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Characterization of dual enzyme resulted from bicistronic expression of two β-glucanases in porcine cells |
ZHANG Xian-wei, LI Zi-cong, MENG Fan-ming, WANG De-hua, LIU De-wu, HE Xiao-yan, SUN Yue, BAI Yin-shan, WU Zhen-fang |
1、National Engineering Research Center for Breeding Swine Industry, South China Agricultural University, Guangzhou 510642,P.R.China
2、Wen’s Research Institute, Guangdong Wen’s Food Group Co. Ltd., Yunfu 527439, P.R.China |
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摘要 Many animal feed grains contain high β-glucan in the cell wall. Pigs do not secret β-glucanase to degrade the β-glucan in their feed. The indigestible β-glucan not only blocks the release of nutrients from the grain cell wall, but also increases the digesta viscosity in the gastrointestinal tract of pigs. Therefore, dietary β-glucan significantly inhibits nutrient digestion and absorption in pigs. Transgenic expression of β-glucanase in the digestive tract of pigs may offer a solution to solve this problem. In the current study, four arti?cial codon-optimized β-glucanases genes was prepared and expressed in porcine cells. Only pBgA and pEgx showed high activity in transfected pig kidney cells. To improve the pH range and pH stability of β-glucanase, the two β-glucanases, pBgA and pEgx, were co-expressed in pig kidney cells and salivary gland cells by Linker A3 or 2A peptide. The resulting dual enzymes of pBgA3pEg and pBg2ApEg showed significantly enlarged pH range and significantly increased pH stability, as compared to parental enzymes. These results provide useful data for future study on increasing the feed digestibility of pigs by transgenic expression of β-glucanase in their salivary glands.
Abstract Many animal feed grains contain high β-glucan in the cell wall. Pigs do not secret β-glucanase to degrade the β-glucan in their feed. The indigestible β-glucan not only blocks the release of nutrients from the grain cell wall, but also increases the digesta viscosity in the gastrointestinal tract of pigs. Therefore, dietary β-glucan significantly inhibits nutrient digestion and absorption in pigs. Transgenic expression of β-glucanase in the digestive tract of pigs may offer a solution to solve this problem. In the current study, four arti?cial codon-optimized β-glucanases genes was prepared and expressed in porcine cells. Only pBgA and pEgx showed high activity in transfected pig kidney cells. To improve the pH range and pH stability of β-glucanase, the two β-glucanases, pBgA and pEgx, were co-expressed in pig kidney cells and salivary gland cells by Linker A3 or 2A peptide. The resulting dual enzymes of pBgA3pEg and pBg2ApEg showed significantly enlarged pH range and significantly increased pH stability, as compared to parental enzymes. These results provide useful data for future study on increasing the feed digestibility of pigs by transgenic expression of β-glucanase in their salivary glands.
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Received: 12 February 2014
Accepted:
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Fund: This work was funded by a grant from the National Science and Technology Major Projects of China (2014ZX08006004) and three grants from the Department of Science and Technology of Guangdong, China (20111090700016, 2011A020102003 and 2011A020201009). |
Corresponding Authors:
WU Zhen-fang,Tel: +86-20-85280369, E-mail: wzfemail@163.com
E-mail: wzfemail@163.com
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About author: ZHANG Xian-wei, Tel: +86-766-2986345,E-mail: zxianw@163.com;* These authors contributed equally to this study. |
Cite this article:
ZHANG Xian-wei, LI Zi-cong, MENG Fan-ming, WANG De-hua, LIU De-wu, HE Xiao-yan, SUN Yue, BAI Yin-shan, WU Zhen-fang.
2015.
Characterization of dual enzyme resulted from bicistronic expression of two β-glucanases in porcine cells. Journal of Integrative Agriculture, 14(4): 732-740.
