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      Implementation of a high cell density fed-batch for heterologous production of active [NiFe]-hydrogenase in Escherichia coli bioreactor cultivations

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          Abstract

          Background

          O 2-tolerant [NiFe]-hydrogenases offer tremendous potential for applications in H 2-based technology. As these metalloenzymes undergo a complicated maturation process that requires a dedicated set of multiple accessory proteins, their heterologous production is challenging, thus hindering their fundamental understanding and the development of related applications. Taking these challenges into account, we selected the comparably simple regulatory [NiFe]-hydrogenase (RH) from Cupriavidus necator as a model for the development of bioprocesses for heterologous [NiFe]-hydrogenase production. We already reported recently on the high-yield production of catalytically active RH in Escherichia coli by optimizing the culture conditions in shake flasks.

          Results

          In this study, we further increase the RH yield and ensure consistent product quality by a rationally designed high cell density fed-batch cultivation process. Overall, the bioreactor cultivations resulted in ˃130 mg L −1 of catalytically active RH which is a more than 100-fold increase compared to other RH laboratory bioreactor scale processes with C. necator. Furthermore, the process shows high reproducibility of the previously selected optimized conditions and high productivity.

          Conclusions

          This work provides a good opportunity to readily supply such difficult-to-express complex metalloproteins economically and at high concentrations to meet the demand in basic and applied studies.

          Supplementary Information

          The online version contains supplementary material available at 10.1186/s12934-022-01919-w.

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          Most cited references63

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          Hydrogenases.

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            Enzymes as working or inspirational electrocatalysts for fuel cells and electrolysis.

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              Genomic and metagenomic surveys of hydrogenase distribution indicate H2 is a widely utilised energy source for microbial growth and survival.

              Recent physiological and ecological studies have challenged the long-held belief that microbial metabolism of molecular hydrogen (H2) is a niche process. To gain a broader insight into the importance of microbial H2 metabolism, we comprehensively surveyed the genomic and metagenomic distribution of hydrogenases, the reversible enzymes that catalyse the oxidation and evolution of H2. The protein sequences of 3286 non-redundant putative hydrogenases were curated from publicly available databases. These metalloenzymes were classified into multiple groups based on (1) amino acid sequence phylogeny, (2) metal-binding motifs, (3) predicted genetic organisation and (4) reported biochemical characteristics. Four groups (22 subgroups) of [NiFe]-hydrogenase, three groups (6 subtypes) of [FeFe]-hydrogenases and a small group of [Fe]-hydrogenases were identified. We predict that this hydrogenase diversity supports H2-based respiration, fermentation and carbon fixation processes in both oxic and anoxic environments, in addition to various H2-sensing, electron-bifurcation and energy-conversion mechanisms. Hydrogenase-encoding genes were identified in 51 bacterial and archaeal phyla, suggesting strong pressure for both vertical and lateral acquisition. Furthermore, hydrogenase genes could be recovered from diverse terrestrial, aquatic and host-associated metagenomes in varying proportions, indicating a broad ecological distribution and utilisation. Oxygen content (pO2) appears to be a central factor driving the phylum- and ecosystem-level distribution of these genes. In addition to compounding evidence that H2 was the first electron donor for life, our analysis suggests that the great diversification of hydrogenases has enabled H2 metabolism to sustain the growth or survival of microorganisms in a wide range of ecosystems to the present day. This work also provides a comprehensive expanded system for classifying hydrogenases and identifies new prospects for investigating H2 metabolism.
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                Author and article information

                Contributors
                qin.fan@campus.tu-berlin.de
                saskia.waldburger@campus.tu-berlin.de
                peter.neubauer@tu-berlin.de
                riedel@tu-berlin.de
                matthias.gimpel@tu-berlin.de
                Journal
                Microb Cell Fact
                Microb Cell Fact
                Microbial Cell Factories
                BioMed Central (London )
                1475-2859
                19 September 2022
                19 September 2022
                2022
                : 21
                : 193
                Affiliations
                GRID grid.6734.6, ISNI 0000 0001 2292 8254, Chair of Bioprocess Engineering, , Technische Universität Berlin, ; Ackerstr. 76, ACK24, D-13355 Berlin, Germany
                Author information
                http://orcid.org/0000-0001-5801-8690
                http://orcid.org/0000-0001-7008-1609
                http://orcid.org/0000-0002-1214-9713
                http://orcid.org/0000-0003-1373-417X
                http://orcid.org/0000-0002-5136-8169
                Article
                1919
                10.1186/s12934-022-01919-w
                9484157
                36123684
                8455ef23-a67e-431f-859d-08977d8b9ab6
                © The Author(s) 2022

                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/. 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 in a credit line to the data.

                History
                : 27 July 2022
                : 7 September 2022
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100001659, Deutsche Forschungsgemeinschaft;
                Award ID: EXC 2008/1-390540038
                Award ID: EXC 2008/1-390540038
                Award ID: EXC 2008/1-390540038
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100001655, Deutscher Akademischer Austauschdienst;
                Funded by: Technische Universität Berlin (3136)
                Categories
                Research
                Custom metadata
                © The Author(s) 2022

                Biotechnology
                metalloprotein,regulatory hydrogenase,high cell density fed-batch,escherichia coli,[nife]-hydrogenase

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