Expression, characterization, and application potentiality evaluation of recombinant human-like collagen in Pichia pastoris

Lingling Ma , Xiaolin Liang , Shiqin Yu , Jingwen Zhou

Bioresources and Bioprocessing ›› 2022, Vol. 9 ›› Issue (1) : 119

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Bioresources and Bioprocessing ›› 2022, Vol. 9 ›› Issue (1) : 119 DOI: 10.1186/s40643-022-00606-3
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Expression, characterization, and application potentiality evaluation of recombinant human-like collagen in Pichia pastoris

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Abstract

Collagen is a biofunctional protein that has been widely used in many fields, including but not limited to biomedical, cosmetics and skin care, food, and novel materials. Recombinant collagen has great potential as an alternative to collagen extracted from animals because it avoids the immune response, and the yield and properties are stable. However, challenges remain in the industrial application of recombinant collagen, including improving the expression yield, reducing the cost of purification for industry and expanding applications. In this study, a cloning and recombination method was used to heterologously express the recombinant human-like collagen (RHLC) in Pichia pastoris GS115 using the pPIC9k expression vector. The RHLC expression titre was 2.33 g/L via a 5-L fermenter, and the purification was completed within 48 h and was 98% pure. The characteristics of RHLC were investigated. Furthermore, potential applications for RHLC were explored, such as basal collagen sponge preparation, forming films with chitosan and production of collagen hydrolysed peptides. RHLC has various potential applications due to its triple helical structure, thermostability, good biocompatibility and film-forming ability.

Keywords

Recombinant human-like collagen / Pichia pastoris / Potential applications

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Lingling Ma, Xiaolin Liang, Shiqin Yu, Jingwen Zhou. Expression, characterization, and application potentiality evaluation of recombinant human-like collagen in Pichia pastoris. Bioresources and Bioprocessing, 2022, 9(1): 119 DOI:10.1186/s40643-022-00606-3

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References

[1]

Ahmad M, Hirz M, Pichler H, Schwab H. Protein expression in Pichia pastoris: recent achievements and perspectives for heterologous protein production. Appl Microbiol Biotechnol, 2014, 98(12): 5301-5317.

[2]

Ahmad M, Nirmal NP, Danish M, Chuprom J, Jafarzedeh S. Characterisation of composite films fabricated from collagen/chitosan and collagen/soy protein isolate for food packaging applications. RSC Adv, 2016, 6(85): 82191-82204.

[3]

Ahmed M, Verma AK, Patel R. Collagen extraction and recent biological activities of collagen peptides derived from sea-food waste: a review. Sustain Chem Pharm, 2020, 18: 100315.

[4]

Andonegi M, Heras KL, Santos-Vizcaino E, Igartua M, Hernandez RM, de la Caba K, Guerrero P. Structure-properties relationship of chitosan/collagen films with potential for biomedical applications. Carbohydr Polym, 2020, 237.

[5]

Asghari F, Samiei M, Adibkia K, Akbarzadeh A, Davaran S. Biodegradable and biocompatible polymers for tissue engineering application: a review. Artif Cells Nanomed Biotechnol, 2017, 45(2): 185-192.

[6]

Bahrami N, Nouri Khorasani S, Mahdavi H, Khalili S. Layer-by-layer self-assembly of collagen and chitosan biomolecules on polyurethane films. J Appl Polym Sci, 2020, 137(45): 49417.

[7]

Becerra J, Rodriguez M, Leal D, Noris-Suarez K, Gonzalez G. Chitosan-collagen-hydroxyapatite membranes for tissue engineering. J Mater Sci Mater Med, 2022, 33(2): 18.

[8]

Bettini S, Bonfrate V, Syrgiannis Z, Sannino A, Salvatore L, Madaghiele M, Valli L, Giancane G. Biocompatible collagen paramagnetic scaffold for controlled drug release. Biomacromol, 2015, 16(9): 2599-2608.

[9]

Bhuimbar MV, Bhagwat PK, Dandge PB. Extraction and characterization of acid soluble collagen from fish waste: development of collagen-chitosan blend as food packaging film. J Environ Chem Eng, 2019, 7(2): 102983.

