ライフサイエンスコーパス: Aspergillus niger

1 enzymes (CAZymes) of the filamentous fungus Aspergillus niger.

2 nt of spatial gene expression in colonies of Aspergillus niger.

3 vestigate a glucoamylase from newly isolated Aspergillus niger.

4 spergillus oryzae, Aspergillus fumigatus and Aspergillus niger.

5 s cinerea as well as one from the saprotroph Aspergillus niger.

6 d to a cell lysate of the filamentous fungus Aspergillus niger.

7 fitness landscape for the filamentous fungus Aspergillus niger.

8 ed stress response in the filamentous fungus Aspergillus niger.

9 utant recombinant gene has been expressed in Aspergillus niger.

10 ants at the active site of glucoamylase from Aspergillus niger.

11 ia coli could be applied to the isozyme from Aspergillus niger.

12 e of two esterases (FAE-III and CinnAE) from Aspergillus niger.

13 ramosa-1, a temperature-sensitive mutant of Aspergillus niger.

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

15 ction included 181 Aspergillus fumigatus, 28 Aspergillus niger, 27 Aspergillus flavus, 22 Aspergillus

16 es of A. fumigatus, 235 of A. flavus, 162 of Aspergillus niger, 64 of Aspergillus terreus, and 15 of

17 ghest agreement was observed for isolates of Aspergillus niger (95%), which were particularly suscept

18 Aspergillus niger also precipitated lead oxalate during

19 d cofactors has been reported to exist in an Aspergillus niger amine oxidase AO-I.

20 ate the usage of a prolyl endopeptidase from Aspergillus niger (An-PEP) for HDX-MS.

21 Candida albicans, Aspergillus fumigatus, and Aspergillus niger and antibacterial activity against Esc

22 pression were obtained in Neurospora crassa, Aspergillus niger and Aspergillus awamori by codon optim

23 ine oxidase (MAO) was recently isolated from Aspergillus niger and cloned.

24 Here we report identification of tigA from Aspergillus niger and erp38 from Neurospora crassa, two

25 cient mediators of glucose oxidase (GO) from Aspergillus niger and horseradish peroxidase (HRP).

26 uginosa, Escherichia coli, Candida albicans, Aspergillus niger and Microsporum gypseum with minimal i

27 Aspergillus niger and Paecilomyces javanicus grew in 5 m

28 Aspergillus niger and Paecilomyces javanicus were grown

29 yphi, Candida albicans, Rhizopus stolonifer, Aspergillus niger and Penicillium notatum when compared

30 industry) and brandy distillery wastes with Aspergillus niger and Rhizopus oligosporus were investig

31 Aspergillus niger and S. himantioides were capable of so

32 The ability of the soil fungi Aspergillus niger and Serpula himantioides to tolerate a

33 fied extracts of NADPH eukNR from the fungus Aspergillus niger and the (15)epsilon for NADH eukNR fro

34 by organic-acid-producing fungi, for example Aspergillus niger, and that plants grown with pyromorphi

35 ed from a commercial enzyme preparation from Aspergillus niger, and the encoding gene was identified.

36 ausing parasite Plasmodium vivax, the fungus Aspergillus niger, and the TEM-family of beta-lactamase

37 ependent glucose dehydrogenase, derived from Aspergillus niger (AnGDH), was characterized.

38 nzyme endopolygalacturonase II (EPG-II) from Aspergillus niger as it binds to an oligosaccharide subs

39 anulosus, Aspergillus (Emericella) nidulans, Aspergillus niger, Aspergillus restrictus, Aspergillus s

40 Aspergillus fumigatus, Aspergillus nidulans, Aspergillus niger, Aspergillus terreus, Aspergillus ustu

41 d Aspergillus flavus, Aspergillus fumigatus, Aspergillus niger, Aspergillus terreus, Fusarium spp., P

42 (Aspergillus fumigatus, Aspergillus flavus, Aspergillus niger, Aspergillus terreus, Scedosporium pro

43 l fungi with geoactive properties, including Aspergillus niger, Beauveria caledonica and Serpula hima

44 In the present work Aspergillus niger beta-glucosidase is immobilized within

45 Trichoderma and Aspergillus niger cellulases activities were determined

46 (Cu2 (CO3 )(OH)2 ) and bioaccumulated within Aspergillus niger colonies when grown on different inorg

47 ture filtrate of an over-producing strain of Aspergillus niger containing multiple copies of the enco

48 Therefore, ferulic acid esterase A from Aspergillus niger contributes to total plant cell wall d

49 nd purified alpha-casein (alphas-CN) with an Aspergillus niger derived prolyl endoproteinase (An-PEP)

50 A cellulose-specific endoglucanase (CEG from Aspergillus niger) did not cause cell wall creep, either

51 Lead oxalate was precipitated by Aspergillus niger during bioleaching of natural and synt

52 The enzyme PGC is produced by the fungus Aspergillus niger during invasion of plant cell walls.

53 f the anode consists of glucose oxidase from Aspergillus niger electrically "wired" by polymer I, hav

54 acterisation of the eroA and ervA genes from Aspergillus niger, encoding functional orthologues of S.

