Partial characterization, quantification and activity of pancreatic lipase in the gastrointestinal tract of Totoaba macdonaldi

Authors

  • Mayra L. González-Félix Department of Scientific and Technological Research, University of Sonora, Edificio 7-G, Blvd. Luis Donaldo Colosio s/n, e/Sahuaripa y Reforma, Col. Centro, C.P. 83000, Hermosillo, Sonora
  • Edna B. Santana-Bejarano Department of Scientific and Technological Research, University of Sonora, Edificio 7-G, Blvd. Luis Donaldo Colosio s/n, e/Sahuaripa y Reforma, Col. Centro, C.P. 83000, Hermosillo, Sonora
  • Martin Perez-Velazquez Department of Scientific and Technological Research, University of Sonora, Edificio 7-G, Blvd. Luis Donaldo Colosio s/n, e/Sahuaripa y Reforma, Col. Centro, C.P. 83000, Hermosillo, Sonora http://orcid.org/0000-0002-9019-1220
  • Ana G. Villalba-Villalba Department of Physics, University of Sonora, Edificio 3-R, Blvd. Luis Encinas y Rosales s/n, Col. Centro, C.P. 83000, Hermosillo, Sonora

Keywords:

Totoaba macdonaldi, pancreatic lipase, enzymatic activity, gastrointestinal tract, lipids

Abstract

Paper description:

  • Pancreatic lipase is one of the main enzymes in higher vertebrates. It participates in the digestion of dietary lipid, one of the crucial macronutrients.
  • Knowledge of the type of lipase present in a particular fish species and its functional characteristics can contribute to the understand of its digestive physiology. This type of knowledge has not been advanced significantly for cultured fish species of commercial importance.
  • Totoaba macdonaldi has great potential as a candidate species for aquaculture. Studying the enzymatic action and potential of its pancreatic lipase will contributes to a better understanding of lipid catabolism which could help improve formulations of balanced feeds.


Abstract: Lipids are one of the main macronutrients that constitute balanced feeds used in aquaculture. Adequate utilization of dietary lipid is influenced by the activity of pancreatic lipase, one of the enzymes that promotes digestion of dietary lipids in the gastrointestinal tract of fish. The culture of Totoaba macdonaldi is quite recent; its nutritional requirements have been partially established. Knowing the characteristics of pancreatic lipase for this species could help optimize the dietary lipids included in balanced feeds for its culture. Therefore, the aim of this work is to partially characterize and evaluate the enzymatic activity of pancreatic lipase for T. macdonaldi. Biological indices showed that experimental organisms had a good nutritional status. Pancreatic lipase molecular weight was determined by native sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) and its activity was evaluated in crude enzymatic extracts from different gastrointestinal tract regions. The molecular weight of lipase was estimated to be 70.4 kDa; the highest lipolytic activity was observed at 45°C and at a pH optimum of 8.0 in the anterior intestine and pyloric caeca, where the concentration and activity of the enzyme was significantly higher (P=0.004) compared to the distal parts of the intestine. Biochemical characteristics observed for the pancreatic lipase of T. macdonaldi are quite similar to other lipases of fish cultured worldwide; results provided in this study will help understand the role this lipolytic enzyme plays in the digestive process of this species.

https://doi.org/10.2298/ABS180202009G

Received: February 2, 2018; Revised: March 16, 2018; Accepted: March 16, 2018; Published online: March 21, 2018

How to cite this article: González-Félix ML, Santana-Bejarano EB, Perez-Velazquez M, Villalba-Villalba AG. Partial characterization, quantification and activity of pancreatic lipase in the gastrointestinal tract of Totoaba Macdonaldi. Arch Biol Sci. 2018;70(3):…

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References

Patton JS, Nevenzel JC, Benson AA. Specificity of digestive lipases in hydrolysis of wax esters and triglycerides studied in anchovy and other selected fish. Lipids. 1975;10:575-83.

Lowe ME. Structure and function of pancreatic lipase and colipase. Annu Rev Nutr. 1997;17:141-58.

Lowe ME. The triglyceride lipases of the pancreas. J Lipid Res. 2002;43:2007-16.

Van Tilbeurgh H, Bezzine S, Cambillau C, Verger R, Carrière F. Colipase: structure and interaction with pancreatic lipase. Biochim Biophys Acta. 1999;1441:173-84.

Crenon I, Foglizzo E, Kerfelec B, Verine A, Pignol D, Hermoso J, Bonicel J, Chapus C. Pancreatic lipase-related protein type I: A specialized lipase or an inactive enzyme. Protein Eng. 1998;11:135-42.

Terzyan S, Wang Ch-S, Downs D, Hunter B, Zhang X. Crystal structure of the catalytic domain of human bile salt activated lipase. Protein Sci. 2000;9:1783-90.

Kurtovic I, Marshall SN, Zhao X, Simpson BK. Lipases from mammals and fishes. Rev Fish Sci. 2009;17:18-40.

Holmes RS, Cox LA. Bioinformatics and evolution of vertebrate pancreatic lipase and related proteins and genes. J Data Mining in Genom Proteomics. 2012;3:1-10.

