Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Shariati, Fatemeh Sadat, Keramati, Malihe, Cohan, Reza Ahangari
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
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
_version_ 1784795148221153280
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
work_keys_str_mv AT shariatifatemehsadat indirectoptimizationofstaphylokinaseexpressionlevelindicistronicautoinduciblesystem
AT keramatimalihe indirectoptimizationofstaphylokinaseexpressionlevelindicistronicautoinduciblesystem
AT cohanrezaahangari indirectoptimizationofstaphylokinaseexpressionlevelindicistronicautoinduciblesystem