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1 ia coli could be applied to the isozyme from Aspergillus niger.
2 e of two esterases (FAE-III and CinnAE) from Aspergillus niger.
3  ramosa-1, a temperature-sensitive mutant of Aspergillus niger.
4  from sweet potato and a fungal phytase from Aspergillus niger.
5 chuate utilization in the filamentous fungus Aspergillus niger.
6 isrupted WB cell walls, followed by SSF with Aspergillus niger.
7  enzymes (CAZymes) of the filamentous fungus Aspergillus niger.
8 nt of spatial gene expression in colonies of Aspergillus niger.
9 vestigate a glucoamylase from newly isolated Aspergillus niger.
10 spergillus oryzae, Aspergillus fumigatus and Aspergillus niger.
11 s cinerea as well as one from the saprotroph Aspergillus niger.
12 , Paecilomyces formosus, Rhizopus oryzae and Aspergillus niger.
13 d to a cell lysate of the filamentous fungus Aspergillus niger.
14 fitness landscape for the filamentous fungus Aspergillus niger.
15 ed stress response in the filamentous fungus Aspergillus niger.
16 utant recombinant gene has been expressed in Aspergillus niger.
17 ants at the active site of glucoamylase from Aspergillus niger.
18 phages (AMs)/30 min), followed by those from Aspergillus niger (2.4 nmol/1.0 x 10(6) AMs/30 min) and
19 ction included 181 Aspergillus fumigatus, 28 Aspergillus niger, 27 Aspergillus flavus, 22 Aspergillus
20 es of A. fumigatus, 235 of A. flavus, 162 of Aspergillus niger, 64 of Aspergillus terreus, and 15 of
21 ghest agreement was observed for isolates of Aspergillus niger (95%), which were particularly suscept
22 me: substrate ratio) inhibited the growth of Aspergillus niger, A. chevalieri, Trichoderma reesei, Py
23 me: substrate ratio) inhibited the growth of Aspergillus niger, A. chevalieri, Trichoderma reesei, Py
24  the analysis of small organics derived from Aspergillus niger, aflatoxigenic Aspergillus flavus, and
25                                              Aspergillus niger also precipitated lead oxalate during
26 d cofactors has been reported to exist in an Aspergillus niger amine oxidase AO-I.
27 ate the usage of a prolyl endopeptidase from Aspergillus niger (An-PEP) for HDX-MS.
28 Candida albicans, Aspergillus fumigatus, and Aspergillus niger and antibacterial activity against Esc
29 pression were obtained in Neurospora crassa, Aspergillus niger and Aspergillus awamori by codon optim
30 ine oxidase (MAO) was recently isolated from Aspergillus niger and cloned.
31   Here we report identification of tigA from Aspergillus niger and erp38 from Neurospora crassa, two
32 cient mediators of glucose oxidase (GO) from Aspergillus niger and horseradish peroxidase (HRP).
33 uginosa, Escherichia coli, Candida albicans, Aspergillus niger and Microsporum gypseum with minimal i
34                                              Aspergillus niger and Paecilomyces javanicus grew in 5 m
35                                              Aspergillus niger and Paecilomyces javanicus were grown
36 yphi, Candida albicans, Rhizopus stolonifer, Aspergillus niger and Penicillium notatum when compared
37  tolerance of two typical filamentous fungi, Aspergillus niger and Penicillium oxalicum.
38  industry) and brandy distillery wastes with Aspergillus niger and Rhizopus oligosporus were investig
39                                              Aspergillus niger and S. himantioides were capable of so
40                The ability of the soil fungi Aspergillus niger and Serpula himantioides to tolerate a
41 fied extracts of NADPH eukNR from the fungus Aspergillus niger and the (15)epsilon for NADH eukNR fro
42 by organic-acid-producing fungi, for example Aspergillus niger, and that plants grown with pyromorphi
43 ed from a commercial enzyme preparation from Aspergillus niger, and the encoding gene was identified.
44 ausing parasite Plasmodium vivax, the fungus Aspergillus niger, and the TEM-family of beta-lactamase
45 ependent glucose dehydrogenase, derived from Aspergillus niger (AnGDH), was characterized.
