K-Casein

K-Casein (or Kappa-casein, k casein, kappa casein) is a mammalian milk protein involved in a number of important physiological processes. In the gut, the ingested protein is split into an insoluble peptide (para kappa-casein) and a soluble hydrophilic glycopeptide (caseinomacropeptide). Caseinomacropeptide is responsible for increased efficiency of digestion, prevention of neonate hypersensitivity to ingested proteins, and inhibition of gastric pathogens.[1]

Contents

Structure

Scheme of a micelle.
Molecular surface model of K-Casein (Mod. of Kumosinski et al.,1993).

Caseins are a family of phosphoproteins (αS1, αS2, β, κ) that account for nearly 80% of bovine milk proteins (Lucey et al., 2003) and that form soluble aggregates because of the κ-casein molecules that stabilize the micellar structure. There are several models that account for the special conformation of casein in the micelles (Dalgleish, 1998). One of them proposes that the micellar nucleus is formed by several submicelles, the periphery consisting of microvellosities of κ-casein (Walstra, 1979; Lucey, 2002). Another model suggests that the nucleus is formed by casein-interlinked fibrils (Holt, 1992). Finally, the most recent model (Horne, 1998) proposes a double link among the caseins for gelling to take place. All 3 models consider micelles as colloidal particles formed by casein aggregates wrapped up in soluble κ-casein molecules. Milk-clotting proteases act on the soluble portion, κ-casein, thus originating an unstable micellar state that results in clot formation (Vasbinder et al.., 2003).

Milk Clotting

In red/blue Phe105-Met106 bond of κ- casein (Mod. of Kumosinski et al.,1993.)

Chymosin (EC 3.4.23.4) is an aspartic protease that specifically hydrolyzes the peptide bond in Phe105-Met106 of κ- casein and is considered to be the most efficient protease for the cheesemaking industry (Rao et al.., 1998). However, there are milk-clotting proteases able to cleave other peptide bonds in the κ-casein chain, such as the endothiapepsin produced by Endothia parasitica (Drohse et al.., 1989). There are also several milk-clotting proteases that, being able to cleave the Phe105-Met106 bond in the κ-casein molecule, also cleave other peptide bonds in other caseins, such as those produced by Cynara cardunculus (Lucey, 2002; Esteves et al.., 2003; Silva and Malcata, 2005) or even bovine chymosin (Kobayashi, 2004). This allows the manufacture of different cheeses with a variety of rheological and organoleptic properties.

The milk-clotting process consists of 3 main phases (Carlson et al.., 1987a):

  1. Enzymatic degradation of κ-casein
  2. Micellar flocculation
  3. Gel formation

Each step follows a different kinetic pattern, the limiting step in milk-clotting being the degradation rate

of κ-casein. The kinetic pattern of the second step of the milk-clotting process is influenced by the cooperative nature of micellar flocculation (Carlson et al.., 1987b; Silva and Malcata, 2005) whereas the rheological properties of the gel formed depend on the type of action of the proteases, the type of milk, and the patterns of casein proteolysis (Silva and Malcata, 2005). The overall process is influenced by several different factors, such as pH or temperature (Esteves et al.., 2003; Vasbinder et al.., 2003).

Michaelis-Menten saturation curve.

The conventional way of quantifying a given milkclotting enzyme (Poza et al.., 2003) employs milk as the substrate and determines the time elapsed before the appearance of milk clots. However, milk clotting may take place without the participation of enzymes because of variations in physicochemical factors, such as low pH or high temperature (Lucey, 2002; Lucey et al.., 2003; Vasbinder et al.., 2003). Consequently, this may lead to confusing and irreproducible results, particularly when the enzymes have low activity. At the same time, the classical method is not specific enough, in terms of setting the precise onset of milk gelation, such that the determination of the enzymatic units involved becomes difficult and unclear. Furthermore, although it has been reported that κ-casein hydrolysis follows typical Michaelis-Menten kinetics (Carlson et al.., 1987a), it is difficult to determine with the classic milk-clotting assay. To overcome this, several alternative methods have been proposed, such as the determination of halo diameter in agar-gelified milk (Poza et al.., 2003), colorimetric measurement (Hull, 1947), or determination of the rate of degradation of casein previously labeled with either a radioactive tracer (Christen, 1987) or a fluorochrome compound (Twining, 1984). All these methods use casein as the substrate to quantify proteolytic or milkclotting activities.

