Recombinant protein production is a multibillion-dollar market. The development of a new product begins with the choice of a production host. While one single perfect host for every protein does not exist, several expression systems ranging from bacterial hosts to mammalian cells have been established. Among them, yeast cell factories combine the advantages of being single cells, such as fast growth and easy genetic manipulation, as well as eukaryotic features including a secretory pathway leading to correct protein processing and post-translational modifications. In this respect, especially the engineering of yeast glycosylation to produce glycoproteins of human-like glycan structures is of great interest. Additionally, different attempts of cellular engineering as well as the design of different production processes that are leading to improved productivities are presented. With the advent of cheaper next-generation sequencing techniques, systems biotechnology approaches focusing on genome scale analyses will advance and accelerate yeast cell factories and thus recombinant protein production processes in the near future. In this review we summarize advantages and limitations of the main and most promising yeast hosts, including Saccharomyces cerevisiae, Pichia pastoris, and Hansenula polymorpha as those presently used in large scale production of heterologous proteins.

Mattanovich, D., Branduardi, P., Dato, L., Gasser, B., Sauer, M., Porro, D. (2012). Recombinant protein production in yeasts. In A. Lorence (a cura di), Recombinant Gene Expression: Reviews And Protocols, Third Edition (pp. 329-358). Totowa, NJ : Humana Press [10.1007/978-1-61779-433-9_17].

Recombinant protein production in yeasts

BRANDUARDI, PAOLA;DATO, LAURA;PORRO, DANILO
2012

Abstract

Recombinant protein production is a multibillion-dollar market. The development of a new product begins with the choice of a production host. While one single perfect host for every protein does not exist, several expression systems ranging from bacterial hosts to mammalian cells have been established. Among them, yeast cell factories combine the advantages of being single cells, such as fast growth and easy genetic manipulation, as well as eukaryotic features including a secretory pathway leading to correct protein processing and post-translational modifications. In this respect, especially the engineering of yeast glycosylation to produce glycoproteins of human-like glycan structures is of great interest. Additionally, different attempts of cellular engineering as well as the design of different production processes that are leading to improved productivities are presented. With the advent of cheaper next-generation sequencing techniques, systems biotechnology approaches focusing on genome scale analyses will advance and accelerate yeast cell factories and thus recombinant protein production processes in the near future. In this review we summarize advantages and limitations of the main and most promising yeast hosts, including Saccharomyces cerevisiae, Pichia pastoris, and Hansenula polymorpha as those presently used in large scale production of heterologous proteins.
Capitolo o saggio
Gene Expression Regulation, Fungal; Promoter Regions, Genetic; Recombinant Proteins; Transformation, Genetic; Genetic Vectors; Cytoplasm; Pichia; Systems Biology; Glycosylation; Models, Biological; Biotechnology; Saccharomyces cerevisiae
English
Recombinant Gene Expression: Reviews And Protocols, Third Edition
Lorence, A
2012
978-161779432-2
824
Humana Press
329
358
Mattanovich, D., Branduardi, P., Dato, L., Gasser, B., Sauer, M., Porro, D. (2012). Recombinant protein production in yeasts. In A. Lorence (a cura di), Recombinant Gene Expression: Reviews And Protocols, Third Edition (pp. 329-358). Totowa, NJ : Humana Press [10.1007/978-1-61779-433-9_17].
none
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/34306
Citazioni
  • Scopus 252
  • ???jsp.display-item.citation.isi??? 218
Social impact