5′-untranslated region sequences enhance plasmid-based protein production in Sulfolobus acidocaldarius

<i>Sulfolobus acidocaldarius</i>, a thermoacidophilic archaeon of the phylum Thermoproteota (former Crenarchaeota), is a widely used model organism for gene deletion studies and recombinant protein production. Previous research has demonstrated the efficacy of the <i>saci_2122</i> promoter (P<sub>ara</sub>), providing low basal activity and high pentose-dependent induction. However, the available expression vector does not include a 5'-terminal untranslated region (5'-UTR), a typical element found in bacterial expression vectors that usually enhances protein production in bacteria. To establish <i>S. acidocaldarius</i> as a production strain in biotechnology in the long term, it is intrinsically relevant to optimize its tools and capacities to increase production efficiencies. Here we show that protein production is increased by the integration of <i>S. acidocaldarius</i> 5'-UTRs into P<sub>ara</sub> expression plasmids. Using the esterase Saci_1116 as a reporter protein, we observed a four-fold increase in soluble and active protein yield upon insertion of the <i>saci_1322</i> (<i>alba</i>) 5'-UTR. Screening of four additional 5'-UTRs from other highly abundant proteins (<i>thα</i>, <i>slaA</i>, <i>slaB, saci_0330</i>) revealed a consistent enhancement in target protein production. Additionally, site-directed mutagenesis of the Shine-Dalgarno (SD) motif within the <i>alba</i> 5'-UTR revealed its significance for protein synthesis. Ultimately, the <i>alba</i> 5'-UTR optimized expression vector improved the expression of various proteins, including six glycosyltransferases and one hydroxyacyl-CoA dehydratase from <i>S. acidocaldarius</i>, and a malto-oligosyltrehalose trehalohydrolase from <i>Saccharolobus solfataricus</i>, demonstrating its applicability. Our results show that the integration of SD-motif containing 5'-UTRs significantly enhanced plasmid-based protein production in <i>S. acidocaldarius</i>. This advancement in recombinant expression not only broadens the utility of <i>S. acidocaldarius</i> as an archaeal expression platform but also marks an important step toward potential biotechnological applications.

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Publication Details

Journal
Frontiers in Microbiology
Published
2024-11-25
DOI
https://doi.org/10.3389/fmicb.2024.1443342
Citations
5
Primary Topic
Enzyme Production and Characterization
Type
article
Field-Weighted Citation Impact
1.93

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article

5′-untranslated region sequences enhance plasmid-based protein production in Sulfolobus acidocaldarius

Christian Schmerling, Bettina Siebers, Jörn Kalinowski, Christopher Bräsen et al.
5 citations
Frontiers in Microbiology
Enzyme Production and Characterization
1.93
article

5′-untranslated region sequences enhance plasmid-based protein production in Sulfolobus acidocaldarius

Christian Schmerling, Bettina Siebers, Jörn Kalinowski, Christopher Bräsen, Tobias Busche, Laura Kuschmierz, Alexander Wagner
article en
5 citations

Abstract

<i>Sulfolobus acidocaldarius</i>, a thermoacidophilic archaeon of the phylum Thermoproteota (former Crenarchaeota), is a widely used model organism for gene deletion studies and recombinant protein production. Previous research has demonstrated the efficacy of the <i>saci_2122</i> promoter (P<sub>ara</sub>), providing low basal activity and high pentose-dependent induction. However, the available expression vector does not include a 5'-terminal untranslated region (5'-UTR), a typical element found in bacterial expression vectors that usually enhances protein production in bacteria. To establish <i>S. acidocaldarius</i> as a production strain in biotechnology in the long term, it is intrinsically relevant to optimize its tools and capacities to increase production efficiencies. Here we show that protein production is increased by the integration of <i>S. acidocaldarius</i> 5'-UTRs into P<sub>ara</sub> expression plasmids. Using the esterase Saci_1116 as a reporter protein, we observed a four-fold increase in soluble and active protein yield upon insertion of the <i>saci_1322</i> (<i>alba</i>) 5'-UTR. Screening of four additional 5'-UTRs from other highly abundant proteins (<i>thα</i>, <i>slaA</i>, <i>slaB, saci_0330</i>) revealed a consistent enhancement in target protein production. Additionally, site-directed mutagenesis of the Shine-Dalgarno (SD) motif within the <i>alba</i> 5'-UTR revealed its significance for protein synthesis. Ultimately, the <i>alba</i> 5'-UTR optimized expression vector improved the expression of various proteins, including six glycosyltransferases and one hydroxyacyl-CoA dehydratase from <i>S. acidocaldarius</i>, and a malto-oligosyltrehalose trehalohydrolase from <i>Saccharolobus solfataricus</i>, demonstrating its applicability. Our results show that the integration of SD-motif containing 5'-UTRs significantly enhanced plasmid-based protein production in <i>S. acidocaldarius</i>. This advancement in recombinant expression not only broadens the utility of <i>S. acidocaldarius</i> as an archaeal expression platform but also marks an important step toward potential biotechnological applications.

Frontiers in MicrobiologyVol. 15
Bielefeld University (DE), University of Duisburg-Essen (DE)
Universität Duisburg-Essen
Openalex Percentile: Top 15%
Enzyme Production and Characterization
1.93
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