Practical Methods for Expression of Recombinant Protein in the Pichia pastoris System.

Pichia pastoris system expression practical methods recombinant protein recombinant protein expression

Journal

Current protocols
ISSN: 2691-1299
Titre abrégé: Curr Protoc
Pays: United States
ID NLM: 101773894

Informations de publication

Date de publication:
Jun 2021
Historique:
entrez: 23 6 2021
pubmed: 24 6 2021
medline: 29 6 2021
Statut: ppublish

Résumé

One of the most critical challenges of genetic engineering is the expression of recombinant proteins using biological expression systems. Nowadays, different expression systems from bacteria to mammalian tissue culture cells are available for the production of recombinant proteins for medical and industrial purposes. Among various choices, yeast expression systems such as Pichia pastoris are promising candidates. The P. pastoris expression system is a standard tool for the production of biopharmaceuticals and industrial enzymes. It is also considered a unique host for the expression of subunit vaccines which could significantly affect the growing market of medical biotechnology. Using P. pastoris as an expression system for heterologous proteins, this article provides detailed basic protocols for cloning of a recombinant cassette into a suitable expression vector, the transformation of foreign vector DNAs into the yeast by electroporation, and expression and purification of desired recombinant protein. © 2021 Wiley Periodicals LLC. Basic Protocol 1: Cloning of a recombinant cassette into a suitable expression vector Basic Protocol 2: Transformation of P. pastoris and selection of transformants Basic Protocol 3: Optimization and large-scale expression of recombinant proteins Basic Protocol 4: Purification of recombinant proteins.

Identifiants

pubmed: 34161673
doi: 10.1002/cpz1.155
doi:

Substances chimiques

Recombinant Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e155

Subventions

Organisme : Mashhad University of Medical Sciences
ID : 910071
Organisme : Mashhad University of Medical Sciences
ID : 910070
Organisme : Mashhad University of Medical Sciences
ID : 910072
Organisme : Mashhad University of Medical Sciences
ID : 910073

Informations de copyright

© 2021 Wiley Periodicals LLC.

Références

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Auteurs

Roghayeh Mohammadzadeh (R)

Department of Microbiology and Virology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.

Mohsen Karbalaei (M)

Department of Microbiology and Virology, School of Medicine, Jiroft University of Medical Sciences, Jiroft, Iran.

Saman Soleimanpour (S)

Antimicrobial Resistance Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.

Arman Mosavat (A)

Blood Borne Infections Research Center, Academic Center for Education, Culture and Research (ACECR), Razavi Khorasan, Mashhad, Iran.

Seyed Abdolrahim Rezaee (SA)

Inflammation and Inflammatory Disease Research Centre, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Immunology Research Center, Inflammation and Inflammatory Diseases Division, Mashhad University of Medical Sciences, Mashhad, Iran.

Kiarash Ghazvini (K)

Antimicrobial Resistance Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.

Hadi Farsiani (H)

Antimicrobial Resistance Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.

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