[10]

Bisht M, Martins M, Dias ACRV, Ventura SPM, Coutinho JAP. Uncovering the potential of aqueous solutions of deep eutectic solvents on the extraction and purification of collagen type I from Atlantic codfish (Gadusmorhua). Green Chem, 2021, 23(22): 8940-8948.

[11]

Brodsky B, Persikov AV. Molecular structure of the collagen triple helix. Adv Protein Chem, 2005, 70: 301-339.

[12]

Choi KH, Yoon JW, Kim M, Lee HJ, Jeong J, Ryu M, Jo C, Lee CK. Muscle stem cell isolation and in vitro culture for meat production: a methodological review. Compr Rev Food Sci Food Saf, 2021, 20(1): 429-457.

[13]

Correia C, Sousa RO, Vale AC, Peixoto D, Silva TH, Reis RL, Pashkuleva I, Alves NM. Adhesive and biodegradable membranes made of sustainable catechol-functionalized marine collagen and chitosan. Colloids Surf B Biointerfaces, 2022, 213.

[14]

Oliveira VDM, Assis CRD, Costa BDAM, Neri RCDA, Monte FTD, Freitas HMSDCV, França RCP, Santos JF, Bezerra RDS, Porto ALF. Physical, biochemical, densitometric and spectroscopic techniques for characterization collagen from alternative sources: a review based on the sustainable valorization of aquatic by-products. J Mol Str, 2021, 1224.

[15]

DeFrates KG, Moore R, Borgesi J, Lin G, Mulderig T, Beachley V, Hu X. Protein-based fiber materials in medicine: a review. Nanomaterials, 2018, 8(7): 457.

[16]

Dong C, Lv Y. Application of collagen scaffold in tissue engineering: recent advances and new perspectives. Polymers, 2016, 8(2): 1-20.

[17]

Ebhodaghe SO. Natural polymeric scaffolds for tissue engineering applications. J Biomater Sci Polym Ed, 2021

[18]

Fan D, Duan M, Mi Y, Song J, Hui J, Wang D, Wang G. High density fermentation of recombinant E. coli for production of human-like collagen. J Chem Ind Eng (china), 2002, 53(7): 752-754.

[19]

Feng M, Betti M. Transepithelial transport efficiency of bovine collagen hydrolysates in a human Caco-2 cell line model. Food Chem, 2017, 224: 242-250.

[20]

Feng X, Zhang X, Li S, Zheng Y, Shi X, Li F, Guo S, Yang J. Preparation of aminated fish scale collagen and oxidized sodium alginate hybrid hydrogel for enhanced full-thickness wound healing. Int J Biol Macromol, 2020, 164: 626-637.

[21]

Fidler AL, Boudko SP, Rokas A, Hudson BG. The triple helix of collagens—an ancient protein structure that enabled animal multicellularity and tissue evolution. J Cell Sci, 2018, 131(7): jcs203950.

[22]

Gaspar-Pintiliescu A, Stanciuc AM, Craciunescu O. Natural composite dressings based on collagen, gelatin and plant bioactive compounds for wound healing: a review. Int J Biol Macromol, 2019, 138: 854-865.

[23]

Gellermann P, Schneider-Barthold C, Bolten SN, Overfelt E, Scheper T, Pepelanova I. Production of a recombinant non-hydroxylated gelatin mimetic in Pichia pastoris for biomedical applications. J Funct Biomater, 2019, 10(3): 1-12.

[24]

Ghorbani M, Nezhad-Mokhtari P, Ramazani S. Aloe vera-loaded nanofibrous scaffold based on zein/polycaprolactone/collagen for wound healing. Int J Biol Macromol, 2020, 153: 921-930.

[25]

Gibney R, Patterson J, Ferraris E. High-resolution bioprinting of recombinant human collagen type III. Polymers, 2021, 13(17): 1-17.

[26]

Gomes V, Salgueiro SP. From small to large-scale: a review of recombinant spider silk and collagen bioproduction. Discover Mater, 2022, 2(1): 1-24.

