1.14.18.3	additional information	-	-	675831	
1.14.18.3	additional information	-	optimization of a coupled assay method with propylene as substrate and a duroquinol-based NADH regeneration system	672301	
1.14.18.3	0.003	-	using propylene as substrate, pH and temperature not specified in the publication	727340	
1.14.18.3	0.0053	-	using propylene as substrate, pH and temperature not specified in the publication	726954, 727340	
1.14.18.3	0.011	-	crude extract, using propylene as substrate, in 25 mM MOPS buffer (pH 7.0), at 30°C	716110	
1.14.18.3	0.011	-	purified enzyme form pMMO	438944	
1.14.18.3	0.012	-	purified enzyme, using propylene as substrate, in 25 mM MOPS buffer (pH 7.0), at 30°C	716110	
1.14.18.3	0.016	-	using propylene as substrate, pH and temperature not specified in the publication	727340	
1.14.18.3	0.0177	-	-	660351	
1.14.18.3	0.034	-	purified enzyme, substrates propylene and duroquinol	671965	
1.14.18.3	0.053	-	-	657810	
1.14.18.3	0.0605	-	whole cells, substrate formate	438944	
1.14.18.3	0.095	-	-	659033	
1.14.18.3	0.1037	-	at 45°C and pH 7.0, with NADH as cosubstrate, in the presence of bacteriohemerythrin	728079	
1.14.18.3	0.114	-	membrane-bound enzyme, substrates propylene and duroquinol	671965	
1.14.18.3	0.1228	-	at 45°C and pH 7.0, with duroquinol as cosubstrate, in the presence of bacteriohemerythrin	728079	
1.14.18.3	0.16	-	purified enzyme	687284	
1.14.18.3	0.23	-	membrane-bound enzyme, substrates propylene and NADH	671965