LAPSE:2023.1793
Published Article

LAPSE:2023.1793
as a Potential Biofactory for Antigens and Vehicle for Mucosal Application
February 21, 2023
Abstract
The demand for effective, low-cost vaccines increases research in next-generation biomanufacturing platforms and the study of new vaccine delivery systems (e.g., mucosal vaccines). Applied biotechnology in antigen production guides research toward developing genetic modification techniques in different biological models to achieve the expression of heterologous proteins. These studies are based on various transformation protocols, applied in prokaryotic systems such as Escherichia coli to eukaryotic models such as yeasts, insect cell cultures, animals, and plants, including a particular type of photosynthetic organisms: microalgae, demonstrating the feasibility of recombinant protein expression in these biological models. Microalgae are one of the recombinant protein expression models with the most significant potential and studies in the last decade. Unicellular photosynthetic organisms are widely diverse with biological and growth-specific characteristics. Some examples of the species with commercial interest are Chlamydomonas, Botryococcus, Chlorella, Dunaliella, Haematococcus, and Spirulina. The production of microalgae species at an industrial level through specialized equipment for this purpose allows for proposing microalgae as a basis for producing recombinant proteins at a commercial level. A specie with a particular interest in biotechnology application due to growth characteristics, composition, and protein production capacity is D. salina, which can be cultivated under industrial standards to obtain βcarotene of high interest to humans. D saline currently has advantages over other microalgae species, such as its growth in culture media with a high salt concentration which reduces the risk of contamination, rapid growth, generally considered safe (GRAS), recombinant protein biofactory, and a possible delivery vehicle for mucosal application. This review discusses the status of microalgae D. salina as a platform of expression of recombinant production for its potential mucosal application as a vaccine delivery system, taking an advance on the technology for its production and cultivation at an industrial level.
The demand for effective, low-cost vaccines increases research in next-generation biomanufacturing platforms and the study of new vaccine delivery systems (e.g., mucosal vaccines). Applied biotechnology in antigen production guides research toward developing genetic modification techniques in different biological models to achieve the expression of heterologous proteins. These studies are based on various transformation protocols, applied in prokaryotic systems such as Escherichia coli to eukaryotic models such as yeasts, insect cell cultures, animals, and plants, including a particular type of photosynthetic organisms: microalgae, demonstrating the feasibility of recombinant protein expression in these biological models. Microalgae are one of the recombinant protein expression models with the most significant potential and studies in the last decade. Unicellular photosynthetic organisms are widely diverse with biological and growth-specific characteristics. Some examples of the species with commercial interest are Chlamydomonas, Botryococcus, Chlorella, Dunaliella, Haematococcus, and Spirulina. The production of microalgae species at an industrial level through specialized equipment for this purpose allows for proposing microalgae as a basis for producing recombinant proteins at a commercial level. A specie with a particular interest in biotechnology application due to growth characteristics, composition, and protein production capacity is D. salina, which can be cultivated under industrial standards to obtain βcarotene of high interest to humans. D saline currently has advantages over other microalgae species, such as its growth in culture media with a high salt concentration which reduces the risk of contamination, rapid growth, generally considered safe (GRAS), recombinant protein biofactory, and a possible delivery vehicle for mucosal application. This review discusses the status of microalgae D. salina as a platform of expression of recombinant production for its potential mucosal application as a vaccine delivery system, taking an advance on the technology for its production and cultivation at an industrial level.