Leger C. Digestion, absorption and transport of lipids. In: Cowey CB, Mackie AM, Bell JG, editors. Nutrition and feeding of fish. Academic Press, London, UK; 1985. p. 299-331.

Patton JS, Haswell MS, Moon TW. Aspects of lipid synthesis, hydrolysis, and transport studied in selected Amazon fish. Can J Zool. 1978;56:787-92.

Mukundan MK, Gopakumar K, Nair MR. Purification of a lipase from the hepatopancreas of oil sardine (Sardinella longiceps Linnaeus) and its characteristics and properties. J Sci Food Agric. 1985;36:191-203.

Tocher DR, Sargent JR. Studies on triacylglycerol, wax ester and sterol ester hydrolases in intestinal caeca of rainbow trout (Salmo gairdneri, L.) fed diets rich in triacylglycerols and was esters. Comp Biochem Physiol. 1984;77:561-71.

Izquierdo MS, Henderson RJ. The determination of lipase and phospholipase activities in gut contents of turbot (Scophthalmus maximus) by fluorescence-based assays. Fish Physiol Biochem. 1998;19:153-62.

Koven WM, Henderson RJ, Sargent JR. Lipid digestion in turbot (Scophthalmus maximus) I: Lipid class and fatty acid composition of digesta from different segments of the digestive tract. Fish Physiol Biochem. 1994;13:69-79.

Koven WM, Henderson RJ, Sargent JR. Lipid digestion in turbot (Scophthalmus maximus) II: Lipolysis in vitro of 14C-labelled triacylglycerol, cholesterol ester and phosphatidylcholine by digesta from different segments of the digestive tract. Fish Physiol Biochem. 1994;13:275-83.

Hoehne-Reitan K, Kjørsvik E, Gjellesvik DR. Development of bile salt-dependent lipase in larval turbot. J Fish Biol. 2001;58:737-45.

Hoehne-Reitan K, Kjørsvik E, Reitan KI. Bile salt-dependent lipase in larval turbot, as influenced by density and lipid content of prey. J Fish Biol. 2001;58:746-54.

González-Félix ML, Minjarez-Osorio C, Perez-Velazquez M, Urquidez-Bejarano P. Influence of dietary lipid on growth performance and body composition of the Gulf corvina, Cynoscion othonopterus. Aquaculture. 2015;448:401-9.

Tocher DR. Metabolism and functions of lipids and fatty acids in teleost fish. Rev Fish Sci. 2003;11:107-84.

Halver JE, Hardy RW. Fish Nutrition. Elsevier Sciences. 3er edition. Orlando, Florida, USA; 2002. 353 p.

Bromley PJ. Effect of dietary protein, lipid and energy content on the growth of turbot Scopthalmus maximus. Aquaculture. 1980;19:359-69.

Hillestad M, Johnsen F. High-energy⁄low-protein diets for Atlantic salmon: effects on growth, nutrient retention and slaughter quality. Aquaculture. 1994;124:109-16.

Ellis SC, Reigh RC. Effects of dietary lipid and carbohydrate levels on growth composition of juvenile red drum Sciaenops ocellatus. Aquaculture. 1991;97:383-94.

McGoogan BB, Gatlin DM III. Dietary manipulations affecting growth and nitrogenous waste production of red drum Sciaenops ocellatus. I. Effects of dietary protein and energy levels. Aquaculture. 1999;178:333-48.

Rueda-López S, Lazo JP, Correa-Reyes G, Viana MT. Effect of dietary protein and energy levels on growth, survival and body composition of juvenile Totoaba macdonaldi. Aquaculture. 2011;319:385-90.

Ricker WE. Computation and interpretation of biological statistics of fish populations. B Fish Res Board Can. 1975;191:1-382.

Association of Official Analytical Chemists (AOAC). Official Methods of Analysis. Association of Analytical Chemists, Arlington, VA, USA; 2005.

Singh R, Gupta VK, Goswami VK. A simple activity staining protocol for lipases and esterases. App Microbiol Biotechnol. 2006;70:679-82.

Shiau SY, Lan CW. Optimum dietary protein level and protein to energy ratio for growth of grouper (Epinephelus malabaricus). Aquaculture. 1996;145:259-66.

Thoman ES, Davis DA, Arnold CR. Evaluation of growout diets with varying protein and energy levels for red drum (Sciaenops ocellatus). Aquaculture. 1999;176:343-53.

Hixson SE. Fish nutrition and current issues in aquaculture: The balance in providing safe and nutrious seafood, in an environmentally sustainable manner. J Aquac Res Dev. 2014;5:1-10.

Perez-Velazquez M., Minjarez-Osorio C., González-Félix ML. Effect of dietary lipid level on growth performance, feed utilization, and body composition of totoaba, Totoaba macdonaldi (Gilbert, 1890). Aquacult Res. 2017;48:2607-17.

Zambonino-Infante JL, Cahu CL. High dietary lipid levels enhance digestive tract maturation and improve Dicentrarchus labrax larval development. J Nutr. 1999;129:1195-200.

