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

Table 6.

Yields (η) obtained in the kinetically controlled synthesis of Z-Tyr-Val-OH in ethyl ethanoate (Xw: 1 × 10−5 in the enzyme into the organic solvent) at 40°C, using glyoxyl-silica immobilized antiacanthain (12.5 mg/ml) as biocatalyst.

Time (min) Z- Tyr-pNO (mM) Z-Tyr-Val-OH (mM) αs (%) η (%)
0 17.25 0 0a 0a
5 14.83 2.41 14 ± 0.20b 14 ± 0.00b
15 12.94 4.30 25 ± 0.37c 25 ± 0.01c
30 10.35 6.90 40 ± 0.00d 40 ± 0.15d
60 9.15 8.20 47 ± 0.10e 47± 0.03e
240 4.80 12.10 72 ± 0.00f 70 ± 0.02f
360 4.25 12.94 75 ± 0.18g 75 ± 0.13g

αs is the conversion percentage of acyl donor substrate.

The values with different superscript letters in a column are significantly different (p < 0.05) (IBM SPSS Statistics 27.0).

Bold values represent the maximal peptide yields from each experimental trial set.