1. Trang chủ
  2. » Luận Văn - Báo Cáo

Extraction and characterization of fish protein isolate from yellowfin (thunnus albacares) dark muscle using ph shift method

92 7 0

Đang tải... (xem toàn văn)

Tài liệu hạn chế xem trước, để xem đầy đủ mời bạn chọn Tải xuống

THÔNG TIN TÀI LIỆU

Thông tin cơ bản

Định dạng
Số trang 92
Dung lượng 3,22 MB

Nội dung

MINISTRY OF EDUCATION AND TRAINING NHA TRANG UNIVERSITY LAURINE MULE MUENI 60CH300 EXTRACTION AND CHARACTERIZATION OF FISH PROTEIN ISOLATE FROM YELLOWFIN (Thunnus albacares) DARK MUSCLE USING pH-SHIFT METHOD MASTER THESIS KHANH HOA – 2020 MINISTRY OF EDUCATION AND TRAINING NHA TRANG UNIVERSITY LAURINE MULE MUENI 60CH300 EXTRACTION AND CHARACTERIZATION OF FISH PROTEIN ISOLATE FROM YELLOWFIN (Thunnus albacares) DARK MUSCLE USING pH-SHIFT METHOD MASTER THESIS FOOD TECHNOLOGY Major: Topic allocation Decision Decision on establishing the Committee: Defense date: Supervisors: Dr Nguyen Trong Bach (Principal supervisor) Dr Bui Tran Nu Thanh Viet (Co-Supervisor) Chairman: Faculty of Graduate Studies: KHANH HOA - 2020 UNDERTAKING I undertake that the thesis entitled: “Extraction and characterization of fish protein isolate from Yellowfin (Thunnus albacares) dark muscle using pH-shift method” is my own work The work has not been presented elsewhere for assessment until the time this thesis is submitted 26 September 2020 Laurine Mule Mueni iii FUNDING This research was funded by National Foundation for Science and Technology Development - Ministry of Science and Technology of Vietnam in the Nafosted project with No 106.99-2018.42 iv ACKNOWLEDGMENT First and foremost, I wish to thank God Almighty for His grace and strength and how He has been with me throughout my study period in Vietnam I would like to express the deepest appreciation to the Faculty of Food Technology, Nha Trang University in cooperation with the VLIR-UOS program for helping and giving me the best conditions to finish my thesis In addition, I would like to thank the National Foundation for Science and Technology Development - Ministry of Science and Technology of Vietnam in the Nafosted project with No 106.99-2018.42 for financial support to the research My special and deep appreciations go to my supervisors Dr Nguyen Trong Bach and Dr Bui Tran Nu Thanh Viet for their continuous support of my master‟s studies and research, for their patience, motivation, enthusiasm, and immense knowledge Their guidance helped me in all the time of research and writing of this thesis Last but not the least; I would like to thank my family: my guardian, my friends, classmates and colleagues for supporting me spiritually, mentally and physically throughout writing this thesis 26 September 2020, Nha Trang Laurine Mule Mueni v TABLE OF CONTENTS UNDERTAKING iii FUNDING iv ACKNOWLEDGMENT v TABLE OF CONTENTS .vi LIST OF ABBREVIATIONS ix LIST OF TABLES x LIST OF FIGURES xi ABSTRACT xiii GENERAL INTRODUCTION .1 PROBLEM STATEMENT CHAPTER : BACKGROUND 1.1 Tuna fish and its by-products 1.1.1 Tuna productions 1.1.2 The composition of yellowfin dark muscle 1.1.2.1 Myofibrillar proteins 1.1.2.2 Sarcoplasmic proteins 1.1.2.3 Lipids 1.1.3 Tuna by-product 10 1.2 Factors affecting the utilization of TDM 11 1.2.1 The dark colour and Myoglobin oxidation 11 1.2.2 Lipid and protein oxidation 13 1.2.3 Histamine 15 1.3 Protein extraction techniques used and FPI utilization 16 1.3.1 pH –shift method 17 vi 1.3.2 Protein recovery 19 1.3.3 By-products and FPI utilization 20 1.3.4 Fish protein isolate characterization .21 CHAPTER : MATERIALS AND METHODS 24 2.1 Materials collection and preparation .24 2.1.1 Dark