Cargando…

Influence of pH control in the formation of inclusion bodies during production of recombinant sphingomyelinase-D in Escherichia coli

BACKGROUND: Inclusion bodies (IBs) are aggregated proteins that form clusters when protein is overexpressed in heterologous expression systems. IBs have been considered as non-usable proteins, but recently they are being used as functional materials, catalytic particles, drug delivery agents, immuno...

Descripción completa

Detalles Bibliográficos
Autores principales: Castellanos-Mendoza, Andrea, Castro-Acosta, Ricardo M, Olvera, Alejandro, Zavala, Guadalupe, Mendoza-Vera, Miguel, García-Hernández, Enrique, Alagón, Alejandro, Trujillo-Roldán, Mauricio A, Valdez-Cruz, Norma A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4177172/
https://www.ncbi.nlm.nih.gov/pubmed/25213001
http://dx.doi.org/10.1186/s12934-014-0137-9
_version_ 1782336734869061632
author Castellanos-Mendoza, Andrea
Castro-Acosta, Ricardo M
Olvera, Alejandro
Zavala, Guadalupe
Mendoza-Vera, Miguel
García-Hernández, Enrique
Alagón, Alejandro
Trujillo-Roldán, Mauricio A
Valdez-Cruz, Norma A
author_facet Castellanos-Mendoza, Andrea
Castro-Acosta, Ricardo M
Olvera, Alejandro
Zavala, Guadalupe
Mendoza-Vera, Miguel
García-Hernández, Enrique
Alagón, Alejandro
Trujillo-Roldán, Mauricio A
Valdez-Cruz, Norma A
author_sort Castellanos-Mendoza, Andrea
collection PubMed
description BACKGROUND: Inclusion bodies (IBs) are aggregated proteins that form clusters when protein is overexpressed in heterologous expression systems. IBs have been considered as non-usable proteins, but recently they are being used as functional materials, catalytic particles, drug delivery agents, immunogenic structures, and as a raw material in recombinant therapeutic protein purification. However, few studies have been made to understand how culture conditions affect the protein aggregation and the physicochemical characteristics that lead them to cluster. The objective of our research was to understand how pH affects the physicochemical properties of IBs formed by the recombinant sphingomyelinase-D of tick expressed in E. coli BL21-Gold (DE3) by evaluating two pH culture strategies. RESULTS: Uncontrolled pH culture conditions favored recombinant sphingomyelinase-D aggregation and IB formation. The IBs of sphingomyelinase-D produced under controlled pH at 7.5 and after 24 h were smaller (<500 nm) than those produced under uncontrolled pH conditions (>500 nm). Furthermore, the composition, conformation and β-structure formation of the aggregates were different. Under controlled pH conditions in comparison to uncontrolled conditions, the produced IBs presented higher resistance to denaturants and proteinase-K degradation, presented β-structure, but apparently as time passes the IBs become compacted and less sensitive to amyloid dye binding. CONCLUSIONS: The manipulation of the pH has an impact on IB formation and their physicochemical characteristics. Particularly, uncontrolled pH conditions favored the protein aggregation and sphingomyelinase-D IB formation. The evidence may lead to find methodologies for bioprocesses to obtain biomaterials with particular characteristics, extending the application possibilities of the inclusion bodies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-014-0137-9) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4177172
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-41771722014-09-28 Influence of pH control in the formation of inclusion bodies during production of recombinant sphingomyelinase-D in Escherichia coli Castellanos-Mendoza, Andrea Castro-Acosta, Ricardo M Olvera, Alejandro Zavala, Guadalupe Mendoza-Vera, Miguel García-Hernández, Enrique Alagón, Alejandro Trujillo-Roldán, Mauricio A Valdez-Cruz, Norma A Microb Cell Fact Research BACKGROUND: Inclusion bodies (IBs) are aggregated proteins that form clusters when protein is overexpressed in heterologous expression systems. IBs have been considered as non-usable proteins, but recently they are being used as functional materials, catalytic particles, drug delivery agents, immunogenic structures, and as a raw material in recombinant therapeutic protein purification. However, few studies have been made to understand how culture conditions affect the protein aggregation and the physicochemical