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Reducing conditions are the key for efficient production of active ribonuclease inhibitor in Escherichia coli

BACKGROUND: The eukaryotic RNase ribonuclease/angiogenin inhibitors (RI) are a protein group distinguished by a unique structure - they are composed of hydrophobic leucine-rich repeat motifs (LRR) and contain a high amount of reduced cysteine residues. The members of this group are difficult to prod...

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Autores principales: Šiurkus, Juozas, Neubauer, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3112386/
https://www.ncbi.nlm.nih.gov/pubmed/21554746
http://dx.doi.org/10.1186/1475-2859-10-31
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author Šiurkus, Juozas
Neubauer, Peter
author_facet Šiurkus, Juozas
Neubauer, Peter
author_sort Šiurkus, Juozas
collection PubMed
description BACKGROUND: The eukaryotic RNase ribonuclease/angiogenin inhibitors (RI) are a protein group distinguished by a unique structure - they are composed of hydrophobic leucine-rich repeat motifs (LRR) and contain a high amount of reduced cysteine residues. The members of this group are difficult to produce in E. coli and other recombinant hosts due to their high aggregation tendency. RESULTS: In this work dithiothreitol (DTT) was successfully applied for improving the yield of correctly folded ribonuclease/angiogenin inhibitor in E. coli K12 periplasmic and cytoplasmic compartments. The feasibility of the in vivo folding concepts for cytoplasmic and periplasmic production were demonstrated at batch and fed-batch cultivation modes in shake flasks and at the bioreactor scale. Firstly, the best secretion conditions of RI in the periplasmic space were evaluated by using a high throughput multifactorial screening approach of a vector library, directly with the Enbase fed-batch production mode in 96-well plates. Secondly, the effect of the redox environment was evaluated in isogenic dsbA(+ )and dsbA(- )strains at the various cultivation conditions with reducing agents in the cultivation medium. Despite the fusion to the signal peptide, highest activities were found in the cytoplasmic fraction. Thus by removing the signal peptide the positive effect of the reducing agent DTT was clearly proven also for the cytoplasmic compartment. Finally, optimal periplasmic and cytoplasmic RI fed-batch production processes involving externally added DTT were developed in shake flasks and scaled up to the bioreactor scale. CONCLUSIONS: DTT highly improved both, periplasmic and cytoplasmic accumulation and activity of RI at low synthesis rate, i.e. in constructs harbouring weak recombinant synthesis rate stipulating genetic elements together with cultivation at low temperature. In a stirred bioreactor environment RI folding was strongly improved by repeated pulse addition of DTT at low aeration conditions.
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spelling pubmed-31123862011-06-12 Reducing conditions are the key for efficient production of active ribonuclease inhibitor in Escherichia coli Šiurkus, Juozas Neubauer, Peter Microb Cell Fact Research BACKGROUND: The eukaryotic RNase ribonuclease/angiogenin inhibitors (RI) are a protein group distinguished by a unique structure - they are composed of hydrophobic leucine-rich repeat motifs (LRR) and contain a high amount of reduced cysteine residues. The members of this group are difficult to produce in E. coli and other recombinant hosts due to their high aggregation tendency. RESULTS: In this work dithiothreitol (DTT) was successfully applied for improving the yield of correctly folded ribonuclease/angiogenin inhibitor in E. coli K12 periplasmic and cytoplasmic compartments. The feasibility of the in vivo folding concepts for cytoplasmic and periplasmic production were demonstrated at batch and fed-batch cultivation modes in shake flasks and at the bioreactor scale. Firstly, the best secretion conditions of RI in the periplasmic space were evaluated by using a high throughput multifactorial screening approach of a vector library, directly with the Enbase fed-batch production mode in 96-well plates. Secondly, the effect of the redox environment was evaluated in isogenic dsbA(+ )and dsbA(- )strains at the various cultivation conditions with reducing agents in the cultivation medium. Despite the fusion to the signal peptide, highest activities were found in the cytoplasmic fraction. Thus by removing the signal peptide the positive effect of the reducing agent DTT was clearly proven also for the cytoplasmic compartment. Finally, optimal periplasmic and cytoplasmic RI fed-batch production processes involving externally added DTT were developed in shake flasks and scaled up to the bioreactor scale. CONCLUSIONS: DTT highly improved both, periplasmic and cytoplasmic accumulation and activity of RI at low synthesis rate, i.e. in constructs harbouring weak recombinant synthesis rate stipulating genetic elements together with cultivation at low temperature. In a stirred bioreactor environment RI folding was strongly improved by repeated pulse addition of DTT at low aeration conditions. BioMed Central 2011-05-10 /pmc/articles/PMC3112386/ /pubmed/21554746 http://dx.doi.org/10.1186/1475-2859-10-31 Text en Copyright ©2011 Šiurkus and Neubauer; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Šiurkus, Juozas
Neubauer, Peter
Reducing conditions are the key for efficient production of active ribonuclease inhibitor in Escherichia coli
title Reducing conditions are the key for efficient production of active ribonuclease inhibitor in Escherichia coli
title_full Reducing conditions are the key for efficient production of active ribonuclease inhibitor in Escherichia coli
title_fullStr Reducing conditions are the key for efficient production of active ribonuclease inhibitor in Escherichia coli
title_full_unstemmed Reducing conditions are the key for efficient production of active ribonuclease inhibitor in Escherichia coli
title_short Reducing conditions are the key for efficient production of active ribonuclease inhibitor in Escherichia coli
title_sort reducing conditions are the key for efficient production of active ribonuclease inhibitor in escherichia coli
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3112386/
https://www.ncbi.nlm.nih.gov/pubmed/21554746
http://dx.doi.org/10.1186/1475-2859-10-31
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