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Ao X, Meng Q W, Yan L, Kim H J, Hong S M, Cho J H, Kim IH. 2010. Effects of non-starch polysaccharide-degradingenzymes on nutrient digestibility, growth performance andblood profiles of growing pigs fed a diet based on corn andsoybean meal. Asian-Australia Journal Animal Science,23, 1632-1638Asan M, Ozcan N 2007. Expression of the β-(1,3-1,4)-glucanase gene in Streptococcus salivarius subsp.thermophilus. The Turkish Journal of Veterinary and AnimalSciences, 5, 319-324Bai Y, Wang J, Zhang Z, Shi P, Luo H, Huang H, Luo C, Yao B.2010. Expression of an extremely acidic beta-1,4-glucanasefrom thermoacidophilic Alicyclobacillus sp. A4 in Pichiapastoris is improved by truncating the gene sequence.Microbial Cell Factories, 9, 33.Deng W, Yang D, Zhao B, Ouyang Z, Song J, Fan N, Liu Z,Zhao Y, Wu Q, Nashun B, Tang J, Wu Z, Gu W, Lai L. 2011.Use of the 2A peptide for generation of multi-transgenicpigs through a single round of nuclear transfer. PLoS One,6, e19986.Fang Z F, Peng J, Liu Z L, Liu Y G. 2007. Responses of nonstarchpolysaccharide-degrading enzymes on digestibilityand performance of growing pigs fed a diet based on corn,soya bean meal and Chinese double-low rapeseed meal.Journal of Animal Physiology and Animal Nutrition, 91,361-368Forsberg C W, Meidinger R G, Liu M, Cottrill M, Golovan S,Phillips J P. 2013. Integration, stability and expression ofthe E. coli phytase transgene in the Cassie line of YorkshireEnviropigTM. Transgenic Research, 22, 379-389Golovan S P, Hayes M A, Phillips J P, Forsberg C W. 2001.Transgenic mice expressing bacterial phytase as a modelfor phosphorus pollution control. Nature Biotechnology,19, 429-433Golovan S P, Meidinger R G, Ajakaiye A, Cottrill M, WiederkehrM Z, Barney D J, Plante C, Pollard, J W, Fan M Z, Hayes MA, Laursen J, Hjorth J P, Hacker R R, Phillips J P, ForsbergC W. 2001. Pigs expressing salivary phytase produce lowphosphorusmanure. Nature Biotechnology, 19, 741-745Hua C, Yi H, Jiao L. 2011. Cloning and expression of theendo-1,3(4)-beta-glucanase gene from Paecilomyces sp.FLH30 and characterization of the recombinant enzyme.Bioscience Biotechnology & Biochemistry, 75, 1807-1812Inborr J, Schmitz M, Ahrens F. 1993. Effect of adding fibre andstarch degrading enzymes to a barley/wheat based diet onperformance and nutrient digestibility in different segmentsof the small intestine of early weaned pigs. Animal FeedScience and Technology, 44, 113-127Irshad M, Zahid A, Amber A. 2012. Characterization of Exo-1,4-β-glucanase produced from Trichoderma viridi throughsolid-state bio-processing of orange peel waste. Advancesin Bioscience and Biotechnology, 3, 580-584Jin X, Meng N, Xia L M. 2011. Expression of an endo-beta-1,4-glucanase gene from Orpinomyces PC-2 in Pichia pastoris.International Journal of Molecular Sciences, 12, 3366-3380Kreiss P, Cameron B, Rangara R, Mailhe P, Aguerre-CharriolO, Airiau M, Scherman D, Crouzet J, Pitard J. 1999. PlasmidDNA size does not affect the physicochemical properties oflipoplexes but modulates gene transfer efficiency. NucleicAcids Research, 27, 3792-3798Kong C, Adeola O. 2012. Supplementation of barley-baseddiets with beta-glucanase for pigs: Energy and amino aciddigestibility response. Journal of Animal Science, 90, 74-76Lei X G, Ku P K, Miller E R, Yokoyama M T. 1993. Supplementingcorn-soybean meal diets with microbial phytase linearlyimproves phytate phosphorus utilization by weanling pigs.Journal of Animal Science, 71, 3359-3367Li S, Sauer W C, Huang S X, Gabert V M. 1996. Effect of betaglucanasesupplementation to hulless barley- or wheatsoybeanmeal diets on the digestibilities of energy, protein,beta-glucans, and amino acids in young pigs. Journal ofAnimal Science, 74, 1649-1656Li Z, Michael I P, Zhou D, Nagy A, Rini J M. 2013. SimplepiggyBac transposon-based mammalian cell expressionsystem for inducible protein production. Proceedings ofthe National Academy of Sciences of the United States ofAmerica, 110, 5004-5009Loprete D M, Hill T W. 2002. Isolation and characterizationof