ФЕНОМЕНОЛОГИЧЕСКАЯ МОДЕЛЬ КОАГУЛЯЦИИ МОЛОКА
Аннотация и ключевые слова
Аннотация (русский):
Предложена модель дополнительной стабилизации коллоидной системы молока за счет возникновения электрического заряда мицелл при диссоциации мицеллярного казеината кальция. Модель позволяет понять уникальность роли кальция при свертывании молока, описать особенности температурной зависимости коагуляции, а также в рамках единых представлений объяснить природу сычужной, кислотной, термокислотной и термокальциевой коагуляции.

Ключевые слова:
коагуляция молока, казеинат кальция, коллоидный фосфат кальция, ионизированный кальций
Текст

INTRODUCTION

Milk clotting is one of important technological processes in the manufacturing of many foodstuffs, in particular, cheeses. This process is based on the coagulation of casein micelles, which may be caused by various factors, such as enzymes, acids, spirits, salts, or high temperature [1].

It is recognized now that the colloid stability of casein micelles in milk is ensured, basically, by the presence of the -casein macropeptide hairy layer on the casein micelle surface, sterically restricting the possible clinging together of micelles [2--5]. In essence, this layer represents a quasielastic polyelectric brush formed by negatively charged macropeptide residues [6, 7].

The loss of colloid stability by the casein micellar system may be attributed to different ways of the destruction of the hairy layer. Therefore, under rennet conditions, -casein macropeptide hairs are split off by chymosin, which leads to the destruction of the protective layer. During acid coagulation, additional hydrogen ions easily get into the polyelectric brush and shift ion equilibrium to the recombination of dissociated -casein macropeptide acid groups, thus reducing the electric charge of macropeptide hairs and finally collapsing the protective layer [8].

Certain distinctions in mechanisms of the destruction of the casein micelle protective layer, as well as a number of factors affecting the micellar casein system's colloid stability, make it very difficult to describe various kinds of milk coagulation with a uniform approach. For example, it is known that the lack of calcium in milk has no significant effect on acid milk coagulation, while it is impossible to coagulate this milk by adding chymosin even after it has completely cut off the protective hairy layer [9, 10].

This research is an attempt to work out a universal model of milk coagulation, which would correctly describe, at least qualitatively, observable features of the milk coagulation phenomenon under various conditions of casein colloid system destabilization.

The background of our model is represented by both well-known experimentally confirmed facts and somehow substantiated but still hypothetical assumptions. In particular, the basic hypothesis rests on the analysis of the outstanding role of calcium ions in the stabilization of the micellar colloid systems in milk.

We hope that this paper will become a stimulus for the direct experimental check of our hypotheses by interested experimentalists.

MATERIALS AND METHODS

Skim milk was reconstituted by mixing up 90 g of low-fat milk powder (Milk Factory, Kemerovo, Russia) with 910 ml of distilled water and 4 cm3 of 10% solution of calcium chloride. Then, after complete dissolution, the reconstituted milk was left for about 12 hours at 6 ± 2ºС.

Milk coagulation was carried out in a thermostatted 200 ml cell.

The chymosin under the trademark of Maxiren® (DSM, Netherlands) was used for rennet coagulation. To prepare the enzyme solution, 0.1 g of dry Maxiren® powder was dissolved in 100 cm3 of distilled water.

For simulating acid coagulation, a 10% lactic acid solution (Univerkhim, Chelyabinsk, Russia) was slowly brought to milk under careful mixing.

To increase the pH of some milk samples, a 0.5-mM sodium hydroxide solution (NaOH) (Univerkhim, Chelyabinsk, Russia) was used.

Soluble calcium was added to milk in the form of 10% CaCl2 medical solution (Shenlu Pharm, China).

To decrease calcium ion concentration in milk, in a number of experiments Trilon B® (Na2EDTA) (Khimservis, Ufa, Russia) was used as a chelating agent.

