis var. niger were obtained in a bipolar aerosol time-of-flight

227 ant mutant of a locally isolated Aspergillus niger were purified to apparent homogeneity.

228 ioral audiograms of 2 fox squirrels (Sciurus niger) were determined with a conditioned avoidance proc

229 atrophaeus, formerly Bacillus subtilis var. niger, were analyzed using bioaerosol mass spectrometry.

230 Forty-eight communities in Matameye, Niger, were randomized to annual oral azithromycin treat

231 ctase glucose oxidase (GOx) from Aspergillus niger, which is the most frequently applied enzyme in el

232 rage of four heterogeneous countries: Nepal, Niger, Yemen, and Zambia.

233 ering FOS synthesis using the enzyme from A. niger, yields of 26.62% of GF2 (kestose), 30.62% of GF3