FTC-K-Casein Assay

Fluorescein isothiocyanate

K-casein labeled with the fluorochrome fluorescein isothiocyanate (FITC) to yield the fluorescein thiocarbamoyl (FTC) derivative. This substrate is used to deternimate the milk clotting activity of proteases (Ageitos, et al., 2006).

FTC-κ-casein method affords accurate and precise determinations of κ-caseinolytic degradation, the first step in the milk-clotting process. This method is the result of a modification to the one described by S.S. Twining (1984). The main modification was substituting the substrate previously used (casein) by -casein labeled with the fluorochrome fluorescein isothiocyanate (FITC) to yield the fluorescein thiocarbamoyl (FTC) derivative. This variation allows quantification of the -casein molecules degraded in a more precise and specific way, detecting only those enzymes able to degrade such molecules. The method described by Twining (1984), however, was designed to detect the proteolytic activity of a considerably large variety of enzymes. FTC-κ-casein allows the detection of different types of proteases at levels when no milk clotting is yet apparent, unveiling its higher sensitivity over currently used assay procedures. Therefore, the method may find application as an indicator during the purification or characterization of new milk-clotting enzymes.

References

  • Ageitos, J.M., Vallejo, J.A., Poza, M. and Villa, T.G. (2006) Fluorescein thiocarbamoyl-kappa-casein assay for the specific testing of milk-clotting proteases. J Dairy Sci 89, 3770–3777.[2]
  • Carlson, A., C. G. Hill, Jr., and N. F. Olson. 1987a. Kinetics of milk coagulation: I. The kinetics of kappa casein hydrolysis in the presence of enzyme deactivation. Biotechnol. Bioeng. 29:582–589.
  • Carlson, A., C. G. Hill, Jr., and N. F. Olson. 1987b. Kinetics of milk coagulation: II. Kinetics of the Secondary Phase. Micelle Flocculation. Biotechnol. Bioeng. 29:590–600.
  • Christen, G. L. 1987. A rapid method for measuring protease activity in milk using radiolabeled casein. J. Dairy Sci. 70:1807–1814.[3]
  • Dalgleish, D. G. 1998. Casein micelles as colloids. Surface structures and stabilities. J. Dairy Sci. 81:3013–3018.
  • Drohse, H. B., B. Foltmann, and B. Foltmann. 1989. Specificity of milk-clotting enzymes towards bovine kappa-casein. Biochim. Biophys. Acta. 995:221–224.
  • Esteves, C. L. C., J. A. Lucey, T. Wang, and E. M. V. Pires. 2003. Effect of pH on the gelation properties of skim milk gels made from plant coagulants and chymosin. J. Dairy Sci. 86:2558–2567.[4]
  • Holt, C. 1992. Structure and stability of bovine casein micelles. Adv. Protein Chem. 43:63–151.
  • Horne, D. S. 1998. Casein interactions: Casting light on the black boxes, the structure in dairy products. Int. Dairy J. 8:171–177.
  • Hull, M. E. 1947. Studies on milk proteins. II. Colorimetric determination of the partial hydrolysis of proteins in milk. J. Dairy Sci. 30:881–884.
  • Kobayashi, H. 2004. Polyporopepsin. Pages 113–115 in Handbook of Proteolytic Enzymes. 2nd ed. A. J. Barrett, N. D. Rawlings, and J. F. Woessner, ed. Elsevier, London, UK.
  • Kumosinski T. F., E. M. Brown, and H. M. Farrell, Jr., Kappa-Casein variant B structure: Three-Dimensionsl Molecular Modeling of Bovine Caseins: A Refined, Energy-Minimized Kappa-Casein Structure (1993) Journal of Dairy Science, 76:2507-2520.
  • Lucey, J. A. 2002. ADSA Foundation Scholar Award Formation and Physical Properties of Milk Protein Gels. J. Dairy Sci. 85:281–294.[5]
  • Lucey, J. A., M. E. Johnson, and D. S. Horne. 2003. Invited review: Perspectives on the basis of the rheology and texture properties of cheese. J. Dairy Sci. 86:2725–2743.[6]
  • Poza, M., C. Sieiro, L. Carreira, J. Barros-Vela´zquez, and T. G. Villa. 2003. Production and characterization of the milk-clotting protease of Myxococcus xanthus strain 422. J. Ind. Microbiol. Biotechnol. 30:691–698.[7]
  • Rao, M. B., A. M. Tanksale, M. S. Ghatge, and V. V. Deshpande. 1998. Molecular and biotechnological aspects of microbial proteases. Microbiol. Mol. Biol. Rev. 62:597–635.[8]
  • Silva, S. V., and F. X. Malcata. 2005. Partial identification of watersoluble peptides released at early stages of proteolysis in sterilized ovine cheese-like systems: Influence of type of coagulant and starter. J. Dairy Sci. 88:1947–1954.[9]
  • Twining, S. S. 1984. Fluorescein isothiocyanate-labeled casein assay for proteolytic enzymes. Anal. Biochem. 143:30–34.[10]
  • Vasbinder, A. J., H. S. Rollema, A. Bot, and C. G. de Kruif. 2003. Gelation mechanism of milk as influenced by temperature and pH; Studied by the use of transglutaminase cross-linked casein micelles. J. Dairy Sci. 86:1556–1563.[11]
  • Walstra, P. 1979. The voluminosity of bovine casein micelles and some of its implications. J. Dairy Res. 46:317–322.

