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1 n the electrochemical properties of CDH from Phanerochaete chrysosporium (PcCDH) and Ceriporiopsis su
3 etalloenzyme produced by the wood-rot fungus Phanerochaete chrysosporium as an essential component of
4 e in the active site of glyoxal oxidase from Phanerochaete chrysosporium based on a combination of sp
5 of manganese peroxidase isozyme 1 (MnP1) of Phanerochaete chrysosporium by examining two mutants: R1
8 stabilized and improved Avicel hydrolysis by Phanerochaete chrysosporium CBH II, which is only 55-56%
9 lose-binding tunnel that is more closed than Phanerochaete chrysosporium Cel7D and more open than Hyp
12 ional crystal structure of the basidiomycete Phanerochaete chrysosporium GH61D LPMO, and, for the fir
13 gnin peroxidase (LiP) from the basidiomycete Phanerochaete chrysosporium has been determined to 2.6 A
16 nditions, the lignin-degrading basidiomycete Phanerochaete chrysosporium mineralizes 2,4, 6-trichloro
18 peroxidases (LiP) from the white-rot fungus Phanerochaete chrysosporium oxidize veratryl alcohol (VA
20 acterization of one isoform of this class in Phanerochaete chrysosporium revealed original properties
22 sequenced the 30-million base-pair genome of Phanerochaete chrysosporium strain RP78 using a whole ge
23 ns with the closely related white-rot fungus Phanerochaete chrysosporium support an evolutionary shif
24 rom the basidiomycetes Agaricus bisporus and Phanerochaete chrysosporium that were used successfully
25 n peroxidase (MnP) from the white-rot fungus Phanerochaete chrysosporium to investigate the role of t
27 nganese peroxidase from the white-rot fungus Phanerochaete chrysosporium utilize the same Mn-binding
28 g manganese peroxidase isozyme 1 (mnp1) from Phanerochaete chrysosporium was generated by overlap ext
29 nganese peroxidase from the white-rot fungus Phanerochaete chrysosporium was very susceptible to ther
32 the lignin-degrading basidiomycetous fungus, Phanerochaete chrysosporium, catalyzes the oxidation of
33 e dehydrogenase (CDH) from the basidiomycete Phanerochaete chrysosporium, immobilised in an enzyme re
34 g manganese peroxidase isozyme 1 (mnp1) from Phanerochaete chrysosporium, was created by overlap exte
35 H [F(CF2)6CH2CH2OH] by the white-rot fungus, Phanerochaete chrysosporium, was investigated in laborat
36 pared the abilities of a known LiP producer, Phanerochaete chrysosporium, with those of a reported no
40 demonstrated that manganese peroxidase from Phanerochaete chrysosporiumwas susceptible to thermal in
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