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MICROPLATE TURBIDIMETRIC ASSAY IN DETERMINING MILK-CLOTTING ACTIVITY OF ENZYME PREPARATIONS Microplate Turbidimetric Assay in Determining Milk-Clotting Activity of Enzyme Preparations

Published in Cheese- and buttermaking · Issue 3, 2026 · Pages 36–43 · Rubric: Original article
DOI: https://doi.org/10.21603/2073-4018-2026-3-67 · EDN: CYBVQE
Received: 13.04.2026 Accepted: 04.08.2026 Published: 09.09.2026 Language of publication: RUS
Milk-clotting activity (MCA) is a key quality indicator for enzymes used in cheese production. The traditional method for determining MCA (REMCAT) relies on visual detection of the clotting endpoint. Unfortunately, it is subjective and inefficient for analyzing large numbers of samples. Microplate turbidimetric methods can serve as an alternative, enabling objective and high-throughput MCA measurements. We analyzed the critical parameters governing the reaction (pH, buffer composition, temperature, calcium ion concentration, substrate concentration, and measurement wavelength) to select conditions for effective MCA determination. Our method is a simplified approach for determining the clotting time based on reaching a fixed optical density value. We tested the method using a recombinant chymosin preparation, CHY-MAX Extra. The experiment demonstrated a linear dependence of activity on enzyme concentration (R² > 0.98) in the range of 500–5,000 ng/ml. Calibration with a standard milk-clotting enzyme reference made it possible to express the results in conventional units. The method enables quantitative assessment of total MCA with minimal consumption of enzyme and substrate. The new protocol represents an effective tool for high-throughput screening of novel recombinant and natural milk-clotting enzymes, providing rapid analysis and straightforward data processing.
chymosin, milk-clotting activity, microplate turbidimetric assay, cheesemaking
Funding
The work was carried out as part of fulfilling the state assignment of the National Research Center “Kurchatov Institute”.
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1. Juste, E. Milk gel formation and properties: impact of whey protein aggregates / E. Juste, J. Lee, T. Croguennec // International Dairy Journal. 2025. Vol. 169. Art. no. 106354. https://doi.org/10.1016/j.idairyj.2025.106354

2. Kübarsepp, I. A comparison of the methods for determination of the rennet coagulation properties of milk / I. Kübarsepp [et al.] // Acta Agriculturae Scandinavica, Section A — Animal Science. 2005. Vol. 55(4). P. 145–148. https://doi.org/10.1080/09064700500453377

3. Caeiro, J. J. Comparison of milk-clotting activity measurement using the Berridge’s operator-based approach and a proposed digital method / J. J. Caeiro [et al.] // International Dairy Journal. 2024. Vol. 159. Art. no. 106055. https://doi.org/10.1016/j.idairyj.2024.106055

4. Loddo, A. Detecting coagulation time in cheese making by means of computer vision and machine learning techniques / A. Loddo [et al.] // Computers in Industry. 2025. Vol. 164. Art. no. 104173. https://doi.org/10.1016/j.compind.2024.104173

5. You, H. Ratiometric fluorescent detection of protease activity in foods based on microwave-assisted synthesized casein-directed gold nanoclusters / H. You [et al.] // Food Chemistry. 2025. Vol. 474. Art. no. 143078. https://doi.org/10.1016/j.foodchem.2025.143078

6. Ben Amira, A. Milk-clotting properties of plant rennets and their enzymatic, rheological, and sensory role in cheese making: a review / A. Ben Amira [et al.] // International Journal of Food Properties. 2017. Vol. 20(sup1). P. S76–S93. https://doi.org/10.1080/10942912.2017.1289959

7. Jensen, J. L. The function of the milk-clotting enzymes bovine and camel chymosin studied by a fluorescence resonance energy transfer assay / J. L. Jensen [et al.] // Journal of Dairy Science. 2015. Vol. 98(5). P. 2853–2860. https://doi.org/10.3168/jds.2014-8672

8. Lu, X. A novel fluorescence sensor for milk clotting enzyme chymosin using peptide as substrate and covalent organic framework nanosheet as fluorescence quencher / X. Lu [et al.] // Food Science and Human Wellness. 2024. Vol. 13(6). P. 3606–3613. https://doi.org/10.26599/FSHW.2023.9250042

9. Wiśniewski, P. Invited review: Milk-clotting enzymes of microbial origin and their role in cheesemaking–A review / P. Wiśniewski [et al.] // Journal of Dairy Science. 2025. Vol. 108(10). P. 10427–10446. https://doi.org/10.3168/jds.2025-26973

10. Arbita, A. A. Milk clotting enzymes from marine resources and their role in cheese-making: a mini review / A. A. Arbita, J. Zhao // Critical Reviews in Food Science and Nutrition. 2024. Vol. 64(27). P. 10036–10047. https://doi.org/10.1080/10408398.2023.2220030

