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Indirect optimization of staphylokinase expression level in dicistronic auto-inducible system
Design of experiment (DOE) is a statistical approach for designing, performing, and interpreting a large set of data with the minimum number of tests. In our previous study, we developed a novel Hsp27 SILEX system for production of recombinant proteins. In the present study, we optimized indirectly...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9500143/ https://www.ncbi.nlm.nih.gov/pubmed/36138332 http://dx.doi.org/10.1186/s13568-022-01464-0 |
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author | Shariati, Fatemeh Sadat Keramati, Malihe Cohan, Reza Ahangari |
author_facet | Shariati, Fatemeh Sadat Keramati, Malihe Cohan, Reza Ahangari |
author_sort | Shariati, Fatemeh Sadat |
collection | PubMed |
description | Design of experiment (DOE) is a statistical approach for designing, performing, and interpreting a large set of data with the minimum number of tests. In our previous study, we developed a novel Hsp27 SILEX system for production of recombinant proteins. In the present study, we optimized indirectly the most effective factors including inoculation load, self-induction temperature, and culture media on autoinduction of staphylokinase (SAK) expression using RSM methodology and fluorometry. The expression level of SAK was assayed at different runs after 6 h incubation at 90 rpm. The results indicated all parameters significantly affect the SAK expression level (p < 0.05). The optimum expression condition was obtained with an inoculation load of 0.05, a temperature of 25 °C, and TB culture medium. The analysis of variance with a R(2) value of 0.91 showed that a quadratic model well described this prediction (p < 0.05). Applying the optimized condition led to an approximately fourfold increase in the SAK expression level (from 1.3 to 5.2 µg/ml). Moreover, the recombinant protein was purified using immobilized metal affinity chromatography and the activity was also confirmed by semi-quantitative caseinolytic method. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13568-022-01464-0. |
format | Online Article Text |
id | pubmed-9500143 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-95001432022-09-24 Indirect optimization of staphylokinase expression level in dicistronic auto-inducible system Shariati, Fatemeh Sadat Keramati, Malihe Cohan, Reza Ahangari AMB Express Original Article Design of experiment (DOE) is a statistical approach for designing, performing, and interpreting a large set of data with the minimum number of tests. In our previous study, we developed a novel Hsp27 SILEX system for production of recombinant proteins. In the present study, we optimized indirectly the most effective factors including inoculation load, self-induction temperature, and culture media on autoinduction of staphylokinase (SAK) expression using RSM methodology and fluorometry. The expression level of SAK was assayed at different runs after 6 h incubation at 90 rpm. The results indicated all parameters significantly affect the SAK expression level (p < 0.05). The optimum expression condition was obtained with an inoculation load of 0.05, a temperature of 25 °C, and TB culture medium. The analysis of variance with a R(2) value of 0.91 showed that a quadratic model well described this prediction (p < 0.05). Applying the optimized condition led to an approximately fourfold increase in the SAK expression level (from 1.3 to 5.2 µg/ml). Moreover, the recombinant protein was purified using immobilized metal affinity chromatography and the activity was also confirmed by semi-quantitative caseinolytic method. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13568-022-01464-0. Springer Berlin Heidelberg 2022-09-22 /pmc/articles/PMC9500143/ /pubmed/36138332 http://dx.doi.org/10.1186/s13568-022-01464-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Shariati, Fatemeh Sadat Keramati, Malihe Cohan, Reza Ahangari Indirect optimization of staphylokinase expression level in dicistronic auto-inducible system |
title | Indirect optimization of staphylokinase expression level in dicistronic auto-inducible system |
title_full | Indirect optimization of staphylokinase expression level in dicistronic auto-inducible system |
title_fullStr | Indirect optimization of staphylokinase expression level in dicistronic auto-inducible system |
title_full_unstemmed | Indirect optimization of staphylokinase expression level in dicistronic auto-inducible system |
title_short | Indirect optimization of staphylokinase expression level in dicistronic auto-inducible system |
title_sort | indirect optimization of staphylokinase expression level in dicistronic auto-inducible system |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9500143/ https://www.ncbi.nlm.nih.gov/pubmed/36138332 http://dx.doi.org/10.1186/s13568-022-01464-0 |
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