Table 3.
Amine substrate scope (10 mM scale) of wild-type TsRTAa.
![]() | |||
---|---|---|---|
Substrate | Conversion (%) | ||
after 30 min | after 24 h | ||
(R)-Methylbenzylamined | ![]() |
75 ± 1 | 96 ± 1 |
(S)-Methylbenzylamineb | ![]() |
<0.5 | <0.5 |
(±)-Methylbenzylaminebc | ![]() |
82 ± 3 | 94 ± 1 |
L-Alanine | ![]() |
n.d. | n.d. |
D-Alanine | ![]() |
29 ± 4 | 30 ± 4 |
(±)-Alaninec | ![]() |
30 ± 4 | 31 ± 4 |
β-Alanine | ![]() |
6 ± 5 | 12 ± 4 |
Isopropylamine | ![]() |
28 ± 4 | 88 ± 4 |
Cadaverine | ![]() |
23 ± 4 | 44 ± 3 |
o-Xylylenediamine | ![]() |
n.d. | 7 ± 5 |
p-Nitrophenethylamine | ![]() |
23 ± 4 | 53 ± 6 |
Unless otherwise stated, 10 mM benzaldehyde was used as the carbonyl acceptor. Conversions are based on the formation of either acetophenone or benzylamine, as determined by HPLC and calculated from a calibration curve. All reactions were carried out in triplicate. Standard errors include the SE of the calibration curve. (Ellison and Williams, 2012; Theodorou et al., 2012).
10 mM pyruvate.
20 Mm.
“ < 0.5” = calculated conversion smaller than uncertainty from calibration curve. “n.d.” = no product detected.