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1 ding lignin peroxidase (LiP) isozyme H8 from Phanerochaete chrysosporium.
2 enzyme produced by ligninolytic cultures of Phanerochaete chrysosporium.
3 --D179E triple variant of MnP isozyme 1 from Phanerochaete chrysosporium.
4 tic polysaccharide monooxygenase (LPMO) from Phanerochaete chrysosporium.
5 ichum gloesporioides, Fusarium concentricum, Phanerochaete chrysosporium, and Penicillium rolfsii.
7 etalloenzyme produced by the wood-rot fungus Phanerochaete chrysosporium as an essential component of
8 e in the active site of glyoxal oxidase from Phanerochaete chrysosporium based on a combination of sp
9 of manganese peroxidase isozyme 1 (MnP1) of Phanerochaete chrysosporium by examining two mutants: R1
12 the lignin-degrading basidiomycetous fungus, Phanerochaete chrysosporium, catalyzes the oxidation of
13 stabilized and improved Avicel hydrolysis by Phanerochaete chrysosporium CBH II, which is only 55-56%
14 lose-binding tunnel that is more closed than Phanerochaete chrysosporium Cel7D and more open than Hyp
16 e (AfGDH) and an electron transfer domain of Phanerochaete chrysosporium-derived cellobiose dehydroge
18 ional crystal structure of the basidiomycete Phanerochaete chrysosporium GH61D LPMO, and, for the fir
19 gnin peroxidase (LiP) from the basidiomycete Phanerochaete chrysosporium has been determined to 2.6 A
20 gs of the study suggest that LiP produced by Phanerochaete chrysosporium has the potential to be used
21 e dehydrogenase (CDH) from the basidiomycete Phanerochaete chrysosporium, immobilised in an enzyme re
24 nditions, the lignin-degrading basidiomycete Phanerochaete chrysosporium mineralizes 2,4, 6-trichloro
25 (LiP), an extracellular enzyme purified from Phanerochaete chrysosporium NK-1 isolated from a forest
27 peroxidases (LiP) from the white-rot fungus Phanerochaete chrysosporium oxidize veratryl alcohol (VA
29 n the electrochemical properties of CDH from Phanerochaete chrysosporium (PcCDH) and Ceriporiopsis su
30 acterization of one isoform of this class in Phanerochaete chrysosporium revealed original properties
32 sequenced the 30-million base-pair genome of Phanerochaete chrysosporium strain RP78 using a whole ge
33 ns with the closely related white-rot fungus Phanerochaete chrysosporium support an evolutionary shif
34 rom the basidiomycetes Agaricus bisporus and Phanerochaete chrysosporium that were used successfully
35 n peroxidase (MnP) from the white-rot fungus Phanerochaete chrysosporium to investigate the role of t
37 nganese peroxidase from the white-rot fungus Phanerochaete chrysosporium utilize the same Mn-binding
38 g manganese peroxidase isozyme 1 (mnp1) from Phanerochaete chrysosporium was generated by overlap ext
39 nganese peroxidase from the white-rot fungus Phanerochaete chrysosporium was very susceptible to ther
40 g manganese peroxidase isozyme 1 (mnp1) from Phanerochaete chrysosporium, was created by overlap exte
41 H [F(CF2)6CH2CH2OH] by the white-rot fungus, Phanerochaete chrysosporium, was investigated in laborat
44 pared the abilities of a known LiP producer, Phanerochaete chrysosporium, with those of a reported no