[27]

He Y, Hou Z, Wang J, Wang Z, Li X, Liu J, Liang Q, Zhao J. Assessment of biological properties of recombinant collagen-hyaluronic acid composite scaffolds. Int J Biol Macromol, 2020, 149: 1275-1284.

[28]

He Y, Wang J, Si Y, Wang X, Deng H, Sheng Z, Li Y, Liu J, Zhao J. A novel gene recombinant collagen hemostatic sponge with excellent biocompatibility and hemostatic effect. Int J Biol Macromol, 2021, 178: 296-305.

[29]

Heras R, Gavara R, Hernández-Muñoz P. Responsive packaging based on imine-chitosan films for extending the shelf-life of refrigerated fresh-cut pineapple. Food Hydrocoll, 2022

[30]

Hong H, Fan H, Chalamaiah M, Wu J. Preparation of low-molecular-weight, collagen hydrolysates (peptides): current progress, challenges, and future perspectives. Food Chem, 2019, 301.

[31]

Hou W, Fan D, Xue W, Zhang W, Yu Q. Expression and purification of the recombinant human-like collagen II in E. coli. Chin J Pharm, 2006, 37(7): 454-457.

[32]

Irawan V, Sung TC, Higuchi A, Ikoma T. Collagen scaffolds in cartilage tissue engineering and relevant approaches for future development. Tissue Eng Regen Med, 2018, 15(6): 673-697.

[33]

Jabaiah A, Wang X, Raman SK, Ragan R, Da Silva NA, Wang SW. Nanoscale architecture and cellular adhesion of biomimetic collagen substrates. J Biomater Appl, 2014, 28(9): 1354-1365.

[34]

Jafari Sanjari A, Asghari M. A review on chitosan utilization in membrane synthesis. ChemBioEng Reviews, 2016, 3(3): 134-158.

[35]

Jaques A, Sánchez E, Orellana N, Enrione J, Acevedo CA. Modelling the growth of in-vitro meat on microstructured edible films. J Food Eng, 2021, 307: 1-8.

[36]

Jiang X, Wang Y, Fan D, Zhu C, Liu L, Duan Z. A novel human-like collagen hemostatic sponge with uniform morphology, good biodegradability and biocompatibility. J Biomater Appl, 2017, 31(8): 1099-1107.

[37]

Jiang S, Yu Z, Zhang L, Wang G, Dai X, Lian X, Yan Y, Zhang L, Wang Y, Li R, Zou H. Effects of different aperture-sized type I collagen/silk fibroin scaffolds on the proliferation and differentiation of human dental pulp cells. Regen Biomater, 2021, 8(4): 1-9.

[38]

Li L, Fan D, Ma X, Deng J, He J. High-level secretory expression and purification of unhydroxylated human collagen alpha1(III) chain in Pichia pastoris GS115. Biotechnol Appl Biochem, 2015, 62(4): 467-475.

[39]

Lin Z, Wu T, Wang W, Li B, Wang M, Chen L, Xia H, Zhang T. Biofunctions of antimicrobial peptide-conjugated alginate/hyaluronic acid/collagen wound dressings promote wound healing of a mixed-bacteria-infected wound. Int J Biol Macromol, 2019, 140: 330-342.

[40]

Lu X, Huang Y, Qu Y, Zhang Y, Zhang Z. Integrated transcriptomic and proteomic study on the different molecular mechanisms of PC12 cell growth on chitosan and collagen/chitosan films. Regen Biomater, 2020, 7(6): 553-565.

[41]

Mahendiran B, Muthusamy S, Sampath S, Jaisankar SN, Selvakumar R, Krishnakumar GS (2022) In vitro and in vivo biocompatibility of decellularized cellulose scaffolds functionalized with chitosan and platelet rich plasma for tissue engineering applications. Int J Biol Macromol 217:522–535. https://doi.org/10.1016/j.ijbiomac.2022.07.052

[42]

Myllyharju J, Nokelainen M, Vuorela A, Kivirikko KI. Expression of recombinant human type I-III collagens in the yeast Pichia pastoris. Biochem Soc Trans, 2000, 28(4): 353-357.

