Table 3.
Entry |
Substr. |
Variant |
Conv. [%] |
||
---|---|---|---|---|---|
air |
O2 (2 bar) |
O2 (4 bar) |
|||
1 |
1 a |
wt |
16 |
13 |
10 |
2 |
1 a |
V465T |
50 |
31 |
26 |
3 |
1 a |
V465 S |
50 |
35 |
26 |
4 |
1 a |
V465T/W466H |
25 |
18 |
9 |
5 |
1 a |
V367R/W466F |
18 |
9 |
7 |
6 |
2 a |
wt |
29 |
33 |
35 |
7 |
2 a |
V465T |
50 |
48 |
45 |
8 |
2 a |
V465 S |
50 |
48 |
44 |
9 |
2 a |
V465T/W466H |
50 |
48 |
46 |
10 |
2 a |
V367R/ W466F |
33 |
34 |
46 |
[a] Condition: KPi‐buffer (200 mM, pH 7.0) containing the oxidases (14.2 μM final concentration in 500 μL reaction volume in 4 mL glass vials), catalase from Micrococcus lysodeikticus (15 μL, 170000 U/mL), 1 a–2 a (50 mM). The reaction mixtures were shaken for 16 hours (170 rpm, 21 °C) and extracted with ethyl acetate (2×300 μL), dried with Na2SO4 and analyzed by GC‐FID. Conversions were measured based on area ratio of ketone to substrate. Reactions were done in duplicate.