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1 which is <6 A from the flavin C(4a) atom in choline oxidase.
2 1.86 A resolution X-ray crystal structure of choline oxidase.
3 eptor in the tunneling reaction catalyzed by choline oxidase.
4 located on the solvent accessible surface of choline oxidase.
5 e reaction of choline oxidation catalyzed by choline oxidase.
6 e reaction of choline oxidation catalyzed by choline oxidase.
7 oning of the substrate in the active site of choline oxidase.
8 g characterization of the resulting forms of choline oxidase.
9 hydrogen peroxide in a reaction catalyzed by choline oxidase.
10 enings in serum is reduced by treatment with choline oxidase.
11 he reaction of flavin oxidation catalyzed by choline oxidase.
13 fects with 1,2-[2H4]choline as substrate for choline oxidase at 0.2 mM oxygen to gain insights on the
14 ues were observed as compared with wild-type choline oxidase at pH 10 and 25 degrees C, with no signi
15 ctive hypothesis of whether the mechanism of choline oxidase can be extended to other flavin-dependen
16 in codA transgenic plants, as a byproduct of choline oxidase-catalyzed GB synthesis, might activate t
24 coupling of acetylcholinesterase (AChE) and choline oxidase (ChO) by their reaction with glutaraldeh
25 ) (PoPD) and acetylcholinesterase (AChE) and choline oxidase (ChO) enzymes were fabricated on carbon
26 a mixture of acetylcholinesterase (AChE) and choline oxidase (ChO) onto nanocomposite of chitosan (CH
27 ing enzymes, acetylcholinesterase (AChE) and choline oxidase (ChO), on the surface of iron oxide nano
30 is based on measurement of H2O2 generated by choline oxidase (ChOx) in the presence of choline (Ch).
31 to form choline that is in turn oxidized by choline oxidase (ChOx) to produce betaine and H(2)O(2),
32 ACh to choline, which in turn is oxidized by choline oxidase (ChOx) to produce betaine and H2O2 that
34 he wild-type and a number of mutant forms of choline oxidase from Arthrobacter globiformis have recen
35 ine-oxidizing enzyme is the flavin-dependent choline oxidase from Arthrobacter globiformis, for which
37 ults presented in this study suggest that in choline oxidase, His(466) modulates the electrophilicity
39 the protein charge near the FAD N(1) locus, choline oxidase lost the ability to stabilize negative c
40 d oxidation of glucose, acetylcholinesterase/choline oxidase-mediated hydrolysis and oxidation of ace
41 is data on His466, allow us to conclude that choline oxidase must necessarily utilize a strategy for
42 fer reaction in which choline is oxidized by choline oxidase occurs quantum mechanically within a pre
43 We propose that the side chain of Val464 in choline oxidase provides a nonpolar site that is require
44 ected two enzymes (glucose dehydrogenase and choline oxidase) that react with their respective model
45 cent study showed that in the active site of choline oxidase the protein positive charge is provided
46 nt determination of the crystal structure of choline oxidase to a resolution of 1.86 A established th
47 e of Arthrobacter globiformis, which encodes choline oxidase to catalyze the conversion of choline to
48 The hydride transfer reaction catalyzed by choline oxidase under irreversible regime, i.e., at satu
49 ate the mechanism for substrate oxidation by choline oxidase using both steady-state kinetics and rap
53 sm for the oxidation of choline catalyzed by choline oxidase was recently elucidated by using kinetic
54 served asparagine residue at position 510 in choline oxidase was replaced with alanine, aspartate, hi
55 nserved histidine residue at position 466 of choline oxidase was replaced with an alanine residue by
56 talytic parameters with respect to wild-type choline oxidase were seen in the Asn510Ala enzyme, with
57 ransgenic plants express codA and synthesize choline oxidase, while accumulating GB in their leaves a
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