46                   Apergillus carbonarius and Aspergillus niger are the principal fungi that attack ta
47 nzyme endopolygalacturonase II (EPG-II) from Aspergillus niger as it binds to an oligosaccharide subs
48 fficacy evaluation as edible coating against Aspergillus niger, Aspergillus luchuensis, and Penicilli
49 anulosus, Aspergillus (Emericella) nidulans, Aspergillus niger, Aspergillus restrictus, Aspergillus s
50 Aspergillus fumigatus, Aspergillus nidulans, Aspergillus niger, Aspergillus terreus, Aspergillus ustu
51 d Aspergillus flavus, Aspergillus fumigatus, Aspergillus niger, Aspergillus terreus, Fusarium spp., P
52  (Aspergillus fumigatus, Aspergillus flavus, Aspergillus niger, Aspergillus terreus, Scedosporium pro
53 ns Zygosaccharomyces bailii (ATCC 42476) and Aspergillus niger (ATCC 6275 (M68)).
54 l fungi with geoactive properties, including Aspergillus niger, Beauveria caledonica and Serpula hima
55                          In the present work Aspergillus niger beta-glucosidase is immobilized within
56 ifungal efficacy against Penicillium sp. and Aspergillus niger but low effective against Rhizopus sp.
57                The orthologous transcript of Aspergillus niger can be alternatively spliced; the exon
58                                We found that Aspergillus niger CDA strongly prefers a GlcNAc sugar un
59 e, we determined the crystal structure of an Aspergillus niger CDA.
60 C in pH 6.5 buffer more than doubled that of Aspergillus niger cellulase at pH 5 and 37 degrees C and
61                              Trichoderma and Aspergillus niger cellulases activities were determined
62 ssisted solid-state fermentation (SSF) using Aspergillus niger CGMCC 3.6189.
63 (Cu2 (CO3 )(OH)2 ) and bioaccumulated within Aspergillus niger colonies when grown on different inorg
64                    The geoactive soil fungus Aspergillus niger colonized monazite in solid and liquid
65 ture filtrate of an over-producing strain of Aspergillus niger containing multiple copies of the enco
66      Therefore, ferulic acid esterase A from Aspergillus niger contributes to total plant cell wall d
67 nd purified alpha-casein (alphas-CN) with an Aspergillus niger derived prolyl endoproteinase (An-PEP)
68 A cellulose-specific endoglucanase (CEG from Aspergillus niger) did not cause cell wall creep, either
69             Lead oxalate was precipitated by Aspergillus niger during bioleaching of natural and synt
70     The enzyme PGC is produced by the fungus Aspergillus niger during invasion of plant cell walls.
71 f the anode consists of glucose oxidase from Aspergillus niger electrically "wired" by polymer I, hav
72 acterisation of the eroA and ervA genes from Aspergillus niger, encoding functional orthologues of S.
73 sing Escherichia coli expressing recombinant Aspergillus niger epoxide hydrolase as the model enzyme
74          Two quinate permeases isolated from Aspergillus niger facilitates shikimate translocation to
75                                        Using Aspergillus niger Fdc1 as a model system, we reveal that
76  biosynthetically produced starting from the Aspergillus niger fed on cheap materials.
77 d for their ability to enhance the growth of Aspergillus niger for citric acid production via submerg
78 rom both live Arabidopsis thaliana plant and Aspergillus niger fungal species are presented.
79                                          The Aspergillus niger genome contains four genes that encode
80  the emulsions assays were conducted against Aspergillus niger given its strong resistance and its re
81  sites of the starch-binding domain (SBD) of Aspergillus niger glucoamylase 1 (GA-I) with substrate h
82  as a dough and bread improver, similarly to Aspergillus niger glucose oxidase (GOX).
83                      Saprobic fungi, such as Aspergillus niger, grow as colonies consisting of a netw
84  binding domain (SBD) of glucoamylase 1 from Aspergillus niger has been determined by heteronuclear m
85 from Kluyveromyces marxianus NRRL Y 7571 and Aspergillus niger in an aqueous-organic system.
