Hydrogen Production by CO2 Deprived Photoautotrophic Chlamydomonas reinhardtii Cultures

Biochemistry (Mosc). 2022 Oct;87(10):1098-1108. doi: 10.1134/S0006297922100030.

Abstract

Light-dependent hydrogen production by microalgae attracts attention of researchers because of the potential practical application. It is generally recognized that Calvin-Benson-Bassham cycle competes with hydrogen production process for electrons, and substrate (CO2) limitation of the cycle can increase hydrogen production rate. Furthermore, photosystem II is not destroyed by CO2 deficiency. We studied photoautotrophic cultures of Chlamydomonas reimhardtii under CO2 deficiency. Under the flow of air with removed CO2 the cultures reached stationary phase of growth and the photosystem II was downregulated due to overreduction of plastoquinone pool followed by degradation of the entire photosynthetic machinery. Under the Ar flow in the absence of CO2 the cultures were brought to microaerobic conditions producing small amounts of hydrogen (5 ml H2 day-1 liter-1 culture). Similar to the case of incubation under air atmosphere, prolonged incubation of cultures under microaerobic conditions resulted in down-regulation of photosystem II due to overreduction of plastoquinone pool with following degradation of whole photosynthetic machinery. Following removal of CO2, transfer of cultures into dark anaerobic conditions (2.5 h), and illumination with low-intensity light resulted in the cultures producing H2 with high initial rate. Total microalgal hydrogen production under these conditions was 56 ml H2 liter-1 culture. Thus, the CO2-deprived photoautotrophic cultures produce hydrogen. Hydrogen production was limited by the toxic effect of oxygen on hydrogenase but not by the Calvin-Benson-Bassham cycle competition with hydrogen production process.

Keywords: CO2 deprivation; Chlamydomonas reinhardtii; microalgal hydrogen production; photoautotrophic cultures.

MeSH terms

  • Carbon Dioxide / metabolism
  • Chlamydomonas reinhardtii* / metabolism
  • Hydrogen
  • Hydrogenase* / metabolism
  • Hydrogenase* / pharmacology
  • Oxygen / metabolism
  • Photosynthesis / physiology
  • Photosystem II Protein Complex / metabolism
  • Plastoquinone / pharmacology
  • Sulfur / metabolism
  • Sulfur / pharmacology

Substances

  • Photosystem II Protein Complex
  • Carbon Dioxide
  • Hydrogenase
  • Plastoquinone
  • Sulfur
  • Hydrogen
  • Oxygen