External links


Wikimedia Foundation. 2010.

Look at other dictionaries:

  • Casein — oder Kasein (lat. caseus = Käse) ist der Name für denjenigen Proteinanteil der Milch der höheren Säugetiere, der nicht in die Molke gelangt und der beispielsweise zu Käse weiterverarbeitet wird. Es ist eine Mischung aus mehreren Proteinen (αS1,… …   Deutsch Wikipedia

  • Casein paint — Casein paint, derived from milk, is a fast drying, water soluble medium used by artists. It generally has a glue like consistency, but can be thinned with water to the degree that fits a particular artist s style and desired result. It can be… …   Wikipedia

  • Casein kinase — can refer to: * Casein kinase 1 * Casein kinase 2 …   Wikipedia

  • Casein kinases — may refer to: * Casein kinase 1 * Casein kinase 2 …   Wikipedia

  • Casein nutrient agar — (CN) is a growth medium used to culture isolates of lactic acid bacteria such as Streptococcus thermophilus and Lactobacillus bulgaricus . It is composed of standard nutrient agar with the added ingredient of skim milk powder, which contains… …   Wikipedia

  • Casein Aralac — Aralac is a protein fibre produced by precipitating casein from skim milk, dissolving it in an alkaline solution, ageing, spinning by extrusion through spinnerets into an acid bath, cutting the continuous filaments into the desired staple lengths …   Dictionary of the English textile terms

  • Casein — Ca se*in, n. [Cf. F. cas[ e]ine, fr. L. caseur cheese. Cf. {Cheese}.] (Physiol. Chem.) A proteid substance present in both the animal and the vegetable kingdom. In the animal kingdom it is chiefly found in milk, and constitutes the main part of… …   The Collaborative International Dictionary of English

  • Caseïn — (Käsestoff), stickstoffhaltige Substanz des Thier u. Pflanzen reichs, Zusammensetzung nach Mulder: 10(C40H31N10O12) + S; findet sich in der Milch aller Säugethiere, theils gelöst. theils ungelöst als Hüllenmembran der Milchkügelchen; ferner kommt …   Pierer's Universal-Lexikon

  • Caseïn — Caseïn, Käsestoff, gehört zu den sog. Proteïnstoffen und findet sich hauptsächlich in der Milch der Säugethiere, in deren Zusammensetzung er einen Hauptbestandtheil bildet. Aus ihr stellt man ihn gewöhnlich durch Zusatz von Säuren oder Lab dar,… …   Herders Conversations-Lexikon

  • casein kinase II phosphorylation site — Casein kinase II phosphorylates exposed Ser or sometimes Thr residues, provided that an acidic residue is present three residues from the phosphate acceptor site. Consensus pattern: (S/T) x x (D/E) …   Dictionary of molecular biology

  • Casein — vgl. Kasein …   Das Wörterbuch medizinischer Fachausdrücke

Share the article and excerpts

Direct link
Do a right-click on the link above
and select “Copy Link”

We are using cookies for the best presentation of our site. Continuing to use this site, you agree with this.