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. 2015 Mar 25;5(2):37–43. doi: 10.1016/j.ijpddr.2015.03.001

Table 1.

Activity of recombinant G. lamblia nitroreductases (GlNR1 and GlNR2) with various nitro- and non-nitro compounds (0.1 mM) as substrates. Functional assays were performed with MTT as chromogenic electron acceptor. Electron donor was NADH or NADPH if specified. The reaction was performed at 37 °C and stopped after various time points by addition of one volume pure ethanol. Mean values (±SE) are given for three replicates after subtraction of enzyme and substrate blanks.

Substrate GlNR1 GlNR2
(ΔA590 min−1 mg prot−1)
Menadione 22.9 ± 0.4 16.2 ± 0.2
Menadione NADPH 1.8 ± 0.2 0.2 ± 0.1
Dicoumarol 3.1 ± 0.2 0.8 ± 0.1
Menadione + dicoumarol 27.2 ± 0.3 14.5 ± 0.1
Ubiquinone (coenzyme Q10) 2.8 ± 0.1 1.8 ± 0.2
FAD 11.8 ± 0.4 8.9 ± 0.9
Dinitrotoluene 5.2 ± 0.3 2.8 ± 0.2
Dinitrotoluene NADPH 0.9 ± 0.3 0.3 ± 0.1
7-Nitrocoumarine 10.6 ± 0.3 6.5 ± 0.5
Dinitrophenol 5.9 ± 0.4 0.2 ± 0.1
Nitrophenol 2.9 ± 0.1 2.6 ± 0.1
Metronidazole 2.8 ± 0.2 1.7 ± 0.1
Nitazoxanide 2.7 ± 0.2 1.9 ± 0.1
CB1954 3.0 ± 0.1 1.7 ± 0.1
C17 2.1 ± 0.2 0.9 ± 0.1