A three step approach for the purification of alkaline phosphatase from non-pasteurized milk

被引:0
作者
Lata Sheo Bachan Upadhyay
Nishant Verma
机构
[1] National Institute of Technology,Department of Biotechnology
来源
Journal of Food Science and Technology | 2015年 / 52卷
关键词
Alkaline Phosphatase; Purification; Enzyme; Milk; n-butanol;
D O I
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中图分类号
学科分类号
摘要
In this study, a three step purification of alkaline phosphatase from non-pasteurized milk has been described. It included cream extraction, n-butanol treatment and acetone precipitation. Different parameters such as buffer concentration, temperature, pH, substrate concentration, acetone and n-butanol treatment were optimized to maximize the enzyme activity. The enzyme was fruitfully purified up to homogeneity from the milk, with percentage recovery and fold purification of 56.17 and 17.67 respectively. The kinetic parameters were determined to be 0.927 mM (Km) and 55.86 μM/min (Vmax), with specific activity of 11.31 U/mg. Other optimized parameters were estimated as a buffer concentration of 0.5 M with pH 9.0, temperature optima at 37 °C, with n-butanol and acetone concentration of 20 % (v/v) and 50 % (v/v) respectively. This approach provides a simple and effective method for the purification of alkaline phosphatase from non-pasteurized milk.
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页码:3140 / 3146
页数:6
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  • [1] Ahn YS(1993)Selective extraction of alkaline phosphatase and 5′-nucleotidase from milk fat globule membranes by a single phase n-butanol procedure Prep Biochem 23 409-419
  • [2] Snow LD(2011)Evaluation of alkaline phosphatase detection in dairy products using a modified rapid chemiluminescent method and official methods J Food Prot 74 1144-1154
  • [3] Albillos SM(1987)Purification of extracellular alkaline phosphatase released by Escherichia coli excretory mutants Appl Microbiol Biotechnol 50 64-71
  • [4] Reddy R(2013)Kinetic behaviour of calf intestinal alkaline phosphatase with pNPP Indian J Biochem Biophys 30 401-407
  • [5] Salter R(2002)Kinetic studies with alkaline phosphatase in the presence and absence of inhibitors and divalent cations Biochem Mol Biol Educ 42 27-32
  • [6] Atlan D(2004)Thermal and carbon dioxide inactivation of alkaline phosphatase in buffer and milk Food Technol Biotechnol 2 33-38
  • [7] Portalier R(2002)Effects of tricine, glycine and tris buffers on alkaline phosphatase activity J Exp Microbiol Immunol 53 509-516
  • [8] Chaudhuri G(2008)Purification and biochemical characterization of thermostable alkaline phosphatases produced by Rhizopus microsporus var. rhizopodiformis Folia Microbiol (Praha) 40 688-704
  • [9] Chatterjee S(1994)Enzymes in diagnostics: achievements and possibilities of recombinant DNA technology Clin Chem 193 265-275
  • [10] Venu-Babu P(1951)Protein measurement with the Folin phenol reagent J Biol Chem 48 175-178