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. 2020 Jul 22;8:707. doi: 10.3389/fbioe.2020.00707

Table 3.

Amine substrate scope (10 mM scale) of wild-type TsRTAa.

graphic file with name fbioe-08-00707-i0022.jpg
Substrate Conversion (%)
after 30 min after 24 h
(R)-Methylbenzylamined graphic file with name fbioe-08-00707-i0023.jpg 75 ± 1 96 ± 1
(S)-Methylbenzylamineb graphic file with name fbioe-08-00707-i0024.jpg <0.5 <0.5
(±)-Methylbenzylaminebc graphic file with name fbioe-08-00707-i0025.jpg 82 ± 3 94 ± 1
L-Alanine graphic file with name fbioe-08-00707-i0026.jpg n.d. n.d.
D-Alanine graphic file with name fbioe-08-00707-i0027.jpg 29 ± 4 30 ± 4
(±)-Alaninec graphic file with name fbioe-08-00707-i0028.jpg 30 ± 4 31 ± 4
β-Alanine graphic file with name fbioe-08-00707-i0029.jpg 6 ± 5 12 ± 4
Isopropylamine graphic file with name fbioe-08-00707-i0030.jpg 28 ± 4 88 ± 4
Cadaverine graphic file with name fbioe-08-00707-i0031.jpg 23 ± 4 44 ± 3
o-Xylylenediamine graphic file with name fbioe-08-00707-i0032.jpg n.d. 7 ± 5
p-Nitrophenethylamine graphic file with name fbioe-08-00707-i0033.jpg 23 ± 4 53 ± 6
a

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).

b

10 mM pyruvate.

c

20 Mm.

“ < 0.5” = calculated conversion smaller than uncertainty from calibration curve. “n.d.” = no product detected.