Neisseria meningitidis b1-4 galactosyltransferase
Abbreviation
NmLgtB
Source
Neisseria meningitidis
Activity
Transfer Gal from UDP-Gal to GlcNAc via a b1,4-linkage
Expression
&
Purification
Expression system: pET15b with N-terminal His6-Tag , E. coli BL21(DE3)
Induction condition: 0. 2 mM IPTG, 16 °C, 20 h, 200 rpm, Luria LB broth
Purification: >30 mg/L culture
1) Suspend cells collected from 1 L medium in ice-cold 40 mL Buffer-A
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 4 °C for up to 6 months, store at -80 °C for up to 1 year (avoid repeated freeze)
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, 20 % Glycerol
Optimal Condition
37 °C
5.0-6.5
MnCl2, MgCl2
50 mM MES-KOH (pH 6.0), 22 mM donor, 20 mM acceptor, 20 mM MnCl2, incubate at 37 °C for 1 h to overnight.
Temperature:
pH:
Metal ion:
Example condition:
UDP-Gal
GlcNAc/Glc, tolerate modifications at C2 position, dose not tolerate modifications at C6 position
Donor:
Acceptor:
Kinetics:
Substrate Specificity
-
Lau K., Thon V., et al. Highly efficient chemoenzymatic synthesis of b1–4-linked galactosides with promiscuous bacterial b1–4-galactosyltransferasesw. ChemComm, 2010, 46, 6066.
References