11. Nicosia, F. D. Plant milk-clotting enzymes for cheesemaking / F. D. Nicosia [et al.] // Foods. 2022. Vol. 11(6). Art. no. 871. https://doi.org/10.3390/foods11060871

12. Akishev, Z. Obtaining of recombinant camel chymosin and testing its milk-clotting activity on cow’s, goat’s, ewes’, camel’s and mare’s milk / Z. Akishev [et al.] // Biology. 2022. Vol. 11(11). Art. no. 1545. https://doi.org/10.3390/biology11111545

13. Kappeler, S. R. Characterization of recombinant camel chymosin reveals superior properties for the coagulation of bovine and camel milk / S. R. Kappeler [et al.] // Biochemical and Biophysical Research Communications. 2006. Vol. 342(2). P. 647–654. https://doi.org/10.1016/j.bbrc.2006.02.014

14. Jiang, X. P. Constitutive expression, purification and characterization of bovine prochymosin in Pichia pastoris GS115 / X. P. Jiang [et al.] // World Journal of Microbiology and Biotechnology. 2012. Vol. 28(5). P. 2087–2093. https://doi.org/10.1007/s11274-012-1012-7

15. Ali Hanoğlu, S. Recombinant expression and characterization of Oryctolagus cuniculus chymosin in Komagataella phaffii (Pichia pastoris) / S. Ali Hanoğlu, D. Ektiren, M. Karaaslan // Protein Expression and Purification. 2021. Vol. 183. Art. no. 105874. https://doi.org/10.1016/j.pep.2021.105874

16. Vallejo, J. A. Cloning and expression of buffalo active chymosin in Pichia pastoris / J. A. Vallejo [et al.] // Journal of Agricultural and Food Chemistry. 2008. Vol. 56(22). P. 10606–10610. https://doi.org/10.1021/jf802339e

17. Dunn-Coleman, N. S. Commercial levels of chymosin production by Aspergillus / N. S. Dunn-Coleman [et al.] // Biotechnology. 1991. Vol. 9(10). P. 976–981. https://doi.org/10.1038/nbt1091-976

18. Gilliland, G. L. Functional implications of the three-dimensional structure of bovine chymosin / G. L. Gilliland, M. T. Oliva, J. Dill // Advances in Experimental Medicine and Biology. 1991. Vol. 306. P. 23–37. https://doi.org/10.1007/978-1-4684-6012-4_3

19. Zhang, Y. Quantifying protein residues in APIs: Bradford assay mechanism and limitations, outperformed by HILIC-MS/MS / Y. Zhang [et al.] // Journal of Pharmaceutical Analysis. 2026. Vol. 16(7). Art. no. 101552. https://doi.org/10.1016/j.jpha.2026.101552

20. Akishev, Z. Constitutive expression of Camelus bactrianus prochymosin B in Pichia pastoris / Z. Akishev [et al.] // Heliyon. 2021. Vol. 7(5). Art. no. e07137. https://doi.org/10.1016/j.heliyon.2021.e07137

21. Wang, N. Expression and characterization of camel chymosin in Pichia pastoris / N. Wang [et al.] // Protein Expression and Purification. 2015. Vol. 111. P. 75–81. https://doi.org/10.1016/j.pep.2015.03.012

22. Nájera, A. I. Effects of pH, temperature, CaCl2 and enzyme concentrations on the rennet-clotting properties of milk: a multifactorial study / A. I. Nájera, M. de Renobales, L. J. R. Barron // Food Chemistry. 2003. Vol. 80(3). P. 345–352. https://doi.org/10.1016/S0308-8146(02)00270-4

23. Nicolau, N. Estimation of clotting and cutting times in sheep cheese manufacture using NIR light backscatter / N. Nicolau [et al.] // Dairy Science & Technology. 2015. Vol. 95. P. 495–507. https://doi.org/10.1007/s13594-015-0232-7

24. Tabayehnejad, N. Comparison of total milk-clotting activity measurement precision using the Berridge clotting time method and a proposed optical method / N. Tabayehnejad, M. Castillo, F. A. Payne // Journal of Food Engineering. 2012. Vol. 108(4). P. 549–556. https://doi.org/10.1016/j.jfoodeng.2011.09.009

25. Castillo, M. Z. Modelling casein aggregation and curd firming in goats’ milk from backscatter of infrared light / M. Z. Castillo [et al.] // Journal of Dairy Research. 2003. Vol. 70(3). P. 335–348. https://doi.org/10.1017/S0022029903006356

26. Pushkarev, V. A. Molokosvertyvayuschaya i obschaya proteoliticheskaya aktivnost' inzhenernogo varianta rekombinantnogo himozina severnogo olenya (Rangifer tarandus) / V. A. Pushkarev [i dr.] // Syrodelie i maslodelie. 2023. № 1. S. 22–25. https://doi.org/10.31515/2073-4018-2023-1-22-25; https://elibrary.ru/uarlkp