Calcium ion concentration and pH in milk were measured with ELIT (Niko-Analit, Moscow, Russia) ion selective electrodes.

The casein micelles -potential was measured by means of Zetasizer Nano Z - ZEN2600 (Malvern Instruments, Malvern, UK).

Milk coagulation was monitored with a computer-driven "thermometric" gauge of our own design [11]. This device measures temperature difference between two thermocouple junctions immersed in milk at a distance of about 3 cm from each other. One of the junctions is attached directly to a small resistor dissipating permanently about 0.5 W of heat. An increase in milk viscosity during coagulation leads to an increase in temperature difference. It is more correct to say that the temperature increase near the warmed-up junction is due not only to the viscosity increase but also to the formation of a gel net structure, which also restricts convection in milk. In a sense, our method is similar to the hot wire method [12]. Hereinafter, the curves obtained by means of the thermometric gauge are called thermograms (by analogy with rheograms).

Список литературы

1. Fox, P.F., Guinee, T.P., Cogan, T.M., and McSweeney, P.L.H., Fundamentals of Cheese Science, Aspen, 2000.

2. Dalgleish, D.G., Casein micelles as colloids: Surface structure and stabilities, Journal of Dairy Science, 1998, vol. 81, pp. 3013--3017.

3. Horne, D.S., Casein structure, self-assembly, and gelation, Current Opinion in Colloid and Interface Science, 2002, vol. 7, pp. 456--461.

4. Dalgleish, D.G., On the structural models of bovine casein micelles - review and possible improvements, Soft Matter, 2011, vol. 7, pp. 2265--2272.

5. De Kruif, C.G., Huppertz, T., Urban, V.S., and Petukhov, A.V., Casein micelles and their internal structure, Advances in Colloid and Interface Science, 2012, vols. 171-172, pp. 36-52.

6. De Kruif, C.G. and Zhulina, E.B., κ-Casein as a polyelectrolyte brush on the surface of casein micelles, Colloids Surfaces A, 1996, vol. 117, pp. 151-159.

7. Tuinier, R. and De Kruif, C.G., Stability of casein micelles in milk, Journal of Chemical Physics, 2002, vol. 117, pp. 1290-1295.

8. De Kruif, C.G., Supra-aggregates of casein micelles as a prelude to coagulation, Journal of Dairy Science, 1998, vol. 81, pp. 3019--3028.

9. Udabage, P., McKinnon, I.R., and Augustin, M.A., Effects of mineral salts and calcium chelating agents on the gelation of renneted skim milk, Journal of Dairy Science, 2001, vol. 84, pp. 1569-1575.

10. Tsioulpas, A., Michael, J.L., and Grandison, A.S., Effect of Minerals on Casein Micelle Stability of Cows’ Milk,, Journal of Dairy Research, 2007, vol. 74, pp. 167-173.

11. Osintsev, A.M., Bakhtin, N.A., Braginsky, V.I., and Ivanenko, O.V., Termograficheskiy metod issledovaniya koagulyatsii moloka (Thermographic method of investigation of milk coagulation), Syrodelie i maslodelie (Cheese making and butter making), 2005, no. 5, pp. 20--21.

12. Hori, T., Objective measurements of the process of curd formation during rennet treatment of milks by the hot wire method, Journal of Food Science, 1985, vol. 50, pp. 911--917.

13. Osintsev, A.M., Braginsky, V.I., Lapshakova, O.Yu., and Chebotarev, A.L., Rol´ ionov kaltsiya v kolloidnoi stabil´nosti mitsell kazeina (The role of calcium ions in the colloid stability of casein micelles), Tekhnika i tekhnologiya pishchevykh proizvodstv (Technique and technology of food production), 2009, no. 1, pp. 63--67.

14. Dalgleish, D.G. and Parker, T.G., Binding of calcium ions to bovine αs1-casein and precipitability of the protein-calcium ion complexes, Journal of Dairy Research, 1980, vol. 47, pp. 113--122.

