Pasteurella damsela α2-6 Sialyltransferase A200Y/S232Y
Abbreviation
Pd26ST-A200Y/S232Y
Source
Pasteurella damsela
Activity
Transfer Sia via an α2-6 linkage
Expression
&
Purification
Expression system: pET15b with N-terminal His6-tag , E. coli BL21(DE3)
Induction condition: 0.1 mM IPTG, 37 °C, 3 h, 250 rpm, Luria LB broth
Purification:
1) Suspend cells in ice-cold 40 mL Buffer-A + 0.1% Trixon X100
2) Disrupt cells by a CF1 cell disruptor (Constant Systems), 20 kPsi, 4 °C
3) Centrifuge at 12000 x g, 4 °C, 30 min
4) Load supernatant to a 10 mL gravity column filled with 2 mL Ni-NTA resin (pre-equilibrated)
5) Wash with 50 mL Buffer-A, then 50 mM Buffer-B, finally elute with 10 mL Buffer-C.
6) Concentrate into 2.5 mL and change buffer to Buffer D using a PD-10 column.
7) Store at -20 °C for up to 6 months
Buffers: A: 20 mM Tris-HCl (pH 8.0), 300 mM NaCl, 10 mM imidazole;
B: A + 15 mM imidazole; C: A + 250 mM imidazole.
D: 50 mM Tris-HCl (pH 8.0), 100 mM NaCl, 50 % Glycerol
Optimal Condition
37 °C
8.5
MgCl2
50 mM Tris-HCl (pH 8.5), 22 mM donor, 20 mM acceptor, 20 mM MgCl2, incubate at 37 °C for 30 min.
Temperature:
pH:
Metal ion:
Example condition:
CMP-Neu5Ac/Neu5Gc/Kdn
Terminal Gal/GalNAc
Donor:
Acceptor:
Kinetic:
Substrate Specificity
-
Xu, Y.; Fan, Y.; Ye, J.; Wang, F.; Nie, Q.; Wang, L.; Wang, P. G.; Cao, H.; Cheng, J., Successfully Engineering a Bacterial Sialyltransferase for Regioselective α2,6-sialylation. ACS Catalysis 2018, 8 (8), 7222-7227.
References