muscle 24 2.1.2 Chemicals .24 2.1.3 FPI extraction by pH-shift method .24 2.2 Methods of characterization 26 2.2.1 Fourier transform infrared (FTIR) spectroscopic analysis 27 2.2.2 Zeta potential 28 2.2.3 Light scattering .29 2.2.4 Turbidity measurements .31 2.2.5 Determination of the protein concentration with UV-Visible spectroscopy 31 2.2.6 Confocal laser scanning microscopy 32 2.2.7 Sodium Dodecyl Sulfate Polyacrylamide Gel Electrophoresis (SDS- page) .33 2.2.8 Viscosity measurement 36 2.2.9 Data analysis 37 CHAPTER 3: RESULTS AND DISCUSSIONS 38 3.1 FPI extraction 38 3.2 Characterization of TDMPI .39 3.2.1 Amino acids 39 3.2.2 Fourier-Transform Infrared Spectroscopy 41 3.2.3 Size-Exclusion Chromatography Analysis of TDMPI 43 3.3 Structure and physical properties of TDMPI solution 44 vii 3.3.1 Protein solubility 44 3.3.2 Light scattering .46 3.3.3 Micro-structure .47 3.3.4 SDS-PAGE 50 3.3.5 Zeta Potential of TDMPI solution 51 3.3.6 Viscosity of TDMPI solution .54 CONCLUSION AND OUTLOOK .57 REFERENCES 59 APPENDICES I Appendix 1: Test report of Amino acid in TDM II Appendix 2: Test report of Amino acid in TDM III Appendix 3: Test report of Amino acid in TDMPI IV Appendix 4: Test report of Amino acid in TDMPI V Appendix 5: Determination of histamine in TDM VI Appendix 6: Determination of histamine in TDMPI VII Appendix 7: Effect of pH (using NaOH) VIII viii LIST OF ABBREVIATIONS AA : Amino acid APS : Ammonium persulfate Cp : Protein concentration DI : Deionised water DLS : Dynamic Light Scattering EAA : Essential amino acid FPI : Fish protein isolate HMW : High molecular weight LMW : Low molecular weight LOD : Limit of detection LS : Light scattering MHC : Myosin heavy chain MLC : Myosin light chain MW : Molar mass NEAA : Non-essential amino acid pI : Isoelectric point Rg : Radius of gyration Rh : Hydrodynamic radius RI : Refractive index RPM :Revolutions per minute SLS : Static Light Scattering TAA : Total amino acid TEMED : Tetramethylethylenediamine TDM : Tuna dark muscle TDMPI : Tuna dark muscle protein isolate TWM : Tuna white muscle UV : Ultraviolet absorbance ix LIST OF TABLES Table 1.1: Proximate composition of the muscle tissue of yellowfin tuna (%, wet basis) .9 Table 1.2: Protein recovery yield from processing trout by-products by the isoelectric solubilisation/precipitation technology 20 Table 2.1: Recipe for stocking gel and resolving gel 35 Table 3.1: Proximate composition of TDM and TDMPI 39 Table 3.2: Amino acid composition of TDMPI powder, and reference proteins (dry basis) .40 Table 3.3: Effect of salt on pI of TDMPI in different ionic strengths 53 x 0014-Z Lee, H J., Park, S H., Yoon, I S., Lee, G W., Kim, Y J., Kim, J S., & Heu, M S (2016b) Chemical composition of protein concentrate prepared from Yellowfin tuna Thunnus albacares roe by cook-dried process Fisheries and Aquatic Sciences, 19(1), 1–8 https://doi.org/10.1186/S41240-016-0012-1 Love, R M (1970) H caspers I, 1970 Lund, M N., Heinonen, M., Baron, C P., & Estévez, M (2011) Protein oxidation in muscle foods: A review Molecular Nutrition and Food Research, 55(1), 83–95 https://doi.org/10.1002/mnfr.201000453 Marmon, S K., & Undeland, I (2010) Protein isolation from gutted herring (Clupea harengus) using pH-shift processes Journal of Agricultural and Food Chemistry, 58(19), 10480–10486 https://doi.org/10.1021/jf101057q Matak, K E., Tahergorabi, R., & Jaczynski, J (2015) A review: Protein isolates recovered by isoelectric solubilization/precipitation processing from muscle food by-products as a component of nutraceutical foods Food Research International, 77, 697–703 https://doi.org/10.1016/j.foodres.2015.05.048 