Purification and Characterization of a Small Thermostable Protease from Streptomyces sp. CNXK100
28 kwi 2024
O artykule
Kategoria artykułu: Original Paper
Data publikacji: 28 kwi 2024
Zakres stron: 155 - 165
Otrzymano: 16 gru 2023
Przyjęty: 13 mar 2024
DOI: https://doi.org/10.33073/pjm-2024-014
Słowa kluczowe
© 2024 Tan Viet Pham et al., published by Sciendo
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

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Effect of various chemicals on CNXK100 thermostable protease activity_
Group | Chemical | Concentration | Residual activity (%) |
---|---|---|---|
Control | – | – | 100.00 |
Organic solvents | Methanol | 10.0% | 89.28 ± 3.63 |
Ethanol | 86.54 ± 2.36 | ||
Isopropanol | 79.47 ± 1.85 | ||
Butanol | 43.93 ± 2.32 | ||
Chloroform | 86.54 ± 2.34 | ||
Surfactants | Triton X-100 | 1.0% | 101.27 ± 2.58 |
Tween 20 | 88.13 ± 1.93 | ||
Tween 80 | 92.06 ± 3.21 | ||
SDS | 53.42 ± 3.05 | ||
Bleaching agents | NaClO | 0.5% | 105.86 ± 0.57 |
1.0% | 111.36 ± 0.86 | ||
1.5% | 113.17 ± 1.62 | ||
2.0% | 114.11 ± 0.53 | ||
2.5% | 121.47 ± 2.28 | ||
3.0% | 120.75 ± 1.34 | ||
H2O2 | 0.5% | 89.21 ± 2.03 | |
1.0% | 77.85 ± 9.51 | ||
1.5% | 74.12 ± 10.34 | ||
2.0% | 71.68 ± 12.29 | ||
2.5% | 75.51 ± 2.12 | ||
3.0% | 66.96 ± 13.07 | ||
Proteolytic enzymes | Pepsin | 0.1 mg/ml | 101.54 ± 1.43 |
Trypsin | 68.97 ± 0.51 | ||
Chymotrypsin | 91.34 ± 0.13 | ||
Proteinase K | 10.80 ± 0.44 |
Purification of thermostable protease from Streptomyces sp_ CNXK100_
Purification steps | Total protein (mg) | Total activity (U) | Specific activity (U/mg) | Activity recovery (%) | Purification level |
---|---|---|---|---|---|
Crude extract | 54.64 | 1.14 x 106 | 2.09 x 104 | 100.00 | 1.00 |
Heat-treatment | 18.62 | 4.14 x 105 | 2.22 x 104 | 36.32 | 1.06 |
Fractional precipitation with 60% (NH4)2SO4 | 0.81 | 1.95 x 105 | 2.41 x 105 | 17.11 | 11.53 |
Gel filtration | 0.011 | 2.63 x 104 | 2.40 x 106 | 2.31 | 114.83 |