[43]

Nokelainen M, Tu H, Vuorela A, Notbohm H, Kivirikko KI, Myllyharju J. High-level production of human type I collagen in the yeast Pichia pastoris. Yeast, 2001, 18(9): 797-806.

[44]

Nöt LG, Naumov I, Vámhidy L, Lőrinczy D, Wiegand N. Comparison of thermal characteristics of degenerated and inflamed human collagen structures with differential scanning calorimetry. J Therm Anal Calorim, 2012, 113(1): 273-279.

[45]

Ocak B. Development of novel collagen hydrolysate bio-nanocomposite films extracted from hide trimming wastes reinforced with chitosan nanoparticles. Environ Sci Pollut Res Int, 2021, 28(26): 35145-35156.

[46]

Pakkanen O, Pirskanen A, Myllyharju J. Selective expression of nonsecreted triple-helical and secreted single-chain recombinant collagen fragments in the yeast Pichia pastoris. J Biotechnol, 2006, 123(2): 248-256.

[47]

Pandini FE, Kubo FMM, Plepis AMG, Martins V, da Cunha MR, Silva VR, Hirota VB, Lopes E, Menezes MA, Pelegrine AA, Andrade TN, Iatecola A, Britto BDC, Fernandes VAR, Gameiro LFO, Correia RR, Teixeira ML, Duarte Junior G, Reis CHB, Pereira E, Buchaim DV, Pomini KT, Teixeira DB, Buchaim RL, Lourenco EA. In vivo study of nasal bone reconstruction with collagen, elastin and chitosan membranes in abstainer and alcoholic rats. Polymers (basel), 2022, 14(1): 188.

[48]

Que RA, Arulmoli J, Da Silva NA, Flanagan LA, Wang SW. Recombinant collagen scaffolds as substrates for human neural stem/progenitor cells. J Biomed Mater Res A, 2018, 106(5): 1363-1372.

[49]

Ruggiero F, Koch M. Making recombinant extracellular matrix proteins. Methods, 2008, 45(1): 75-85.

[50]

Ruottinen M, Bollok M, Kogler M, Neubauer A, Krause M, Hamalainen ER, Myllyharju J, Vasala A, Neubauer P. Improved production of human type II procollagen in the yeast Pichiapastoris in shake flasks by a wireless-controlled fed-batch system. BMC Biotechnol, 2008, 8: 33.

[51]

Salehi E, Daraei P, Arabi Shamsabadi A. A review on chitosan-based adsorptive membranes. Carbohydr Polym, 2016, 152: 419-432.

[52]

Salvatore L, Gallo N, Aiello D, Lunetti P, Barca A, Blasi L, Madaghiele M, Bettini S, Giancane G, Hasan M, Borovkov V, Natali ML, Campa L, Valli L, Capobianco L, Napoli A, Sannino A. An insight on type I collagen from horse tendon for the manufacture of implantable devices. Int J Biol Macromol, 2020, 154: 291-306.

[53]

Sivaraman K, Shanthi C. Role of fish collagen hydrolysate in attenuating inflammation—an in vitro study. J Food Biochem, 2021, 45(9

[54]

Sorushanova A, Delgado LM, Wu Z, Shologu N, Kshirsagar A, Raghunath R, Mullen AM, Bayon Y, Pandit A, Raghunath M, Zeugolis DI. The collagen suprafamily: from biosynthesis to advanced biomaterial development. Adv Mater, 2019, 31(1): 1-39.

[55]

Stephens N, Di Silvio L, Dunsford I, Ellis M, Glencross A, Sexton A. Bringing cultured meat to market: technical, socio-political, and regulatory challenges in cellular agriculture. Trends Food Sci Technol, 2018, 78: 155-166.

[56]

Sun L, Xin F, Alper HS. Bio-synthesis of food additives and colorants-a growing trend in future food. Biotechnol Adv, 2021, 47: 1-20.

[57]

Teixeira LS, Feijen J, van Blitterswijk CA, Dijkstra PJ, Karperien M. Enzyme-catalyzed crosslinkable hydrogels: emerging strategies for tissue engineering. Biomaterials, 2012, 33(5): 1281-1290.