McClements, D (2004) Food Emulsions in Practice Food Emulsions, 547–576 https://doi.org/10.1201/b18868-13 Muranyi, I S., Volke, D., Hoffmann, R., Eisner, P., Herfellner, T., Brunnbauer, M., Koehler, P., & Schweiggert-Weisz, U (2016) Protein distribution in lupin protein isolates from Lupinus angustifolius L prepared by various isolation techniques Food Chemistry, 207, 6–15 https://doi.org/10.1016/j.foodchem.2016.03.073 Muyonga, J H., Cole, C G B., & Duodu, K G (2004) Fourier transform infrared (FTIR) spectroscopic study of acid soluble collagen and gelatin from skins and bones of young and adult Nile perch (Lates niloticus) Food Chemistry, 86(3), 325–332 https://doi.org/10.1016/j.foodchem.2003.09.038 Nakamura, Y N., Ando, M., Seoka, M., Kawasaki, K ichi, & Tsukamasa, Y (2007) Changes of proximate and fatty acid compositions of the dorsal and ventral ordinary muscles of the full-cycle cultured Pacific bluefin tuna Thunnus orientalis with the growth Food Chemistry, 65 103(1), 234–241 https://doi.org/10.1016/j.foodchem.2006.07.064 Nano, T Z., Lei, Z., Chen, X D., Mercadé-Prieto, R., Gbassi, G., Yolou, F., Sarr, S., Atheba, P., Amin, C., Ake, M., Dukhin, A S., Parlia, S., Kaszuba, M., Corbett, J., Watson, F M N., Jones, A., Cheung, L., Wanasundara, J., Nickerson, M T., Jandt, K D (2018) High-concentration zeta potential measurements using lightscattering techniques Food Hydrocolloids, 368(1), 1–15 https://doi.org/10.1016/j.colsurfb.2014.02.048 Neves, A C (2015) Extraction, purification and charecterization of biofunctional peptides from marine processinf co-products Ireland Nguyen, H T M., Tran, L T., Sylla, K S B., Randriamahatody, Z., Donnay-Moreno, C., Bergé, J P., & Moreau, J (2011) Enzymatic hydrolysis of yellowfin tuna (Thunnus albacares) by-products using protamex protease Food Technology and Biotechnology, 49(1), 48–55 http://www.ftb.com.hr/49/FTB_49_48.html Nishioka, M., Tanioka, Y., Miyamoto, E., Enomoto, T., & Watanabe, F (2007) TLC analysis of a corrinoid compound from dark muscle of the yellowfin tuna (Thunnus albacares) Journal of Liquid Chromatography and Related Technologies, 30(15), 2245–2252 https://doi.org/10.1080/10826070701451605 Núñez-Flores, , Cando, D., Borderías, A J., & Moreno, H M (2018) Importance of salt and temperature in myosin polymerization during surimi gelation Food Chemistry, 239(January 2018), 1226–1234 https://doi.org/10.1016/j.foodchem.2017.07.028 P Elizondo-Garza, S.O Serna-Sald´ıvar, C C.-H ´ * (2016) Protein recovery from skipjack tuna (Katsuwonus pelamis) wash water with different pH and temperature combinations Lc Gc, 13(2), 132–142 Panggat, E B (2003) Product Innovations from tuna and milkfish processing byproducts for human food consumption: Generalization of By-products from tuna and milkfish processing Tuna By-products Park, J D., Poowakanjana, S., & Park, J W (2012) Biochemical properties of pelagic fish proteins as affected by isolation methods and gel properties by heating methods Journal of Aquatic Food Product Technology, 21(4), 307–320 66 https://doi.org/10.1080/10498850.2011.594977 Park, J., Kristinsson, H., Lanier, T., Halldorsdottir, S., Geirsdottir, M., & Park, J (2013) Fish Protein Isolate by pH Shift Surimi and Surimi Seafood, Third Edition, 169–192 https://doi.org/10.1201/b16009-8 Park, J., Lanier, T., Yongsawatdigul, J., & Carvajal-Rondanelli, P (2013) Surimi Gelation Chemistry Surimi and Surimi Seafood, Third Edition, 101–140 https://doi.org/10.1201/b16009-6 Pazos, M., Medina, I., & Hultin, H O (2005) Effect of pH on hemoglobin-catalyzed lipid oxidation in cod muscle membranes in vitro and in situ Journal of Agricultural and Food Chemistry, 53(9), 3605–3612 https://doi.org/10.1021/jf0403890 Pegg, R B., & Shahidi, F (1997) Unraveling the Chemical Identity of Meat Pigments Critical Reviews in Food Science and Nutrition, 37(6), 561–589 https://doi.org/10.1080/10408399709527789 Peng, S., Chen, C., Shi, Z., & Wang, L (2013) Amino Acid and Fatty Acid Composition of the Muscle Tissue of Yellowfin Tuna (Thunnus Albacares) and Bigeye Tuna (Thunnus Obesus) Journal of Food and Nutrition Research, 1(4), 42–45 https://doi.org/10.12691/jfnr-1-4-2 Phan-xuan, T (2016) Elaboration of microgel protein particles by controlled selfassembling of heat-denatured beta-lactoglobulin To cite this version  :May Phan-Xuan, T., Thuresson, A., Skepö, M., Labrador, A., Bordes, , & Matic, A (2016) Aggregation behavior of aqueous cellulose nanocrystals: the effect of inorganic salts Cellulose, 23(6), 3653–3663 https://doi.org/10.1007/s10570-0161080-1 Qian, Z J., Je, J Y., & Kim, S K (2007) Antihypertensive effect of angiotensin I converting enzyme-inhibitory peptide from hydrolysates of bigeye tuna dark muscle, Thunnus obesus Journal of Agricultural and Food Chemistry, 55(21), 8398–8403 https://doi.org/10.1021/jf0710635 R Pecora (2000) Dynamic Light Scattering Measurement of Nanometer Particles in Liquids Journal of Nanoparticle Research, 2, 123–131 67 Richards, M P., Dettmann, M A., & Grunwald, E W (2005) Pro-oxidative characteristics of trout hemoglobin and myoglobin: A role for released heme in oxidation of lipids Journal of Agricultural and Food Chemistry, 53(26), 10231– 10238 https://doi.org/10.1021/jf051923m Richards, M P., & Hultin, H O (2002a) Contributions of blood and blood components to lipid oxidation in fish muscle Journal of Agricultural and Food Chemistry, 50(3), 555–564 https://doi.org/10.1021/jf010562h Richards, M P., Modra, A M., & Li, R (2002b) Role of deoxyhemoglobin in lipid oxidation of washed cod muscle mediated by trout, poultry and beef hemoglobins Meat Science, 62(2), 157–163 https://doi.org/10.1016/S0309-1740(01)00242-X Salgin, S., Salgin, U., & Bahadir, S (2012) Zeta potentials and isoelectric points of biomolecules: The effects of ion types and ionic strengths International Journal of Electrochemical Science, 7(12), 12404–12414 Sánchez-Zapata, E., Amensour, M., Oliver, R., Fuentes-Zaragoza, E., Navarro, C., Fernández-López, J., Sendra, E., Sayas, E., & Pérez-Alvarez, J A (2011) Quality Characteristics of Dark Muscle from Yellowfin Tuna Thunnus albacares to Its Potential Application in the Food Industry Food and Nutrition Sciences, 02(01), 22–30 https://doi.org/10.4236/fns.2011.21003 sản, T t (2017, 20) Retrieved from https://tongcucthuysan.gov.vn/tint%E1%BB%A9c/-ngh%E1%BB%81-c%C3%A1-th%E1%BA%BFgi%E1%BB%9Bi/doc-tin/006657/2016-12-26/tong-quan-thi-truong-ca-ngu-thegioi-11-thang-dau-nam-2016 Shaviklo, A R., Rezapanah, S., Motamedzadegan, A., Damavandi-Kamali, N., & Mozafari, H (2017) Optimum conditions for protein extraction from tuna processing by-products using isoelectric solubilization and precipitation processes Iranian Journal of Fisheries Sciences, 16(2), 774–792 Shaviklo, G R (2008) Evaluation and Utilisation of Fish Protein Isolate Products Evaluation and Utilisation of Fish Protein Isolate Products October, 1–95 Shaviklo, G R., Thorkelsson, G., & Arason, S (2010) Katki Maddeleri ve Donrurarak Saklamanin Mezgitten (Melanogrammus aeglefinus) Izole 68 Edilen Balik Proteininin Fonksiyonel Özellikleri ve Akis Davranisi Üzerine Etkisi Turkish Journal of Fisheries and Aquatic Sciences, 10(3), 333–340 https://doi.org/10.4194/trjfas.2010.0305 Sikorski, Z E (1994) The