characteristics that lead them to cluster. The objective of our research was to understand how pH affects the physicochemical properties of IBs formed by the recombinant sphingomyelinase-D of tick expressed in E. coli BL21-Gold (DE3) by evaluating two pH culture strategies. RESULTS: Uncontrolled pH culture conditions favored recombinant sphingomyelinase-D aggregation and IB formation. The IBs of sphingomyelinase-D produced under controlled pH at 7.5 and after 24 h were smaller (<500 nm) than those produced under uncontrolled pH conditions (>500 nm). Furthermore, the composition, conformation and β-structure formation of the aggregates were different. Under controlled pH conditions in comparison to uncontrolled conditions, the produced IBs presented higher resistance to denaturants and proteinase-K degradation, presented β-structure, but apparently as time passes the IBs become compacted and less sensitive to amyloid dye binding. CONCLUSIONS: The manipulation of the pH has an impact on IB formation and their physicochemical characteristics. Particularly, uncontrolled pH conditions favored the protein aggregation and sphingomyelinase-D IB formation. The evidence may lead to find methodologies for bioprocesses to obtain biomaterials with particular characteristics, extending the application possibilities of the inclusion bodies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-014-0137-9) contains supplementary material, which is available to authorized users. BioMed Central 2014-09-12 /pmc/articles/PMC4177172/ /pubmed/25213001 http://dx.doi.org/10.1186/s12934-014-0137-9 Text en © Castellanos-Mendoza et al.; licensee BioMed Central Ltd. 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Castellanos-Mendoza, Andrea
Castro-Acosta, Ricardo M
Olvera, Alejandro
Zavala, Guadalupe
Mendoza-Vera, Miguel
García-Hernández, Enrique
Alagón, Alejandro
Trujillo-Roldán, Mauricio A
Valdez-Cruz, Norma A
Influence of pH control in the formation of inclusion bodies during production of recombinant sphingomyelinase-D in Escherichia coli
title Influence of pH control in the formation of inclusion bodies during production of recombinant sphingomyelinase-D in Escherichia coli
title_full Influence of pH control in the formation of inclusion bodies during production of recombinant sphingomyelinase-D in Escherichia coli
title_fullStr Influence of pH control in the formation of inclusion bodies during production of recombinant sphingomyelinase-D in Escherichia coli
title_full_unstemmed Influence of pH control in the formation of inclusion bodies during production of recombinant sphingomyelinase-D in Escherichia coli
title_short Influence of pH control in the formation of inclusion bodies during production of recombinant sphingomyelinase-D in Escherichia coli
title_sort influence of ph control in the formation of inclusion bodies during production of recombinant sphingomyelinase-d in escherichia coli
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4177172/
https://www.ncbi.nlm.nih.gov/pubmed/25213001
http://dx.doi.org/10.1186/s12934-014-0137-9
work_keys_str_mv AT castellanosmendozaandrea influenceofphcontrolintheformationofinclusionbodiesduringproductionofrecombinantsphingomyelinasedinescherichiacoli
AT castroacostaricardom influenceofphcontrolintheformationofinclusionbodiesduringproductionofrecombinantsphingomyelinasedinescherichiacoli
AT olveraalejandro influenceofphcontrolintheformationofinclusionbodiesduringproductionofrecombinantsphingomyelinasedinescherichiacoli
AT zavalaguadalupe influenceofphcontrolintheformationofinclusionbodiesduringproductionofrecombinantsphingomyelinasedinescherichiacoli
AT mendozaveramiguel influenceofphcontrolintheformationofinclusionbodiesduringproductionofrecombinantsphingomyelinasedinescherichiacoli
AT garciahernandezenrique influenceofphcontrolintheformationofinclusionbodiesduringproductionofrecombinantsphingomyelinasedinescherichiacoli
AT alagonalejandro influenceofphcontrolintheformationofinclusionbodiesduringproductionofrecombinantsphingomyelinasedinescherichiacoli
AT trujilloroldanmauricioa influenceofphcontrolintheformationofinclusionbodiesduringproductionofrecombinantsphingomyelinasedinescherichiacoli
AT valdezcruznormaa influenceofphcontrolintheformationofinclusionbodiesduringproductionofrecombinantsphingomyelinasedinescherichiacoli