. 2021 Jun 28;8:685330. doi: 10.3389/fnut.2021.685330

Table 1.

Catalytic potential of soluble antiacanthain (0.075 mg/ml, 1.875 IU/ml) after 6 h in liquid-liquid biphasic systems constituted by several concentrations of organic solvent in 100 mM Tris(hydroxymethyl)amino methane hydrochloride buffer pH 8, at 40°C.

Organic solvent	Catalytic potential (IU/mg · h)^*
	30%	50%	70%
Benzene	140.70 ± 0.01^h	125.33 ± 0.19^f	121.75 ± 0.05^g
Octanol	114.19 ± 0.25^e	108.03 ± 0.05^c	78.33 ± 0.01^b
Dichloromethane	123.64 ± 0.01^f	116.77 ± 0.05^d	104.39 ± 0.10^d
Diethyl ether	97.68 ± 0.05^c	93.07 ± 0.09^b	116.71 ± 0.34^e
Cyclohexane	134.71 ± 0.05^g	147.19 ± 0.01^g	120.82 ± 0.05^f
Chlorobenzene	68.76 ± 0.23^a	123.57 ± 0.01^e	56.50 ± 0.02^a
Acetophenone	85.57 ± 0.01^b	89.22 ± 0.01^a	83.24 ± 0.01^c
Ethyl ethanoate	104.97 ± 0.15^d	170.62 ± 0.01^h	126.40 ± 0.01^h

The catalytic potential of antiacanthain in 100 mM Tris(hydroxymethyl)amino methane hydrochloride buffer pH 8, at 40°C was 116.48 ± 0.01 (IU/mg · h).

Catalytic potential data are expressed as the mean ± SD (standard deviation) of three independent experiments which were done in duplicate. The values with different superscript letters in a column are significantly different (p < 0.05) (IBM SPSS Statistics 27.0).