Myofibrillar Proteins in Seafoods Seafood Proteins, 40– 57 https://doi.org/10.1007/978-1-4615-7828-4_4 Singh, P., Benjakul, S., Maqsood, S., & Kishimura, H (2011) Isolation and characterisation of collagen extracted from the skin of striped catfish (Pangasianodon hypophthalmus) Food Chemistry, 124(1), 97–105 https://doi.org/10.1016/j.foodchem.2010.05.111 Sriprablom, J., Luangpituksa, P., Wongkongkatep, J., Pongtharangkul, T., & Suphantharika, M (2019) Influence of pH and ionic strength on the physical and rheological properties and stability of whey protein stabilized o/w emulsions containing xanthan gum Journal of Food Engineering, 242, 141–152 https://doi.org/10.1016/j.jfoodeng.2018.08.031 Stefansson, G., & Hultin, H O (1994) On the Solubility of Cod Muscle Proteins in Water Journal of Agricultural and Food Chemistry, 42(12), 2656–2664 https://doi.org/10.1021/jf00048a002 Surasani, V K R (2018) Acid and alkaline solubilization (pH shift) process: a better approach for the utilization of fish processing waste and by-products Environmental Science and Pollution Research, 25(19), 18345–18363 https://doi.org/10.1007/s11356-018-2319-1 Surasani, V K R., Tyagi, A., & Kudre, T (2017) Recovery of Proteins from Rohu Processing Waste Using pH Shift Method: Characterization of Isolates Journal of Aquatic Food Product Technology, 26(3), 356–365 https://doi.org/10.1080/10498850.2016.1186130 Swatland, H J (2012) Muscle iridescence in yellowfin tuna (Thunnus albacares) Food Research International, 48(2), 449–453 https://doi.org/10.1016/j.foodres.2012.05.018 Tahergorabi, R., Beamer, S K., Matak, K E., & Jaczynski, J (2012) Isoelectric solubilization/precipitation as a means to recover protein isolate from striped bass 69 (Morone saxatilis) and its physicochemical properties in a nutraceutical seafood product Journal of Agricultural and Food Chemistry, 60(23), 5979–5987 https://doi.org/10.1021/jf3001197 Taktak, W., Nasri, R., Hamdi, M., Gomez-Mascaraque, L G., Lopez-Rubio, A., Li, S., Nasri, M., & Karra-Chaâbouni, M (2018) Physicochemical, textural, rheological and microstructural properties of protein isolate gels produced from European eel (Anguilla anguilla) by heat-induced gelation process Food Hydrocolloids, 82, 278–287 https://doi.org/10.1016/j.foodhyd.2018.04.008 Tao, Z., Nakano, T., Yamaguchi, T., & Sato, M (n.d.) diffusion of histamine in the muscle of scombroid fishes Tohoku University , Graduate School of Agricultural Science , Laboratory Biochemistry , Sendai 981-8555 , JAPAN ( tzhh@bios.tohoku.ac.jp ) of Marine Distribution and situation of bacterium in the mi 1394–1397 Taylor, S L., Kabourek, J L., & Hefle, S L (2004) Fish allergy: Fish and products thereof Journal of Food Science, 69(8), 175–180 https://doi.org/10.1111/j.17503841.2004.tb18022.x Thawornchinsombut, S., & Park, J A E W (2006) Effect of NaCl on gelation characteristics of acid- and alkali-treated Pacific whiting fish protein isolates Journal of Food Biochemistry, 31(503), 427–455 Thomas, S N (2010) Coastal Fishery Resources of India Co n F V 1jQM Society of Fisheries Technologists, 1, 1–8 Tian, Y., Wang, W., Yuan, C., Zhang, L., Liu, J., & Liu, J (2017) Nutritional and Digestive Properties of Protein Isolates Extracted from the Muscle of the Common Carp Using pH-Shift Processing Journal of Food Processing and Preservation, 41(1) https://doi.org/10.1111/jfpp.12847 Tokur, B., & Korkmaz, K (2007) The effects of an iron-catalyzed oxidation system on lipids and proteins of dark muscle fish Food Chemistry, 104(2), 754–760 https://doi.org/10.1016/j.foodchem.2006.12.033 Torres, J A., Rodrigo-García, J., Jaczynski, J., & Chen, Y