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Cloning and expression of Aspergillus flavus urate oxidase in Pichia pastoris
Urate oxidase is an important enzyme with therapeutic and diagnostic applications. Rasburicase is a recombinant urate oxidase enzyme approved by FDA to use in the treatment of hyperuricemia conditions. Various hosts such as Saccharomyces cerevisiae, Hansenula polymorpha and Escherichia coli have bee...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4124111/ https://www.ncbi.nlm.nih.gov/pubmed/25105091 http://dx.doi.org/10.1186/2193-1801-3-395 |
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author | Fazel, Ramin Zarei, Najmeh Ghaemi, Nasser Namvaran, Mohammad Mehdi Enayati, Somayeh Mirabzadeh Ardakani, Esmat Azizi, Mohammad Khalaj, Vahid |
author_facet | Fazel, Ramin Zarei, Najmeh Ghaemi, Nasser Namvaran, Mohammad Mehdi Enayati, Somayeh Mirabzadeh Ardakani, Esmat Azizi, Mohammad Khalaj, Vahid |
author_sort | Fazel, Ramin |
collection | PubMed |
description | Urate oxidase is an important enzyme with therapeutic and diagnostic applications. Rasburicase is a recombinant urate oxidase enzyme approved by FDA to use in the treatment of hyperuricemia conditions. Various hosts such as Saccharomyces cerevisiae, Hansenula polymorpha and Escherichia coli have been used to express the enzyme. Today, Pichia pastoris is considered as an important host for heterologous protein expression since it has beneficial characteristics such as strong promoters, simple scale up, post translational modifications, high cell density cultivation and simple genetic manipulation. In this study, Aspergillus flavus urate oxidase gene was cloned in pPICZαA expression vector and expressed in P. pastoris. The recombinant urate oxidase was expressed in secretory form and was confirmed through RT-PCR, SDS-PAGE analysis and western blotting. The enzyme activity was determined using a colorimetric assay. A production yield of 0.43 U/ml of culture supernatant was obtained. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/2193-1801-3-395) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4124111 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-41241112014-08-07 Cloning and expression of Aspergillus flavus urate oxidase in Pichia pastoris Fazel, Ramin Zarei, Najmeh Ghaemi, Nasser Namvaran, Mohammad Mehdi Enayati, Somayeh Mirabzadeh Ardakani, Esmat Azizi, Mohammad Khalaj, Vahid Springerplus Research Urate oxidase is an important enzyme with therapeutic and diagnostic applications. Rasburicase is a recombinant urate oxidase enzyme approved by FDA to use in the treatment of hyperuricemia conditions. Various hosts such as Saccharomyces cerevisiae, Hansenula polymorpha and Escherichia coli have been used to express the enzyme. Today, Pichia pastoris is considered as an important host for heterologous protein expression since it has beneficial characteristics such as strong promoters, simple scale up, post translational modifications, high cell density cultivation and simple genetic manipulation. In this study, Aspergillus flavus urate oxidase gene was cloned in pPICZαA expression vector and expressed in P. pastoris. The recombinant urate oxidase was expressed in secretory form and was confirmed through RT-PCR, SDS-PAGE analysis and western blotting. The enzyme activity was determined using a colorimetric assay. A production yield of 0.43 U/ml of culture supernatant was obtained. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/2193-1801-3-395) contains supplementary material, which is available to authorized users. Springer International Publishing 2014-07-30 /pmc/articles/PMC4124111/ /pubmed/25105091 http://dx.doi.org/10.1186/2193-1801-3-395 Text en © Fazel et al.; licensee Springer. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. |
spellingShingle | Research Fazel, Ramin Zarei, Najmeh Ghaemi, Nasser Namvaran, Mohammad Mehdi Enayati, Somayeh Mirabzadeh Ardakani, Esmat Azizi, Mohammad Khalaj, Vahid Cloning and expression of Aspergillus flavus urate oxidase in Pichia pastoris |
title | Cloning and expression of Aspergillus flavus urate oxidase in Pichia pastoris |
title_full | Cloning and expression of Aspergillus flavus urate oxidase in Pichia pastoris |
title_fullStr | Cloning and expression of Aspergillus flavus urate oxidase in Pichia pastoris |
title_full_unstemmed | Cloning and expression of Aspergillus flavus urate oxidase in Pichia pastoris |
title_short | Cloning and expression of Aspergillus flavus urate oxidase in Pichia pastoris |
title_sort | cloning and expression of aspergillus flavus urate oxidase in pichia pastoris |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4124111/ https://www.ncbi.nlm.nih.gov/pubmed/25105091 http://dx.doi.org/10.1186/2193-1801-3-395 |
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