86 gh resolution x-ray structures of a PME from Aspergillus niger in deglycosylated and Asn-linked N-ace
87 f a common saprophytic and geoactive fungus, Aspergillus niger, in the presence of a solid source of
88 ve the secretion of heterologous proteins in Aspergillus niger include the manipulation of chaperones
89                                              Aspergillus niger is known to secrete large amounts of b
90 t, the flavin-linked sulfhydryl oxidase from Aspergillus niger is related to the pyridine nucleotide-
91  demonstrated a superior performance against Aspergillus niger, isolated from spoiled pomegranate, co
92                              Eighty putative Aspergillus niger isolates were selected for sequencing,
93 zymes in a fungal protein expression system (Aspergillus niger) leads to significantly enhanced speci
94                       Monoamine oxidase from Aspergillus niger (MAO-N) is a flavoenzyme that catalyse
95 "toolbox" of monoamine oxidase variants from Aspergillus niger (MAO-N) which display remarkable subst
96 H) and enzymatic (endopolygalacturonase from Aspergillus niger) methods.
97  oahA gene restores oxalate production in an Aspergillus niger mutant strain, lacking a functional oa
98 with Botrytis cinerea, Penicillium expansum, Aspergillus niger or A. carbonarius.
99           The three-dimensional structure of Aspergillus niger pectin lyase B (PLB) has been determin
100 gether with recombinant proteins: the fungal Aspergillus niger PhyA or the bacterial Escherichia coli
101 ercially-relevant recombinant glycoproteins (Aspergillus niger phytase and anti-HIV antibody 2G12) pr
102                                              Aspergillus niger phytase shares 66% sequence identity,
103 tion because of either the expression of the Aspergillus niger polygalacturonase II (AnPGII; 35S:AnPG
104 y and 38% identity with glucose oxidase from Aspergillus niger, possesses an amino-terminal sequence
105 se, and alpha-rhamnosidase from a commercial Aspergillus niger preparation, were immobilized onto acr
106 ostproline cleaving enzymes (PPCEs), such as Aspergillus niger prolyl endopeptidase (AnPEP) and nepro
107                The hydrolytic specificity of Aspergillus niger prolyl endoproteinase (An-PEP) on puri
108       Oral supplementation with enzymes like Aspergillus niger propyl-endoprotease (AN-PEP), which ca
109  analysis of Cdc42, Rac1 and Rho function in Aspergillus niger provides the first global perspective
110 neered strains of Aspergillus pseudoterreus, Aspergillus niger, Pseudomonas putida and Rhodosporidium
111 moyl esterase, ferulic acid esterase A, from Aspergillus niger releases ferulic acid and 5-5- and 8-O
112 d and identified as Penicillium oxalicum and Aspergillus niger respectively in this study.
113     Aspergillus tubingensis, a member of the Aspergillus niger species complex, was most prevalent fr
114               We report a pseudo-outbreak of Aspergillus niger that followed building construction in
115    We obtained a candidate fungal extract of Aspergillus niger that inhibited the interaction between
116  successful history of citrate production in Aspergillus niger, the molecular mechanism of citrate ac
117           Like the native OxDC isolated from Aspergillus niger, the recombinant, bacterial OxDC from
118                                           In Aspergillus niger, the target protein is normally fused
119 s study, the ability of the geoactive fungus Aspergillus niger to colonize and transform manganese no
120 ility of a ubiquitous geoactive soil fungus, Aspergillus niger, to affect the mobility of REE in mona
121  the fungal pathogens, Penicillium italicum, Aspergillus niger, Trichoderma harzianum and Botrytis ci
122 c properties of ferulic acid esterase A from Aspergillus niger using a range of synthetic ethyl ester
123                                              Aspergillus niger was able to colonize and penetrate man
124                                              Aspergillus niger was capable of solubilizing natural (f
125 tnC from the kotanin biosynthetic pathway of Aspergillus niger was expressed in Saccharomyces cerevis
126                        The phytase gene from Aspergillus niger was inserted into soybean transformati
127           In this work, the geoactive fungus Aspergillus niger was investigated for struvite transfor
128 his work, the transformation of Mn oxides by Aspergillus niger was investigated using a Co-bearing ma
129 alyze the process, and beta-glucosidase from Aspergillus niger was selected.
130                    The enzyme, purified from Aspergillus Niger, was immobilized on zinc oxide nanopar
131 n Trichoderma reesei (Hypocrea jecorina) and Aspergillus niger, we identified the genes lxr4 and xhrA
132 ic melanin or fungal pigments extracted from Aspergillus niger were analyzed by MALDI-TOF and MALDI-q
133 stress response of the geoactive soil fungus Aspergillus niger were investigated in the presence of t
134 ucose-resistant mutant of a locally isolated Aspergillus niger were purified to apparent homogeneity.
135 he oxidoreductase glucose oxidase (GOx) from Aspergillus niger, which is the most frequently applied

 
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