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1 and calcium content as thermally inactivated manganese peroxidase.
5 f calcium to prevent thermal inactivation of manganese peroxidase and the rate of calcium binding dec
6 site with both compound I and compound II of manganese peroxidase and to determine whether phenolic s
7 The 16 encoded enzymes include 13 putative manganese peroxidases and one generic peroxidase but mos
8 me c peroxidase, horseradish peroxidase, and manganese peroxidase, and (d) examination of the crystal
9 conformational changes proposed to occur in manganese peroxidase as a result of the binding and rele
11 s that occurred during thermal incubation of manganese peroxidase could be explained by the loss of t
12 stal heme environment, thermally inactivated manganese peroxidase did not react with hydrogen peroxid
14 igates whether compound I and compound II of manganese peroxidase from the white-rot fungus Phaneroch
16 and 55 degrees C, MnII and CdII both protect manganese peroxidase from thermal denaturation more effi
19 ulfonic acid, dipotassium salt (bis-ANS), to manganese peroxidase indicated that the active, calcium-
20 tations R177A and R177K in the gene encoding manganese peroxidase isozyme 1 (mnp1) from Phanerochaete
21 190L, F190I, and F190A, in the gene encoding manganese peroxidase isozyme 1 (mnp1) from Phanerochaete
22 , E39Q, and E35Q-D179N, in the gene encoding manganese peroxidase isozyme 1 (mnp1) from Phanerochaete
23 in MnII binding at the MnII binding site of manganese peroxidase isozyme 1 (MnP1) of Phanerochaete c
24 esis that the synergy of Fenton reaction and manganese peroxidase might play an important role in DR5
26 nce CcP contains both Trp51 and Trp191 while manganese peroxidase (MnP) contains phenylalanine residu
29 cytochrome c peroxidase that closely mimics manganese peroxidase (MnP) has been characterized by bot
34 ases, including the lignin degrading enzymes manganese peroxidase (MnP), lignin peroxidase (LiP), and
35 detectable values of 7.9% for free laccase, manganese peroxidase (MnP), lignin peroxidase (LiP), res
39 on of these genes together with a lignolytic manganese peroxidase, multiple copper radical oxidases,
43 oposed that, at lower pH, calcium binding to manganese peroxidase was more thermodynamically favorabl
44 hat the heme iron of the inactivated form of manganese peroxidase was predominantly in a low-spin sta
46 alcium to the distal calcium binding site of manganese peroxidase was studied by optical absorption s
47 idized by the radical products of lignin and manganese peroxidases, whereas cellulose and hemicellulo
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