ライフサイエンスコーパス: Chrysosporium

1 ases from H. irregulare, H. jecorina, and P. chrysosporium.

2 ished cellulolytic capability relative to P. chrysosporium.

3 e genome analysis of C. subvermispora and P. chrysosporium.

4 rom other morphologically similar species of Chrysosporium.

5 roxidase (LiP) isozyme H8 from Phanerochaete chrysosporium.

6 ed by ligninolytic cultures of Phanerochaete chrysosporium.

7 variant of MnP isozyme 1 from Phanerochaete chrysosporium.

8 The isolate was later identified as the Chrysosporium anamorph of Nannizziopsis vriesii by seque

9 were produced by homologous expression in P. chrysosporium and were purified to homogeneity.

10 The lignin peroxidases of Phanerochaete chrysosporium are encoded by a minimum of 10 closely rel

11 roduced by the wood-rot fungus Phanerochaete chrysosporium as an essential component of its extracell

12 tion, including being grouped with the genus Chrysosporium at one time.

13 e site of glyoxal oxidase from Phanerochaete chrysosporium based on a combination of spectroscopic an

14 lignin that are as efficient as those in P. chrysosporium but that do not depend on LiP.

15 t half of dimer mineralization in wood by P. chrysosporium but was responsible for no more than 6-7%

16 peroxidase isozyme 1 (MnP1) of Phanerochaete chrysosporium by examining two mutants: R177A and R177K.

17 Lignin peroxidase (LiP) from Phanerochaete chrysosporium catalyzes irreversible oxidative damage to

18 Lignin peroxidase (LiP) from Phanerochaete chrysosporium catalyzes the H2O2 dependent one- and two-

19 rading basidiomycetous fungus, Phanerochaete chrysosporium, catalyzes the oxidation of MnII to MnIII.

20 improved Avicel hydrolysis by Phanerochaete chrysosporium CBH II, which is only 55-56% identical to

21 unnel that is more closed than Phanerochaete chrysosporium Cel7D and more open than Hypocrea jecorina

22 Phanerochaete chrysosporium completely degrades lignocellulose.

23 vermispora culture filtrates, but none in P. chrysosporium cultures.

24 neralized all of the models as rapidly as P. chrysosporium did.

25 The mutant enzymes were expressed in P. chrysosporium during primary metabolic growth under the

26 The mutant genes were expressed in P. chrysosporium during primary metabolic growth under the

27 The mutant genes were expressed in P. chrysosporium during primary metabolic growth under the

28 In the present work, we used Phanerochaete chrysosporium for biochemical characterization and analy

29 predicted to encode laccases, whereas the P. chrysosporium genome contains none.

30 The P. chrysosporium genome reveals an impressive array of gene

31 ce for surface translation indicates that P. chrysosporium GH61D exhibits energy wells whose spacing

32 structure of the basidiomycete Phanerochaete chrysosporium GH61D LPMO, and, for the first time, measu

33 e (LiP) from the basidiomycete Phanerochaete chrysosporium has been determined to 2.6 A resolution by

34 These results demonstrate that P. chrysosporium has the necessary biochemical mechanisms t

35 e (CDH) from the basidiomycete Phanerochaete chrysosporium, immobilised in an enzyme reactor.

36 to the model white-rot species Phanerochaete chrysosporium in the PCA.

37 Invasive Chrysosporium infections typically occur in impaired hos

38 this matter, the reported cases of invasive Chrysosporium infections were reviewed.

39 ncode peroxidases structurally similar to P. chrysosporium lignin peroxidase and, following heterolog

40 Phanerochaete chrysosporium manganese peroxidase (MnP) [isoenzyme H4]

41 ant is the cation radical of the secreted P. chrysosporium metabolite veratryl alcohol.

42 P. chrysosporium mineralized all three models rapidly in de

43 lignin-degrading basidiomycete Phanerochaete chrysosporium mineralizes 2,4, 6-trichlorophenol.

44 Moreover, methods for the study of P. chrysosporium must be applicable to solid substrate as w

45 We grew Phanerochaete chrysosporium on wood sections in the presence of oxidan

46 tion and characterization of the new species Chrysosporium ophiodiicola from a mycotic granuloma of a

47 LiP) from the white-rot fungus Phanerochaete chrysosporium oxidize veratryl alcohol (VA) by two elect

48 anganese peroxidase (MnP) from Phanerochaete chrysosporium oxidizes nonphenolic beta-1 diarylpropane

49 hemical properties of CDH from Phanerochaete chrysosporium (PcCDH) and Ceriporiopsis subvermispora (C

50 were produced by homologous expression in P. chrysosporium, purified to homogeneity, and characterize

51 bered 13 and five in C. subvermispora and P. chrysosporium, respectively.

52 f one isoform of this class in Phanerochaete chrysosporium revealed original properties.

53 Phanerochaete chrysosporium simultaneously degrades lignin and cellulo

54 y differentiated the genus Emmonsia from the Chrysosporium species.

55 30-million base-pair genome of Phanerochaete chrysosporium strain RP78 using a whole genome shotgun a

56 osely related white-rot fungus Phanerochaete chrysosporium support an evolutionary shift from white-r

57 omycetes Agaricus bisporus and Phanerochaete chrysosporium that were used successfully to control the

58 MnP) from the white-rot fungus Phanerochaete chrysosporium to investigate the role of the axial ligan

59 In this study, P. chrysosporium transformed 6:2 FTOH to perfluorocarboxyli

60 anganese peroxidase (MnP) from Phanerochaete chrysosporium undergoes a pH-dependent conformational ch

61 dase from the white-rot fungus Phanerochaete chrysosporium utilize the same Mn-binding site for catal

62 roxidase isozyme 1 (mnp1) from Phanerochaete chrysosporium was generated by overlap extension with th

63 dase from the white-rot fungus Phanerochaete chrysosporium was very susceptible to thermal inactivati

64 roxidase isozyme 1 (mnp1) from Phanerochaete chrysosporium, was created by overlap extension, using t

65 H2OH] by the white-rot fungus, Phanerochaete chrysosporium, was investigated in laboratory studies.

66 s of ligninolytic enzymes from Phanerochaete chrysosporium were evaluated.

67 roxidase isozyme 1 (mnp1) from Phanerochaete chrysosporium were generated.

68 ities of a known LiP producer, Phanerochaete chrysosporium, with those of a reported nonproducer, Cer

69 ophilicum, Xerochrysium xerophilum (formerly Chrysosporium xerophilum) and Xeromyces bisporus, were p

70 on limited in vitro susceptibility data for Chrysosporium zonatum, amphotericin B is the most active