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Synthetic biology for improved hydrogen production in Chlamydomonas reinhardtii

Hydrogen is a clean alternative to fossil fuels. It has applications for electricity generation and transportation and is used for the manufacturing of ammonia and steel. However, today, H(2) is almost exclusively produced from coal and natural gas. As such, methods to produce H(2) that do not use f...

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Autores principales: King, Samuel J., Jerkovic, Ante, Brown, Louise J., Petroll, Kerstin, Willows, Robert D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9249334/
https://www.ncbi.nlm.nih.gov/pubmed/35338590
http://dx.doi.org/10.1111/1751-7915.14024
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author King, Samuel J.
Jerkovic, Ante
Brown, Louise J.
Petroll, Kerstin
Willows, Robert D.
author_facet King, Samuel J.
Jerkovic, Ante
Brown, Louise J.
Petroll, Kerstin
Willows, Robert D.
author_sort King, Samuel J.
collection PubMed
description Hydrogen is a clean alternative to fossil fuels. It has applications for electricity generation and transportation and is used for the manufacturing of ammonia and steel. However, today, H(2) is almost exclusively produced from coal and natural gas. As such, methods to produce H(2) that do not use fossil fuels need to be developed and adopted. The biological manufacturing of H(2) may be one promising solution as this process is clean and renewable. Hydrogen is produced biologically via enzymes called hydrogenases. There are three classes of hydrogenases namely [FeFe], [NiFe] and [Fe] hydrogenases. The [FeFe] hydrogenase HydA1 from the model unicellular algae Chlamydomonas reinhardtii has been studied extensively and belongs to the A1 subclass of [FeFe] hydrogenases that have the highest turnover frequencies amongst hydrogenases (21,000 ± 12,000 H(2) s(−1) for CaHydA from Clostridium acetobutyliticum). Yet to date, limitations in C. reinhardtii H(2) production pathways have hampered commercial scale implementation, in part due to O(2) sensitivity of hydrogenases and competing metabolic pathways, resulting in low H(2) production efficiency. Here, we describe key processes in the biogenesis of HydA1 and H(2) production pathways in C. reinhardtii. We also summarize recent advancements of algal H(2) production using synthetic biology and describe valuable tools such as high‐throughput screening (HTS) assays to accelerate the process of engineering algae for commercial biological H(2) production.
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spelling pubmed-92493342022-07-05 Synthetic biology for improved hydrogen production in Chlamydomonas reinhardtii King, Samuel J. Jerkovic, Ante Brown, Louise J. Petroll, Kerstin Willows, Robert D. Microb Biotechnol Minireviews Hydrogen is a clean alternative to fossil fuels. It has applications for electricity generation and transportation and is used for the manufacturing of ammonia and steel. However, today, H(2) is almost exclusively produced from coal and natural gas. As such, methods to produce H(2) that do not use fossil fuels need to be developed and adopted. The biological manufacturing of H(2) may be one promising solution as this process is clean and renewable. Hydrogen is produced biologically via enzymes called hydrogenases. There are three classes of hydrogenases namely [FeFe], [NiFe] and [Fe] hydrogenases. The [FeFe] hydrogenase HydA1 from the model unicellular algae Chlamydomonas reinhardtii has been studied extensively and belongs to the A1 subclass of [FeFe] hydrogenases that have the highest turnover frequencies amongst hydrogenases (21,000 ± 12,000 H(2) s(−1) for CaHydA from Clostridium acetobutyliticum). Yet to date, limitations in C. reinhardtii H(2) production pathways have hampered commercial scale implementation, in part due to O(2) sensitivity of hydrogenases and competing metabolic pathways, resulting in low H(2) production efficiency. Here, we describe key processes in the biogenesis of HydA1 and H(2) production pathways in C. reinhardtii. We also summarize recent advancements of algal H(2) production using synthetic biology and describe valuable tools such as high‐throughput screening (HTS) assays to accelerate the process of engineering algae for commercial biological H(2) production. John Wiley and Sons Inc. 2022-03-26 /pmc/articles/PMC9249334/ /pubmed/35338590 http://dx.doi.org/10.1111/1751-7915.14024 Text en © 2022 The Authors. Microbial Biotechnology published by Society for Applied Microbiology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Minireviews
King, Samuel J.
Jerkovic, Ante
Brown, Louise J.
Petroll, Kerstin
Willows, Robert D.
Synthetic biology for improved hydrogen production in Chlamydomonas reinhardtii
title Synthetic biology for improved hydrogen production in Chlamydomonas reinhardtii
title_full Synthetic biology for improved hydrogen production in Chlamydomonas reinhardtii
title_fullStr Synthetic biology for improved hydrogen production in Chlamydomonas reinhardtii
title_full_unstemmed Synthetic biology for improved hydrogen production in Chlamydomonas reinhardtii
title_short Synthetic biology for improved hydrogen production in Chlamydomonas reinhardtii
title_sort synthetic biology for improved hydrogen production in chlamydomonas reinhardtii
topic Minireviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9249334/
https://www.ncbi.nlm.nih.gov/pubmed/35338590
http://dx.doi.org/10.1111/1751-7915.14024
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