Buchet V, Zambonino-Infante JL, Cahu CL. Effect of lipid level in a compound diet on the development of red drum (Sciaenops ocellatus) larvae. Aquaculture. 2000;184:339-47.

Görgün S, Akpinar MA. Purification and characterization of lipase from the liver of carp, Cyprinus carpio L. (1758), living in Lake Tödürge (Sivas, Türkiye). Turk J Fish Aquat Sci. 2012;12:207-15.

Iijima N, Tanaka S, Ota Y. Purification and characterization of bile salt-activated lipase from the hepatopancreas of red sea bream, Pagrus major. Fish Physiol Biochem. 1998;18:59-69.

Gjellesvik DR, Lombardo D, Walther BT. Pancreatic bile salt dependent lipase from cod (Gadus morhua): purification and properties. Biochim Biophys Acta. 1992;1124:123-34.

Kurtovic I, Marshall SN, Zhao X. Purification and properties of digestive lipases from Chinook salmon (Oncorhynchus tshawytscha) and zeland hoki (Macruronus novaezelandiae). Fish Physiol Biochem. 2010;36:1041-60.

Rueda-López S, Martínez-Montaño E, Viana MT. Biochemical characterization and comparison of pancreatic lipases from the Pacific bluefin tuna, Thunnus orientalis; totoaba, Totoaba macdonaldi; and striped bass, Morone saxatilis. J World Aquacult Soc. 2017;48:156-65.

Deguara S, Jauncey K, Agius C. Enzyme activities and pH variations in the digestive tract of gilthead sea bream. J Fish Biol. 2003;62:1033-43.

Nolasco H, Moyano LFJ, Vega-Villasante F. Partial characterization of pyloric-duodenal lipase of gilthead seabream (Sparus aurata). Fish Physiol Biochem. 2011;37:43-52.

Matus de la Parra A, Rosas A, Lazo JP, Viana MT. Partial characterization of the digestive enzymes of Pacific bluefin tuna Thunnus orientalis under culture conditions. Fish Physiol Biochem. 2007;33:223-31.

Xiong DM, Xie CX, Zhang HJ, Liu HP. Digestive enzymes along digestive tract of a carnivorous fish Glyptosternum maculatum (Sisoridae, Siluriformes). J Anim Physiol Anim Nutr. 2011;95:56-64.

Jun-Sheng L, Jian-Lin L, Ting-Ting W. Ontogeny of protease, amylase and lipase in the alimentary tract of hybrid juvenile tilapia (Oreochromis niloticus × Oreochromis aureus). Fish Physiol Biochem. 2006;32:295-303.

Rust MB. Nutritional Physiology. In: Halver JE and Hardy RW, editors. Fish Nutrition. Academic Press, New York, USA; 2002. p. 368-446.

Morais S, Conceição LEC, Rønnestad I, Koven W, Cahu C, Zambonino-Infante JL, Dinis MT. Dietary neutral lipid level and source in marine fish larvae: effects on digestive physiology and food intake. Aquaculture. 2007;268:106-22.

Lazo JP, Mendoza R, Holt GJ, Aguilera C, Arnold CR. Characterization of digestive enzymes during larval development of red drum (Sciaenops ocellatus). Aquaculture. 2007;265:194-205.

Noriega-Rodriguez JA, Gámez-Meza N, Alanis-Villa A, Medina-Juárez LA, Tejeda-Mansir A, Angulo-Guerrero O, García HS. Extraction and fractionation of lipolytic enzyme from viscera of Monterey sardine (Sardinops sagax caerulea). Int J Food Sci Technol. 2009;44:1223-28.

Grogan G. Practical biotransformations. A beginner’s guide. Wiley and Sons, Ltd. Cornwall, UK; 2009. 344 p.

Murray RK, Mayes PA, Granner DK, Rodwell VW. Enzyme kinetics. In: Rodwell, VW, editor. Harpers Biochemistry, Mc Graw Hill Inc., Mexico City, Mexico; 1990. p. 68-81.

Minjarez-Osorio C., González-Félix ML, Perez-Velazquez M. Biological performance of Totoaba macdonaldi in response to dietary protein level. Aquaculture. 2012;362-363:50-4.

Lizama MAP, Ambrosio AM. Condition factor in nine species of fish of the Characidae family in the upper Parana River Floodplain, Brazil. Braz J Biol. 2002;62:113-24.

Chaturvedi, J, Saksena DN. Diet composition, feeding intensity, gastrosomatic index and hepatosomatic index of a catfish, Mystus cavasius from Chambal river (near, Rajghat) Morena, Madhya Pradesh. Int J Recent Sci Res. 2013;4:1350-6.

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Published

2018-08-20

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González-Félix ML, Santana-Bejarano EB, Perez-Velazquez M, Villalba-Villalba AG. Partial characterization, quantification and activity of pancreatic lipase in the gastrointestinal tract of Totoaba macdonaldi. Arch Biol Sci [Internet]. 2018Aug.20 [cited 2024Dec.22];70(3):489-96. Available from: https://serbiosoc.org.rs/arch/index.php/abs/article/view/2617

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