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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
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
12 ransducer, followed by the immobilization of alcohol oxidase (AOx) in an intermediate chitosan layer,
17 BBE-like 15 adopts the same fold as vanillyl alcohol oxidase as reported previously for berberine bri
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
28 some under control of the methanol inducible alcohol oxidase I promoter, resulting in a strain design
30 ased upon oxidation of ethanol by the enzyme alcohol oxidase obtained from the yeast Hansenula sp. wh
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
37 s Myceliophthora thermophila C1 for vanillyl-alcohol oxidase (VAO)-type flavoprotein oxidases, a puta
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