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1 ex14-as well as the matrix proteins Pex8 and alcohol oxidase.
2 sa7 cells were unable to degrade peroxisomal alcohol oxidase.
3 ses, the 5' untranslated region (UTR) of the alcohol oxidase 1 (AOX1) gene is fused to the coding seq
4  than under control of the commonly employed alcohol oxidase 1 promoter (P(AOX1)) in methanol-grown c
5 n in Pichia pastoris under the regulation of alcohol oxidase 1 promoter.
6                                   SSPs, aryl-alcohol oxidases (AAO) and the intracellular aryl-alcoho
7           The bi-enzyme electrode is made of alcohol oxidase and horseradish peroxidase enzymes immob
8 stillation protocol, coupled with the use of alcohol oxidase and the formaldehyde-sensitive reagent P
9 methyl esters is oxidized to formaldehyde by alcohol oxidase, and the formaldehyde is continuously re
10 nol-induced pex mutants contain little or no alcohol oxidase (AOX) activity.
11                            We report here an alcohol oxidase (AOx) based third generation bioanode fo
12 ransducer, followed by the immobilization of alcohol oxidase (AOx) in an intermediate chitosan layer,
13                                              Alcohol oxidase (AOx) with a two-fold increase in effici
14                                              Alcohol oxidase (AOX), the first enzyme in the yeast met
15 n peroxide (H2O2) enzymatically generated by alcohol oxidase (AOx).
16             A simple one step method for the alcohol oxidases (AOx) protein mediated synthesis of gol
17 BBE-like 15 adopts the same fold as vanillyl alcohol oxidase as reported previously for berberine bri
18 on source results in high-level induction of alcohol oxidase expression.
19      K1B, were deficient in long-chain-fatty alcohol oxidase (FAO) activity.
20 ty acids by the sequential action of a fatty alcohol oxidase (FAO) and a fatty aldehyde dehydrogenase
21 bricated by immobilizing ferrocene entrapped alcohol oxidase (FcAOx) and sol-gel chitosan film coated
22 oup of a relatively new type of the vanillyl-alcohol oxidase flavoprotein family characterized by bic
23                        Unlike the intronless alcohol oxidases from methylotrophic yeasts, a genomic f
24                               The respective alcohol oxidase genes, AOX1 in Pp and MOX in Hp, have si
25         We have cloned and sequenced a novel alcohol oxidase (Hv-p68) from the filamentous fungus Hel
26                       The methanol-inducible alcohol oxidase I (AOXI) promoter of the methylotrophic
27 ble to those obtained with the commonly used alcohol oxidase I gene promoter (PAOX1).
28 some under control of the methanol inducible alcohol oxidase I promoter, resulting in a strain design
29                                              Alcohol oxidases, including carbohydrate oxidases, have
30 ased upon oxidation of ethanol by the enzyme alcohol oxidase obtained from the yeast Hansenula sp. wh
31 ignificant sequence identity (>67%) with the alcohol oxidases of the methylotrophic yeasts.
32           The anode consisted in immobilized alcohol oxidase on functionalized carbon nanotubes with
33 quence immediately downstream from the AOX1 (alcohol oxidase) promoter of Pichia pastoris, displacing
34 ulated of these genes is AOX1, which encodes alcohol oxidase, the first enzyme of the methanol pathwa
35 lysis to form methanol, which is consumed by alcohol oxidase to form formaldehyde while simultaneousl
36          One of the best-studied is vanillyl-alcohol oxidase (VAO) from the fungus Penicillium simpli
37 s Myceliophthora thermophila C1 for vanillyl-alcohol oxidase (VAO)-type flavoprotein oxidases, a puta

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