1.1.1.71	(RS)-1-phenylethanol + NAD+	100% activity	
1.1.1.71	(RS)-1-phenylethanol + NADP+	100% activity	
1.1.1.71	1-(2-bromophenyl)ethanol + NAD(P)+	11.3% activity compared to (RS)-1-phenylethanol	
1.1.1.71	1-(2-chlorophenyl)ethanol + NAD(P)+	16.4% activity compared to (RS)-1-phenylethanol	
1.1.1.71	1-(3-bromophenyl)ethanol + NAD(P)+	315% activity compared to (RS)-1-phenylethanol	
1.1.1.71	1-(3-chlorophenyl)ethanol + NAD(P)+	205% activity compared to (RS)-1-phenylethanol	
1.1.1.71	1-(4-bromophenyl)ethanol + NAD(P)+	167% activity compared to (RS)-1-phenylethanol	
1.1.1.71	1-(4-chlorophenyl)ethanone + NAD(P)+	151% activity compared to (RS)-1-phenylethanol	
1.1.1.71	1-(4-fluorophenyl)ethanol + NAD(P)+	119% activity compared to (RS)-1-phenylethanol	
1.1.1.71	1-(4-methylphenyl)ethanone + NAD(P)+	189% activity compared to (RS)-1-phenylethanol	
1.1.1.71	1-butanol + NAD(P)+	2.3% activity compared to (RS)-1-phenylethanol	
1.1.1.71	1-heptanol + NAD(P)+	3.3% activity compared to (RS)-1-phenylethanol	
1.1.1.71	1-hexanol + NAD(P)+	2.8% activity compared to (RS)-1-phenylethanol	
1.1.1.71	1-octanol + NAD(P)+	2.3% activity compared to (RS)-1-phenylethanol	
1.1.1.71	1-pentanol + NAD(P)+	2.8% activity compared to (RS)-1-phenylethanol	
1.1.1.71	1-phenyl-1,2-ethanediol + NAD(P)+	3.4% activity compared to (RS)-1-phenylethanol	
1.1.1.71	1-phenyl-1-propanol + NAD(P)+	13.1% activity compared to (RS)-1-phenylethanol	
1.1.1.71	1-phenyl-2-propanol + NAD(P)+	39.1% activity compared to (RS)-1-phenylethanol	
1.1.1.71	1-propanol + NAD(P)+	1.2% activity compared to (RS)-1-phenylethanol	
1.1.1.71	2,2,2-trifluoroacetophenone + NAD(P)H + H+	180% activity compared to acetoin	
1.1.1.71	2-bromoacetophenone + NAD(P)H + H+	8.7% activity compared to acetoin	
1.1.1.71	2-butanol + NAD(P)+	22.3% activity compared to (RS)-1-phenylethanol	
1.1.1.71	2-chloro-1-phenylethanol + NAD(P)+	0.3% activity compared to (RS)-1-phenylethanol	
1.1.1.71	2-heptanol + NAD(P)+	61.6% activity compared to (RS)-1-phenylethanol	
1.1.1.71	2-hexanol + NAD(P)+	38.7% activity compared to (RS)-1-phenylethanol	
1.1.1.71	2-hexanone + NAD(P)H + H+	3.6% activity compared to acetoin	
1.1.1.71	2-octanol + NAD(P)+	45.8% activity compared to (RS)-1-phenylethanol	
1.1.1.71	2-pentanol + NAD(P)+	30.2% activity compared to (RS)-1-phenylethanol	
1.1.1.71	2-phenylethanol + NAD(P)+	0.3% activity compared to (RS)-1-phenylethanol	
1.1.1.71	2-propanol + NAD(P)+	5.3% activity compared to (RS)-1-phenylethanol	
1.1.1.71	acetoin + NAD(P)+	100% activity	
1.1.1.71	acetoin + NAD(P)H + H+	4.5% activity compared to (RS)-1-phenylethanol	
1.1.1.71	acetone + NAD(P)H + H+	4.1% activity compared to acetoin	
1.1.1.71	all-trans-retinal + NADPH + H+	-	
1.1.1.71	cyclohexanol + NAD(P)+	52.3% activity compared to (RS)-1-phenylethanol	
1.1.1.71	cyclohexanone + NAD(P)H + H+	19.1% activity compared to acetoin	
1.1.1.71	D-arabinose + NAD(P)+	21.4% activity compared to (RS)-1-phenylethanol	
1.1.1.71	dihydroxyacetone + NAD(P)H + H+	34.8% activity compared to acetoin	
1.1.1.71	ethanol + NAD(P)+	0.5% activity compared to (RS)-1-phenylethanol	
1.1.1.71	ethyl pyruvate + NAD(P)H + H+	294% activity compared to acetoin	
1.1.1.71	hexanal + NAD(P)H + H+	12.9% activity compared to acetoin	
1.1.1.71	L-arabinose + NAD(P)+	5.2% activity compared to (RS)-1-phenylethanol	
1.1.1.71	meso-2,3-butanediol + NAD+	272% activity compared to (RS)-1-phenylethanol	
1.1.1.71	meso-2,3-butanediol + NADP+	272% activity compared to (RS)-1-phenylethanol	
1.1.1.71	methanol + NAD(P)+	0.2% activity compared to (RS)-1-phenylethanol	
1.1.1.71	methyl benzoylformate + NAD(P)H + H+	67% activity compared to acetoin	
1.1.1.71	additional information	the enzyme plays an important role in potato defence response to Erwinia carotovora	
1.1.1.71	additional information	no activity with D-arabinose, L-arabinose, acetophenone, and 4-chloroacetophenone	
1.1.1.71	phenylacetaldehyde + NAD(P)H + H+	18.6% activity compared to acetoin	
1.1.1.71	pyruvic aldehyde + NAD(P)H + H+	328% activity compared to acetoin	
1.1.1.71	retinaldehyde + NADH	the enzyme is involved in retinol and vitamin A metabolism, retinoic acid is important in intestinal epithelial cell proliferation and differentiation, the enzyme also plays a role in dietary conversion of beta-carotene to retinol via retinaldehyde