
SYNTHESIS AND ANALYSIS OF COPPER PROTEINATE AND MANGANESE PROTEINATE FROM REACTION OF COPPER SULFATE AND MANGANESE SULFATE WITH PROTEIN EXTRACTED FROM FISH WASTE
Author(s) -
Harmita Harmita,
Dannis Samuel Simbolon
Publication year - 2020
Publication title -
international journal of applied pharmaceutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.238
H-Index - 15
ISSN - 0975-7058
DOI - 10.22159/ijap.2020.v12s1.ff031
Subject(s) - manganese , chemistry , copper , bioavailability , hydrolysis , sulfate , metal , nuclear chemistry , biochemistry , organic chemistry , biology , bioinformatics
Objective: Copper and manganese are essential minerals needed for various biological processes in small amounts. However, essential mineralsare poorly absorbed in the form of salts or free form, leading to their low bioavailability. Forming complexes of essential minerals with protein canincrease their bioavailability. Metal proteinate complexes are non-polar, thereby reducing their excretion from the body. Fish waste is quite abundantin Indonesia, and therefore, we used fish waste to synthesize metal-proteinate complexes.Methods: Protein was extracted from fish waste using pancreatin. The extracted protein was mixed with copper or manganese in various ratios. Themetal content in the complexes was analyzed using atomic absorption spectrophotometry; ion exchange chromatography was used for separating thecomplexes from free unbound metals.Results: The optimum condition which yielded the highest protein content was the ratio of pancreatin enzyme to fish waste powder of 2:100. Theoptimum concentration of pancreatin was found to be 2% of the substrate. The yield of copper-proteinate complexes ranged from 97.87% to 98.55%,whereas the yield of manganese proteinate ranged from 97.05% to 98.36%. The free metal content was only found in the manganese proteinatecomplex in the 1.2:1 ratio, which was determined to be 0.0198 mg/g.Conclusion: We demonstrated that copper and manganese can react with proteins extracted by enzymatic hydrolysis of fish waste.