Synthesis, organotin(IV) benzoate, anticancer
Pavel Mokrejs1, Dagmar Janacova2, Karel Kolomaznik2, Vladimir Vase
¹Tomas Bata University, Faculty of Technology, Department of Polymeric Engineering, Nam. TGM 275, 762 72 Zlin, (The Czech Republic). ²Tomas Bata University, Faculty of Applied Informatics, Department of Processing Control and Applied Computer Science, Nad Stranemi 4511, 760 05 Zlin (The Czech Republic).
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Article Accepted on :
Article Published : 03 Sep 2010
The presented work deals with possibilities in isolating amaranth protein. A biochemical procedure was chosen, consisting in employing enzymes acting specifically on protein degradation. Experiments were executed through two-level factor tests, and the influences under study were those of enzymatic hydrolysis duration (1 and 5 h) and temperature (30 and 50 o C) on efficiency of protein hydrolysis. Amaranth flour was mixed with water in ratio 1:20, heating to desired temperature proceeded at a rate of 2 o C.min-1, and 0.1 % enzyme (per mass of flour) was added. Centrifugation yielded a protein hydrolysate and a solid, polysaccharide-enriched fraction.
KEYWORDS:Amaranth; enzyme; isolation; protein; protein hydrolysate
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Copy the following to cite this article: Mokrejs P, Janacova D, Kolomaznik K, Vase V. Synthesis, organotin(IV) benzoate, anticancer. Orient J Chem 2010;26(3). |
Copy the following to cite this URL: Mokrejs P, Janacova D, Kolomaznik K, Vase V. Synthesis, organotin(IV) benzoate, anticancer. Available from: http://www.orientjchem.org/?p=11569 |
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