Demineralization of Crab Shells by Chemical and Biological Treatments

  • Jung Woo-Jin (Glucosamine Saccharide Materials-National Research Laboratory (GSM-NRL), Division of Applied Bioscience and Biotechnology, Institute of Agricultural Science and Technology, Chonnam National University) ;
  • Jo Gyung-Hyun (Glucosamine Saccharide Materials-National Research Laboratory (GSM-NRL), Division of Applied Bioscience and Biotechnology, Institute of Agricultural Science and Technology, Chonnam National University) ;
  • Kuk Ju-Hee (Glucosamine Saccharide Materials-National Research Laboratory (GSM-NRL), Division of Applied Bioscience and Biotechnology, Institute of Agricultural Science and Technology, Chonnam National University) ;
  • Kim Kil-Yong (Glucosamine Saccharide Materials-National Research Laboratory (GSM-NRL), Division of Applied Bioscience and Biotechnology, Institute of Agricultural Science and Technology, Chonnam National University) ;
  • Park Ro-Dong (Glucosamine Saccharide Materials-National Research Laboratory (GSM-NRL), Division of Applied Bioscience and Biotechnology, Institute of Agricultural Science and Technology, Chonnam National University)
  • Published : 2005.02.01

Abstract

To achieve demineralization of crab shell waste by chemical and biological treatments, lactic acid and lactic acid bacterium were applied. In 5.0 and $10\%$ lactic acid, pH rapidly decreased from 6.8 to 4.2 and from 4.5 to 2.4 at day 3, respectively, and thereafter the pH remained at an almost constant level. In a $10\%$ lactic acid bacterium inoculum, pH lowered to 4.6 at day 5. Relative residual ash content rapidly decreased to 49.1 and $16.4\%$ in 5 and $10\%$ lactic acid treatments, respectively, for the initial 12 h. In 2.5, 5 and $10\%$ lactic acid bacterium inoculums, relative residual ash content rapidly decreased to 55.2, 40.9 and $44.7\%$, respectively, on the first day. Residual dry masses were 76.4, 67.8 and $46.6\%$ in 2.5, 5 and $10\%$ lactic acid treatments, respectively, for the initial 12 h. After a one-time exchange of the lactic acid solution, in the $5.0\%$ lactic acid treatment, residual dry mass rapidly decreased from 66.0 to $41.4\%$. In 2.5, 5 and $10\%$ lactic acid bacterium inoculums, residual dry masses decreased to 67.6, 57.4 and $59.6\%$ respectively, on the first day. Protein contents after demineralization ranged from $51.3{\sim}54.7\%$ in the chemical treatments and decreased to $32.3\%$ in the lactic acid fermentation process. A negative relationship was shown between pH and demineralization rate in lactic acid and lactic acid bacterium treatments. These results suggest that lactic acid fermentation can be an alternative for demineralization of crab shells, even though the rate and efficiency of the demineralization is lower than the chemical treatment.