15. Parker, T.G. and Dalgleish, D.G., Binding of calcium ions to bovine β-casein, Journal of Dairy Research, 1981, vol. 48, pp. 71--76.

16. Wahlgren, N.M., Dejmek, P., and Drakenberg, T., Binding of Mg2+ and Ca2+ to -casein A1: a multi-nuclear magnetic resonance study, Journal of Dairy Research, 1993, vol. 60, pp. 65--78.

17. Grimley, H.J., Grandison, A.S., and Lewis, M.J., The effect of calcium removal from milk on casein micelle stability and structure, Milchwissenschaft, 2010, vol. 65, pp. 151--154.

18. Philippe, M., Gaucheron, F., Le Graet, Y., Michel, F., and Garem, A., Physicochemical characterization of calcium-supplemented skim milk, Lait, 2003, vol. 83, pp. 45--59.

19. Vasbinder, A.J., Rollema, H.S., and De Kruif, C.G., Impaired rennetability of heated milk; study of enzymatic hydrolysis and gelation kinetics, Journal of Dairy Science, 2003, vol. 86, pp. 1548--1555.

20. Sandra, S., Ho, M., Alexander, M., and Corredig, M., Effect of soluble calcium on the renneting properties of casein micelles as measured by rheology and diffusing wave spectroscopy, Journal of Dairy Science, 2012, vol. 95, pp. 75--82.

21. McSweeney, P.L., Olson, N.F., Fox, P.F., Healy, A., and Hojrup, P., Proteolytic specificity of chymosin on bovine alpha s1-casein, Journal of Dairy Research, 1993, vol. 60, pp. 401--412.

22. McSweeney, P.L.H., Fox, P.F., and Olson, N.F., Proteolysis of bovine caseins by cathepsin D: Preliminary observations and comparison with chymosin, International Dairy Journal, 1995, vol. 5, pp. 321--336.

23. Hynes, E.R., Aparo, L., and Candioti, M.C., Influence of residual milk-clotting enzyme on s1 casein hydrolysis during ripening of Reggianito Argentino cheese, Journal of Dairy Science, 2004, vol. 87, pp. 565--573.

24. Holt, C. and Horne, D.S., The hairy casein micelle: Evolution of the concept and its implications for dairy technology, Netherlands Milk and Dairy Journal, 1996, vol. 50, pp. 85--111.

25. McMahon, D.J. and McManus, W.R., Rethinking casein micelle structure using electron microscopy, Journal of Dairy Science, 1998, vol. 81, pp. 2985--2993.

26. Dalgleish, D.G., Spagnuolo, P.A., and Goff, H.D., A possible structure of the casein micelle based on high-resolution field-emission scanning electron microscopy, International Dairy Journal, 2004, vol. 14, pp. 1025--1031.

27. Lencki, R.W., Evidence for fibril-like structure in bovine casein micelles, Journal of Dairy Science, 2007, vol. 90, pp. 75--89.

28. Choi, J., Horne, D.S. and Lucey, J.A., Effect of insoluble calcium concentration on rennet coagulation properties of milk, Journal of Dairy Science, 2007, vol. 90, pp. 2612--2623.

29. O´Sullivan, M.M.. Kelly, A.L., and Fox, P.F., Influence of transglutaminase treatment on some physico-chemical properties of milk, Journal of Dairy Research, 2002, vol. 69, pp. 433--442.

30. Vasbinder, A.J., Rollema, H.S., Bot, A., and De Kruif, C.G., Gelation mechanism of milk as influenced by temperature and pH; studied by the use of transglutaminase cross-linked casein micelles, Journal of Dairy Science, 2000, vol. 86, pp. 1556--1563.

31. Canabady-Rochelle, L.S., Sanchez, C., Mellema, M., Bot, A., Desobry, S., and Banon, S., Influence of calcium salt supplementation on calcium equilibrium in skim milk during pH cycle, Journal of Dairy Science, 2007, vol. 90, pp. 2155-2162.


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