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The effect of non-thermal atmospheric plasma on the production and activity of recombinant phytase enzyme

Atmospheric pressure cold plasma (ACP) is introduced as a useful tool in a variety of biological applications. Proteins are the most abundant macromolecules in living systems with a central role in all biological processes. These organic molecules are modified by ACP exposure that is responsible for...

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Autores principales: Farasat, Mahsa, Arjmand, Sareh, Ranaei Siadat, Seyed Omid, Sefidbakht, Yahya, Ghomi, Hamid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6226467/
https://www.ncbi.nlm.nih.gov/pubmed/30413721
http://dx.doi.org/10.1038/s41598-018-34239-4
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author Farasat, Mahsa
Arjmand, Sareh
Ranaei Siadat, Seyed Omid
Sefidbakht, Yahya
Ghomi, Hamid
author_facet Farasat, Mahsa
Arjmand, Sareh
Ranaei Siadat, Seyed Omid
Sefidbakht, Yahya
Ghomi, Hamid
author_sort Farasat, Mahsa
collection PubMed
description Atmospheric pressure cold plasma (ACP) is introduced as a useful tool in a variety of biological applications. Proteins are the most abundant macromolecules in living systems with a central role in all biological processes. These organic molecules are modified by ACP exposure that is responsible for many of ACP’s biological effects. This study evaluated the effect of ACP on the production of recombinant phytase in yeast Pichia pastoris (P. pastoris) as well as the structure and function of the phytase enzyme. The results indicated that yeast cells treated with ACP, directly or indirectly, produced higher amounts of recombinant phytase, which was associated with the time of ACP treatment. The exposure of commercial phytase solution with ACP caused a significant increase in the enzyme activity (125%) after 4 hours. Evaluation of the phytase solution by far- and near-UV circular dichroism (CD) and fluorescence analysis indicated that this protein maintained its secondary structure when exposed to ACP while the tertiary structure was slightly unfolded. The effects of heat and H(2)O(2) on the phytase structure and function were compared with the effect of ACP treatment. The modification of Cys, Tyr and Trp amino acids upon reactive oxygen/nitrogen spices was simulated using a molecular dynamics approach. RMSF and RMSD analysis suggested that this structural alteration occurs owing to changes made by reactive species in accessible amino acids.
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spelling pubmed-62264672018-11-13 The effect of non-thermal atmospheric plasma on the production and activity of recombinant phytase enzyme Farasat, Mahsa Arjmand, Sareh Ranaei Siadat, Seyed Omid Sefidbakht, Yahya Ghomi, Hamid Sci Rep Article Atmospheric pressure cold plasma (ACP) is introduced as a useful tool in a variety of biological applications. Proteins are the most abundant macromolecules in living systems with a central role in all biological processes. These organic molecules are modified by ACP exposure that is responsible for many of ACP’s biological effects. This study evaluated the effect of ACP on the production of recombinant phytase in yeast Pichia pastoris (P. pastoris) as well as the structure and function of the phytase enzyme. The results indicated that yeast cells treated with ACP, directly or indirectly, produced higher amounts of recombinant phytase, which was associated with the time of ACP treatment. The exposure of commercial phytase solution with ACP caused a significant increase in the enzyme activity (125%) after 4 hours. Evaluation of the phytase solution by far- and near-UV circular dichroism (CD) and fluorescence analysis indicated that this protein maintained its secondary structure when exposed to ACP while the tertiary structure was slightly unfolded. The effects of heat and H(2)O(2) on the phytase structure and function were compared with the effect of ACP treatment. The modification of Cys, Tyr and Trp amino acids upon reactive oxygen/nitrogen spices was simulated using a molecular dynamics approach. RMSF and RMSD analysis suggested that this structural alteration occurs owing to changes made by reactive species in accessible amino acids. Nature Publishing Group UK 2018-11-09 /pmc/articles/PMC6226467/ /pubmed/30413721 http://dx.doi.org/10.1038/s41598-018-34239-4 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Farasat, Mahsa
Arjmand, Sareh
Ranaei Siadat, Seyed Omid
Sefidbakht, Yahya
Ghomi, Hamid
The effect of non-thermal atmospheric plasma on the production and activity of recombinant phytase enzyme
title The effect of non-thermal atmospheric plasma on the production and activity of recombinant phytase enzyme
title_full The effect of non-thermal atmospheric plasma on the production and activity of recombinant phytase enzyme
title_fullStr The effect of non-thermal atmospheric plasma on the production and activity of recombinant phytase enzyme
title_full_unstemmed The effect of non-thermal atmospheric plasma on the production and activity of recombinant phytase enzyme
title_short The effect of non-thermal atmospheric plasma on the production and activity of recombinant phytase enzyme
title_sort effect of non-thermal atmospheric plasma on the production and activity of recombinant phytase enzyme
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6226467/
https://www.ncbi.nlm.nih.gov/pubmed/30413721
http://dx.doi.org/10.1038/s41598-018-34239-4
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