Keywords

References

  1. Hackman, R. H. (1954) Chitin. 1. Enzyme degradation of chitin and chitin esters. Austr. J. Biol. Sci. 7: 168-178 https://doi.org/10.1071/BI9540168
  2. Whistler, R. S. and J. N. BeMiller (1962) Chitin. J. Org. Chem. 27: 1161-1163 https://doi.org/10.1021/jo01051a009
  3. Allan, G. G., J. R. Fox, and N. Kong (1978) Marine polymers. Part 8. A critical evaluation of the potential sources of chitin and chitosan. pp. 64-78. In: R. A. A. Muzzarelli and E. R. Pariser (eds.). Proceeding of 1st International Conference on Chitin/Chitosan. MIT Sea Grant Rep. MITSG, USA
  4. Ng, C. H., S. Chandrkrachang, and W. F. Stevens (2000) Effect of the rate of deacetylation on the physico-chemical properties of cuttlefish chitin. Adv. Chitin Science 4: 50-54
  5. Myint, K. T., C. H. Ng, S. Chandrkrachang, and W. F. Stevens (2002) Optimal demineralization of crab shells wastes for chitin production. pp. 15-18. In: K. Scchiva, S. Chandrkrachang, P. Methacanon, and M. G. Peter (eds.). Advance in Chitin Science. Vol. V. Proceeding of the 5th Asia Pacific Chitin and Chitosan Symposium & Exhibition. Bangkok, Thailand
  6. Stevens, W. F. (2002) Production and storage of high quality chitosan from shrimp, crab and fungus. pp. 6-11. In: K. Scchiva, S. Chandrkrachang, P. Methacanon, and M. G. Peter (eds.). Advance in Chitin Science. Vol. V. Proceeding of the 5th Asia Pacific Chitin and Chitosan Symposium & Exhibition. Bangkok, Thailand
  7. A.O.A.C. (1980) Official Methods of Analysis of the Association of Official Analytical Chemists. Washington DC., USA
  8. Takiguchi, Y, K. Ohkouchi, H. Yamashita, and K. Shimahara (1987) A new method for quantitative determination of protein associated with crustacean chitin. Nippon Nogei Kagaku Kaishi. 61: 437-441 https://doi.org/10.1271/nogeikagaku1924.61.437
  9. Roberts, G. A. (1998) Chitosan production routes and their role in determining the structure and properties of the products. pp. 22-31. In: A, Domard, G. A. F. Roberts, and K. M. Varum (eds.). Advances in Chitin Science. Vol. II. Jacques Andres, Lyon, France
  10. Peniston, Q. P. and E. L. Johnson (1978) Demineralization of crustacea shells. US Patent 4,066,735
  11. Horowitz, S. T., S. Roseman, and H. J. Blumenthal (1957) Preparation of glucosamine oligoshaccharides: 1. Separation. J. Am. Chem. Soc. 79: 5046-5049 https://doi.org/10.1021/ja01575a059
  12. Bautisa, J., O. Cremades, R. Corpas, R. Ramos, F. Iglesias, J. Vega et al. (2000) Preparation of chitin by acetic acid fermenation. pp. 28-33. In: M. G. Peter, A. Domard, and A. A. Muzzaralli (eds.). Advences in Chitin Science. Vol. 4. University of Potsdam, Potsdam, Germany
  13. Zakaria, Z., G. M. Hall, and G. Shama (1998) Lactic acid fermentation of scampi waste in a rotating horizontal bioreactor for chitin recovery. Process Biochem. 33: 1-6 https://doi.org/10.1016/S0032-9592(97)00069-1
  14. Takeda, M. and E. Abe (1962) Isolation of crustacean chitin: Decalcification by disodium ethylenediaminotetraacetate and enzymic hydrosis of incidental proteins. Norisho Suisan Koshusho Kenkyu Hokoku 11: 339-406
  15. Takeda, M. and H. Katsuura (1964) Purification of king crab chitin. Suisan Daigaku Kenkyu Hokoku 13: 109-116
  16. Lin, J. Q., S. M. Lee, and Y. M. Koo (2004) Modeling and simulation of lactic acid fermentation with inhibition effects of lactic acid and glucose. Biotechnol. Bioprocess Eng. 9: 52-58 https://doi.org/10.1007/BF02949322
  17. Lin, J. Q., S. M. Lee, and Y. M. Koo (2004) Modeling and simulation of lactic acid fermentation with inhibition effects of lactic acid and glucose. Biotechnol. Bioprocess Eng. 9: 52-58 https://doi.org/10.1007/BF02949322
  18. Cira, L. A., S. Huerta, G. M. Hall, and K. Shirai (2002) Piot scale lactic acid fermentation of shrimp wastes for chitin recovery. Process Biochem. 37: 1359-1366 https://doi.org/10.1016/S0032-9592(02)00008-0
  19. Shirai, K, I. Guerrero, S. Huerta, G Saucedo, A. Castillo, R. O. Gonzalez, and G. M. Hall (2001) Effect of initial glucose concentration and inoculation level of lactic acid bacteria in shrimp waste ensilation. Enzym. Microbial. Technol. 28: 446-452 https://doi.org/10.1016/S0141-0229(00)00338-0
  20. Hall, G. M. and S. Silva (1991) Lactic acid fermentation of shrimp (Penaus monodon) waste for chitin recovery. pp. 633-638. In: C. J. Brine, P. A. Sandford, and J. P. Zikakis (eds.). Advance Chitin and Chitosan. 5th International Conference on Chitin & Chitosan. Elsevier, London, UK