Record ID
Keywords
Dunaliella salina, mucosal, recombinant protein, vaccines
Subject
Suggested Citation
Castellanos-Huerta I, Gómez-Verduzco G, Tellez-Isaias G, Ayora-Talavera G, Bañuelos-Hernández B, Petrone-García VM, Fernández-Siurob I, Garcia-Casillas LA, Velázquez-Juárez G. as a Potential Biofactory for Antigens and Vehicle for Mucosal Application. (2023). LAPSE:2023.1793
Author Affiliations
Castellanos-Huerta I: Programa de Maestria y Doctorado en Ciencias de la Produccion y de la Salud Animal, Facultad de Medicina Veterinaria y Zootecnia, Universidad Nacional Autonoma de Mexico, Ciudad Universitaria, Ciudad de Mexico C.P. 04510, Mexico [ORCID]
Gómez-Verduzco G: Departamento de Medicina y Zootecnia de Aves, Facultad de Medicina Veterinaria y Zootecnia, Universidad Nacional Autonoma de Mexico, Avenida Universidad 3000, Ciudad de Mexico C.P. 04510, Mexico
Tellez-Isaias G: Department of Poultry Science, University of Arkansas, Fayetteville, AK 72701, USA [ORCID]
Ayora-Talavera G: Centro de Investigaciones Regionales, Dr. Hideyo Noguchi, Universidad Autonoma de Yucatán (UADY), Mérida, Yucatán C.P. 97000, Mexico [ORCID]
Bañuelos-Hernández B: Escuela de Veterinaria, Universidad De La Salle Bajío, Avenida Universidad 602, Lomas del Campestre, Leon C.P. 37150, Mexico [ORCID]
Petrone-García VM: Departamento de Ciencias Pecuarias, Facultad de Estudios Superiores Cuautitlan UNAM, Cuautitlan C.P. 54714, Mexico [ORCID]
Fernández-Siurob I: Viren SA de CV, Presidente Benito Juarez 110B, Jose Maria Arteaga, Queretaro, Queretaro C.P. 76135, Mexico
Garcia-Casillas LA: Departamento de Quimica, Centro Universitario de Ciencias Exactas e Ingenierias, Universidad de Guadalajara, Boulevard Marcelino Garcia Barragan #1421, Guadalajara, Jalisco C.P. 44430, Mexico
Velázquez-Juárez G: Departamento de Quimica, Centro Universitario de Ciencias Exactas e Ingenierias, Universidad de Guadalajara, Boulevard Marcelino Garcia Barragan #1421, Guadalajara, Jalisco C.P. 44430, Mexico [ORCID]
Gómez-Verduzco G: Departamento de Medicina y Zootecnia de Aves, Facultad de Medicina Veterinaria y Zootecnia, Universidad Nacional Autonoma de Mexico, Avenida Universidad 3000, Ciudad de Mexico C.P. 04510, Mexico
Tellez-Isaias G: Department of Poultry Science, University of Arkansas, Fayetteville, AK 72701, USA [ORCID]
Ayora-Talavera G: Centro de Investigaciones Regionales, Dr. Hideyo Noguchi, Universidad Autonoma de Yucatán (UADY), Mérida, Yucatán C.P. 97000, Mexico [ORCID]
Bañuelos-Hernández B: Escuela de Veterinaria, Universidad De La Salle Bajío, Avenida Universidad 602, Lomas del Campestre, Leon C.P. 37150, Mexico [ORCID]
Petrone-García VM: Departamento de Ciencias Pecuarias, Facultad de Estudios Superiores Cuautitlan UNAM, Cuautitlan C.P. 54714, Mexico [ORCID]
Fernández-Siurob I: Viren SA de CV, Presidente Benito Juarez 110B, Jose Maria Arteaga, Queretaro, Queretaro C.P. 76135, Mexico
Garcia-Casillas LA: Departamento de Quimica, Centro Universitario de Ciencias Exactas e Ingenierias, Universidad de Guadalajara, Boulevard Marcelino Garcia Barragan #1421, Guadalajara, Jalisco C.P. 44430, Mexico
Velázquez-Juárez G: Departamento de Quimica, Centro Universitario de Ciencias Exactas e Ingenierias, Universidad de Guadalajara, Boulevard Marcelino Garcia Barragan #1421, Guadalajara, Jalisco C.P. 44430, Mexico [ORCID]
Journal Name
Processes
Volume
10
Issue
9
First Page
1776
Year
2022
Publication Date
2022-09-04
ISSN
2227-9717
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Original Submission
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PII: pr10091776, Publication Type: Review
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LAPSE:2023.1793
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https://doi.org/10.3390/pr10091776
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