an endo-(1,4)-{beta}-glucanase secreted by Achlya ambisexualis. Mycologia, 94, 903-911Lu P, Feng M G, Li W F, Hu C X. 2006. Construction andcharacterization of a bifunctional fusion enzyme of Bacillussourcedbeta-glucanase and xylanase expressed inEscherichia coli. Federation of European MicrobiologicalSocieties, 261, 224-230Lu P, Feng M G. 2008. Bifunctional enhancement of a betaglucanase-xylanase fusion enzyme by optimization ofpeptide linkers. Applied Microbiology and Biotechnology,79, 579-587Luo H, Yang J, Yang P, Li J, Huang H, Shi P, Bai Y, Wang Y,Fan Y, Yao B. 2010. Gene cloning and expression of anew acidic family 7 endo-beta-1,3-1,4-glucanase from theacidophilic fungus Bispora sp. MEY-1. Applied Microbiologyand Biotechnology, 85, 1015-1023Mathlouthi N, Juin H, Larbier M. 2003. Effect of xylanase andbeta-glucanase supplementation of wheat- or wheat- andbarley-based diets on the performance of male turkeys.British Poultry Science, 44, 291-298Meidinger R G, Ajakaiye A, Fan M Z, Zhang J, Phillips J P,Forsberg C W. 2013. Digestive utilization of phosphorusfrom plant-based diets in the Cassie line of transgenicYorkshire pigs that secrete phytase in the saliva. Journalof Animal Science, 91, 1307-1320Merchant H A, McConnell E L, Liu F, Ramaswamy C,Kulkarni R P, Basit A W, Murdan S. 2011. Assessmentof gastrointestinal pH, fluid and lymphoid tissue in theguinea pig, rabbit and pig, and implications for their use indrug development. European Journal of PharmaceuticalSciences, 42, 3-10Miller G L. 1959. Use of dinitrosalicylic acid reagent fordetermination of reducing sugar. Analytical Chemistry, 31,426-428Omogbenigun F O, Nyachoti C M, Slominski B A. 2004. Dietarysupplementation with multienzyme preparations improvesnutrient utilization and growth performance in weaned pigs.Journal of Animal Sciences, 82, 1053-1061Owusu-Asiedu A, Simmins P H, Brufau J, Lizardo R, PéronA. 2010. Effect of xylanase and β-glucanase on growthperformance and nutrient digestibility in piglets fed wheatbarley-based diets. Livestock Science, 134, 76-78Roongsawang N, Peerada P, Minradee W, Warasirin S,Puseenam A, Lily E, Tanapongpipat S. 2010. Coexpressionoffungal phytase and xylanase utilizing the cis-actinghydrolase element in Pichia pastoris. FEMS YeastResearch, 10, 909-916Schulze H, van Leeuwen P, Verstegen M W, Huisman J,Souffrant W B, Ahrens F. 1994. Effect of level of dietaryneutral detergent fiber on ileal apparent digestibility andileal nitrogen losses in pigs. Journal of Animal Science,72, 2362-2368Teng D, Wang J H, Fan Y, Yang Y L, Tian Z G, Luo J, YangG P, Zhang F. 2006. Cloning of beta-1,3-1,4-glucanasegene from Bacillus licheniformis EGW039 (CGMCC 0635)and its expression in Escherichia coli BL21 (DE3). AppliedMicrobiology and Biotechnology, 72, 705-712De Vries S, Pustjens A M, Schols H A, Hendriks W H, GerritsW J J. 2012. Improving digestive utilization of fiber-richfeedstuffs in pigs and poultry by processing and enzymetechnologies: A review. Animal Feed Science andTechnology, 178, 123-138Whyte J W R J, Samuel J Z M, Prather K D W R. 2010.Optimization of square-wave electroporation for transfectionof porcine fetal fibroblasts. Transgenic Research, 19,611-620Willamil J, Badiola I, Devillard E, Geraert P A, Torrallardona D.2012. Wheat-barley-rye or corn-fed growing pigs responddifferently to dietary supplementation with a carbohydrasecomplex. Journal of Animal Science, 90, 824-832Wu Y, Fan C, Li Y. 2009. Protein purification involving a uniqueauto-cleavage feature of a repeated EAAAK peptide.Journal of Chromatography (B), 877, 4015-4021Wurm F M. 2004. Production of recombinant protein therapeuticsin cultivated mammalian cells. Nature Biotechnology, 22,1393-1398Yin H F, Fan B L, Yang B, Liu Y F, Luo J, Tian X H, Li N.2006. Cloning of pig parotid secretory protein geneupstream promoter and the establishment of a transgenicmouse model expressing bacterial phytase for agriculturalphosphorus pollution control. Journal of Animal Science,84, 513-519 |
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