C (2006) ecovery of byproducts from seafood processing streams Maximising the Value of Marine By70 Products, 65–90 https://doi.org/10.1533/9781845692087.1.65 Turgeon, S L., & Laneuville, S I (2009) Protein + Polysaccharide Coacervates and Complexes From Scientific Background to their Application as Functional Ingredients in Food Products In Modern Biopolymer Science (First Edit) Elsevier Inc https://doi.org/10.1016/B978-0-12-374195-0.00011-2 Undeland, I., Kelleher, S D., & Hultin, H O (2002) Recovery of functional proteins from herring (Clupea harengus) light muscle by an acid or alkaline solubilization process Journal of Agricultural and Food Chemistry, 50(25), 7371–7379 https://doi.org/10.1021/jf020199u Wen, J., Arakawa, T., & Philo, J S (1996) Size-Exclusion Chromatography with OnLine Light-Scattering, Absorbance, and Refractive Index Detectors for Studying Proteins and Their Interactions:Review Polymer, 166, 155–166 Wongsagonsup, R., Shobsngob, S., Oonkhanond, B., & Varavinit, S (2005) Zeta potential (ζ) analysis for the determination of protein content in rice flour Starch/Staerke, 57(1), 25–31 https://doi.org/10.1002/star.200400307 Wu, L., Wu, T., Wu, J., Chang, R., Lan, X., Wei, K., & Jia, X (2016) Effects of cations on the “salt in” of myofibrillar proteins Food Hydrocolloids, 58, 179– 183 https://doi.org/10.1016/j.foodhyd.2016.02.028 Yongsawatdigul, J., & Park, J W (2004) (2004) Effects of alkali and acid solubilisation on gelation characteristics of rockfish muscle proteins Zhao, J., Dong, F., Li, Y., Kong, B., & Liu, Q (2015) Effect of freeze-thaw cycles on the emulsion activity and structural characteristics of soy protein isolate Process Biochemistry, 50(10), 1607–1613 https://doi.org/10.1016/j.procbio.2015.06.021 Zhong, S., Liu, S., Cao, J., Chen, S., Wang, W., & Qin, X (2016) Fish Protein Isolates Recovered from Silver Carp (Hypophthalmichthys molitrix) By-Products Using Alkaline pH Solubilization and Precipitation Journal of Aquatic Food Product Technology, 25(3), https://doi.org/10.1080/10498850.2013.865282 71 400–413 APPENDICES Appendices Content Page Test report of Amino acid in TDM II Test report of Amino acid in TDM III Test report of Amino acid in TDMPI IV Test report of Amino acid in TDMPI V Determination of histamine in TDM VI Determination of histamine in TDMPI VII Effect of pH ( NaOH) VIII I Appendix 1: Test report of Amino acid in TDM II Appendix 2: Test report of Amino acid in TDM III Appendix 3: Test report of Amino acid in TDMPI IV Appendix 4: Test report of Amino acid in TDMPI V Appendix 5: Determination of histamine in TDM VI Appendix 6: Determination of histamine in TDMPI VII Appendix 7: Effect of pH (using NaOH) pH Yield,% time time time Mean, % SD 6.52 5.83 7.19 6.52 0.55 10.83 9.95 10.54 10.44 0.37 10 24.85 25.37 26.82 25.68 0.83 11 39.82 41.56 42.82 41.40 1.23 12 57.24 56.15 57.81 57.07 0.69 12.6 51.78 51.20 53.29 52.09 0.88 VIII ...MINISTRY OF EDUCATION AND TRAINING NHA TRANG UNIVERSITY LAURINE MULE MUENI 60CH300 EXTRACTION AND CHARACTERIZATION OF FISH PROTEIN ISOLATE FROM YELLOWFIN (Thunnus albacares) DARK MUSCLE USING pH- SHIFT. .. Faculty of Graduate Studies: KHANH HOA - 2020 UNDERTAKING I undertake that the thesis entitled: ? ?Extraction and characterization of fish protein isolate from Yellowfin (Thunnus albacares) dark muscle. .. Objectives of the study General objective The overall aim of the work was to characterize the various pH- treated fish protein isolates extracted by pH- shift method from yellowfin dark tuna muscle

Ngày đăng: 17/02/2021, 21:05

TỪ KHÓA LIÊN QUAN

TÀI LIỆU CÙNG NGƯỜI DÙNG

TÀI LIỆU LIÊN QUAN