55 sing Escherichia coli expressing recombinant Aspergillus niger epoxide hydrolase as the model enzyme

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

57 rom both live Arabidopsis thaliana plant and Aspergillus niger fungal species are presented.

58 The Aspergillus niger genome contains four genes that encode

59 the emulsions assays were conducted against Aspergillus niger given its strong resistance and its re

60 sites of the starch-binding domain (SBD) of Aspergillus niger glucoamylase 1 (GA-I) with substrate h

61 as a dough and bread improver, similarly to Aspergillus niger glucose oxidase (GOX).

62 binding domain (SBD) of glucoamylase 1 from Aspergillus niger has been determined by heteronuclear m

63 from Kluyveromyces marxianus NRRL Y 7571 and Aspergillus niger in an aqueous-organic system.

64 gh resolution x-ray structures of a PME from Aspergillus niger in deglycosylated and Asn-linked N-ace

65 ve the secretion of heterologous proteins in Aspergillus niger include the manipulation of chaperones

66 Aspergillus niger is known to secrete large amounts of b

67 t, the flavin-linked sulfhydryl oxidase from Aspergillus niger is related to the pyridine nucleotide-

68 zymes in a fungal protein expression system (Aspergillus niger) leads to significantly enhanced speci

69 Monoamine oxidase from Aspergillus niger (MAO-N) is a flavoenzyme that catalyse

70 "toolbox" of monoamine oxidase variants from Aspergillus niger (MAO-N) which display remarkable subst

71 H) and enzymatic (endopolygalacturonase from Aspergillus niger) methods.

72 oahA gene restores oxalate production in an Aspergillus niger mutant strain, lacking a functional oa

73 The three-dimensional structure of Aspergillus niger pectin lyase B (PLB) has been determin

74 ercially-relevant recombinant glycoproteins (Aspergillus niger phytase and anti-HIV antibody 2G12) pr

75 Aspergillus niger phytase shares 66% sequence identity,

76 tion because of either the expression of the Aspergillus niger polygalacturonase II (AnPGII; 35S:AnPG

77 y and 38% identity with glucose oxidase from Aspergillus niger, possesses an amino-terminal sequence

78 se, and alpha-rhamnosidase from a commercial Aspergillus niger preparation, were immobilized onto acr

79 The hydrolytic specificity of Aspergillus niger prolyl endoproteinase (An-PEP) on puri

80 Oral supplementation with enzymes like Aspergillus niger propyl-endoprotease (AN-PEP), which ca

81 analysis of Cdc42, Rac1 and Rho function in Aspergillus niger provides the first global perspective

82 moyl esterase, ferulic acid esterase A, from Aspergillus niger releases ferulic acid and 5-5- and 8-O

83 d and identified as Penicillium oxalicum and Aspergillus niger respectively in this study.

84 We report a pseudo-outbreak of Aspergillus niger that followed building construction in

85 We obtained a candidate fungal extract of Aspergillus niger that inhibited the interaction between

86 successful history of citrate production in Aspergillus niger, the molecular mechanism of citrate ac

87 Like the native OxDC isolated from Aspergillus niger, the recombinant, bacterial OxDC from

88 In Aspergillus niger, the target protein is normally fused

89 the fungal pathogens, Penicillium italicum, Aspergillus niger, Trichoderma harzianum and Botrytis ci

90 c properties of ferulic acid esterase A from Aspergillus niger using a range of synthetic ethyl ester

91 tnC from the kotanin biosynthetic pathway of Aspergillus niger was expressed in Saccharomyces cerevis

92 The phytase gene from Aspergillus niger was inserted into soybean transformati

93 alyze the process, and beta-glucosidase from Aspergillus niger was selected.

94 n Trichoderma reesei (Hypocrea jecorina) and Aspergillus niger, we identified the genes lxr4 and xhrA

95 ic melanin or fungal pigments extracted from Aspergillus niger were analyzed by MALDI-TOF and MALDI-q

96 ucose-resistant mutant of a locally isolated Aspergillus niger were purified to apparent homogeneity.

97 he oxidoreductase glucose oxidase (GOx) from Aspergillus niger, which is the most frequently applied