ライフサイエンスコーパス: oxidizing enzyme

1 licas of the peroxidases and cytochrome P450 oxidizing enzymes.

2 n high-pH (hpH) signal common to all sulfite oxidizing enzymes.

3 ric sarcosine oxidase (MSOX) family of amine oxidizing enzymes.

4 -associated heterotrophic bacteria, and NADH-oxidizing enzymes.

5 a variety of genes encoding free fatty acid-oxidizing enzymes.

6 ved within the family of L-alpha-hydroxyacid oxidizing enzymes.

7 aldehyde or oxygen radicals by fetal ethanol-oxidizing enzymes.

8 is one of only two identified human m6A RNA oxidizing enzymes and is a potential target for cancer t

9 ), a transcriptional activator of fatty acid oxidizing enzymes, and uncoupling protein 3 (UCP3), a th

10 Based on sequence analysis, these phosphite-oxidizing enzymes are related to nucleotide-diphosphate-

11 f the tetramanganese-oxide core of the water-oxidizing enzyme during biogenesis.

12 eviously described bacterial d- or l-lactate oxidizing enzymes (Escherichia coli genes dld and lldD)

13 The pros and cons of using each methane-oxidizing enzyme for Bio-GTL are considered in detail.

14 ogenetically distinct from the monomeric GAP-oxidizing enzyme found previously in several Archaea.

15 results were observed for samples of sulfite-oxidizing enzymes from other organisms that were previou

16 Mitomycin C hydroquinone-oxidizing enzymes give rise to a new mechanism by which

17 All reported sulfite-oxidizing enzymes have a conserved arginine in their act

18 Moreover, known methane-oxidizing enzymes have different expression levels, carb

19 levels for retinol, retinaldehyde, and ATRA-oxidizing enzymes; however, the contribution of retinald

20 The enzyme was the major formaldehyde-oxidizing enzyme in cells cultured in high (above 1 micr

21 al results of several flavin-dependent amine oxidizing enzymes including human monoamine oxidases A a

22 e from damage by intercepting the powerfully oxidizing enzyme intermediate (Compound I) and returning

23 To date, the best characterized choline-oxidizing enzyme is the flavin-dependent choline oxidase

24 he possible mechanistic pathways for sulfite-oxidizing enzymes is presented and related to available

25 found for HAO and HAO-related hydroxylamine-oxidizing enzyme kustc1061 from K. stuttgartiensis Inter

26 quitous tryptophan/tyrosine chains in highly oxidizing enzymes likely perform similar protective func

27 ttesting to its exceptional properties as an oxidizing enzyme mimic.

28 stutzeri WM88 encoding the novel phosphorus oxidizing enzyme NAD:phosphite oxidoreductase (trivial n

29 Powerfully oxidizing enzymes need protective mechanisms to prevent

30 A potent oxidizing enzyme of neutrophils, myeloperoxidase (MPO),

31 anic core (Mn(4)O(x)Ca(1)Cl(y)) of the water oxidizing enzyme of oxygenic photosynthesis generates O(

32 ) ligand bound to Mo as found in the sulfite oxidizing enzymes of the same family.

33 delivery of the gene for 15-lipoxygenase, an oxidizing enzyme present in atherosclerotic lesions.

34 it was uncertain whether NocL was the only N-oxidizing enzyme required for nocardicin A biosynthesis.

35 Sulfite oxidizing enzymes (SOEs) are molybdenum cofactor-depende

36 ation of sulfite is catalyzed by the sulfite-oxidizing enzymes (SOEs), which interact with an electro

37 troph growth and the activity of the methane-oxidizing enzyme soluble methane monooxygenase under con

38 ber of a recently recognized family of amine-oxidizing enzymes that all contain covalently bound flav

39 ssence is shared by another class of alcohol oxidizing enzymes that utilize a catalytic zinc to stabi

40 Nature's primary methane-oxidizing enzyme, the membrane-bound particulate methane

41 A broad-substrate-range xanthine-oxidizing enzyme was responsible for the formation of th

42 n and biochemical characterization of the Pt-oxidizing enzyme, which was proven to be BAP by N termin