[58]

Valenzuela-Rojo RD, López-Cervantes J, Sánchez-Machado DI, Escárcega-Galaz AA, del Rosario Martínez-Macias M. Antibacterial, mechanical and physical properties of collagen–chitosan sponges from aquatic source. Sustain Chem Pharm, 2020, 15: 100218.

[59]

Vidal AR, Cansian RL, Mello RO, Demiate IM, Kempka AP, Dornelles RCP, Rodriguez JML, Campagnol PCB. Production of collagens and protein hydrolysates with antimicrobial and antioxidant activity from sheep slaughter by-products. Antioxidants (basel), 2022, 11(6): 1173.

[60]

Vuorela A, Myllyharju J, Nissi R, Pihlajaniemi T, Kivirikko KI. Assembly of human prolyl 4-hydroxylase and type III collagen in the yeast Pichia pastoris: formation of a stable enzyme tetramer requires coexpression with collagen and assembly of a stable collagen requires coexpression with prolyl 4-hydroxylase. EMBO J, 1997, 16(22): 6702-6712.

[61]

Wang L, Fan D, He J, Lv Z, Zhu C. A new strategy for secretory expression and mixed fermentation of recombinant human collagen α1 (III) chain in Pichia pastoris. Biotechnol Bioprocess Eng, 2014, 19(5): 916-924.

[62]

Wei B, Zhong H, Wang L, Liu Y, Xu Y, Zhang J, Xu C, He L, Wang H. Facile preparation of a collagen-graphene oxide composite: a sensitive and robust electrochemical aptasensor for determining dopamine in biological samples. Int J Biol Macromol, 2019, 135: 400-406.

[63]

Weinrich R, Strack M, Neugebauer F. Consumer acceptance of cultured meat in Germany. Meat Sci, 2020, 162: 1-6.

[64]

Williams DF. Challenges with the development of biomaterials for sustainable tissue engineering. Front Bioeng Biotechnol, 2019, 7: 1-10.

[65]

Worthen CA, Cui Y, Orringer JS, Johnson TM, Voorhees JJ, Fisher GJ. CD26 identifies a subpopulation of fibroblasts that produce the majority of collagen during wound healing in human skin. J Invest Dermatol, 2020, 140(12): 2515-2524.

[66]

Xiao J, Ma Y, Wang W, Zhang K, Tian X, Zhao K, Duan S, Li S, Guo Y. Incorporation of gelatin improves toughness of collagen films with a homo-hierarchical structure. Food Chem, 2021, 345: 1-9.

[67]

Yue C, Ding C, Du X, Wang Y, Su J, Cheng B. Self-assembly of collagen fibrils on graphene oxide and their hybrid nanocomposite films. Int J Biol Macromol, 2021, 193: 173-182.

[68]

Yu C, Ding C, Cheng B, Du X, Su J (2021b) Preparation of collagen/aspartic acid nanocomposite fibers and their self-assembly behaviors. J Nat Fibers, pp 1–12

[69]

Zarei M, Samimi A, Khorram M, Abdi MM, Golestaneh SI. Fabrication and characterization of conductive polypyrrole/chitosan/collagen electrospun nanofiber scaffold for tissue engineering application. Int J Biol Macromol, 2021, 168: 175-186.

[70]

Zhang H. Expression and purification of recombinant human collagen-like and its application in cosmetics, Vol. Master, 2017, Guangzhou: Jinan University.

[71]

Zhang Q, Fu R, Yao K, Jia D, He Q, Chi Y. Clarification effect of collagen hydrolysate clarifier on chrysanthemum beverage. Lwt-Food Sci Technol, 2018, 91: 70-76.

[72]

Zhang X, Adachi S, Ura K, Takagi Y. Properties of collagen extracted from Amur sturgeon Acipenserschrenckii and assessment of collagen fibrils in vitro. Int J Biol Macromol, 2019, 137: 809-820.

[73]

Zhang G, Zhao X, Li X, Du G, Zhou J, Chen J. Challenges and possibilities for bio-manufacturing cultured meat. Trends Food Sci Technol, 2020, 97: 443-450.

Funding

Natural Science Foundation of Jiangsu Province(BK20202002)

National Natural Science Foundation of China(32100024)

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