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Using directed evolution to improve hydrogen production in chimeric hydrogenases from algal species. | LitMetric

Using directed evolution to improve hydrogen production in chimeric hydrogenases from algal species.

Enzyme Microb Technol

H2OPE Biofuels LLC, Greenwood Village, CO, USA; University of West Florida, Pensacola, FL USA. Electronic address:

Published: February 2024

AI Article Synopsis

  • Algae can produce hydrogen using sunlight and water, but current methods are insufficient for industrial use.
  • Researchers created 113 gene variants of the hydrogenase enzyme by combining segments from hydrogenase genes of two algae species, aiming to improve hydrogen production.
  • The best-performing chimeras contained segments important for proton transfer, with predictions suggesting some mutants could produce 2 to 3 times more hydrogen than the wild-type enzyme.

Article Abstract

Algae generate hydrogen from sunlight and water utilizing high-energy electrons generated during photosynthesis. The amount of hydrogen produced in heterologous expression of the wild-type hydrogenase is currently insufficient for industrial applications. One approach to improve hydrogen yields is through directed evolution of the DNA of the native hydrogenase. Here, we created 113 chimeric algal hydrogenase gene variants derived from combining segments of three parent hydrogenases, two from Chlamydomonas reinhardtii (CrHydA1 and CrHydA2) and one from Scenedesmus obliquus (HydA1). To generate chimeras, there were seven segments into which each of the parent hydrogenase genes was divided and recombined in a variety of combinations. The chimeric and parental hydrogenase sequences were cloned for heterologous expression in Escherichia coli, and 40 of the resultant enzymes expressed were assayed for H production. Chimeric clones that resulted in equal or greater production obtained with the cloned CrHydA1 parent hydrogenase were those comprised of CrHydA1 sequence in segments #1, 2, 3, and/or 4. These best-performing chimeras all contained one common region, segment #2, the part of the sequence known to contain important amino acids involved in proton transfer or hydrogen cluster coordination. The amino acid sequence distances among all chimeric clones to that of the CrHydA1 parent were determined, and the relationship between sequence distances and experimentally-derived H production was evaluated. An additional model determined the correlation between electrostatic potential energy surface area ratios and H production. The model yielded several algal mutants with predicted hydrogen productions in a range of two to three times that of the wild-type hydrogenase. The mutant data and the model can now be used to predict which specific mutant sequences may result in even higher hydrogen yields. Overall, results provide more precise details in planning future directed evolution to functionally improve algal hydrogenases.

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Source
http://dx.doi.org/10.1016/j.enzmictec.2023.110349DOI Listing

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