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HRID 380166作成日:2026年10月27日

NADPH → 4-Hydroxybenzaldehyde

https://huagongshe.com/reaction/380166

反応式

関与物質

役割名称HCID仕込み量
反応物NADPHHCID 5884—
反応物TricineHCID 79784—
反応物(4-Hydroxyphenyl)acetaldehyde oximeHCID 152653—
生成物4-HydroxybenzaldehydeHCID 126—

反応手順

5 μl membranes isolated as described in Halkier et al, Archives of Biochemistry and Biophysics 322: 369-377, 1995, from E. coli expressing “12” was reconstituted with 0.225 units NADPH-cytochrome P450-reductase, 50 μg NADPH, 42 nCi p-hydroxyphenylacetaldehyde oxime, and 100 μg dilaurylphosphatidylcholine in a total volume of 100 μl of 30 mM Tricine pH 7.9. After incubation at 30° C. for 30 minutes the reaction mixture was applied to a TLC plate and analyzed as described above. Reconstitution of membranes from E. coli expressing “12” resulted in the accumulation of p-hydroxybenzaldehyde which is the stable dissociation product of p-hydroxymandelonitrile, the last intermediate in the biosynthesis of the cyanogenic glucoside dhurrin. This shows that demonstrates that “12” is the cytochrome P450 that catalyzes the conversion of p-hydroxyphenylacetaldehyde oxime to p-hydroxymandelonitrile. The cDNA is designated P450OX. A clone comprising the described cDNA of P450OX has been deposited on Jan. 10, 1997 with the DSMZ-Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH, Mascheroder Weg 1b, D-38124 Braunschweig, under the accession number DSM 11367.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06300544B1
出典データセットuspto-grants-2001_10
ORD IDord-21ac1516ddd141008844e67fa55522ce
出典メモuspto-grants-2001_10