In-vivo turnover frequency of the cyanobacterial NiFe-hydrogenase during photohydrogen production outperforms in-vitro systems

Sci Rep. 2018 Apr 17;8(1):6083. doi: 10.1038/s41598-018-24430-y.

Abstract

Cyanobacteria provide all components for sunlight driven biohydrogen production. Their bidirectional NiFe-hydrogenase is resistant against low levels of oxygen with a preference for hydrogen evolution. However, until now it was unclear if its catalytic efficiency can keep pace with the photosynthetic electron transfer rate. We identified NikKLMQO (sll0381-sll0385) as a nickel transporter, which is required for hydrogen production. ICP-MS measurements were used to quantify hydrogenase molecules per cell. We found 400 to 2000 hydrogenase molecules per cell depending on the conditions. In-vivo turnover frequencies of the enzyme ranged from 62 H2/s in the wild type to 120 H2/s in a mutant during photohydrogen production. These frequencies are above maximum in-vivo photosynthetic electron transfer rates of 47 e-/s (equivalent to 24 H2/s). They are also above those of existing in-vitro systems working with unlimited electron supply and show that in-vivo photohydrogen production is limited by electron delivery to the enzyme.

MeSH terms

  • Bacterial Proteins / metabolism*
  • Electron Transport
  • Hydrogen / metabolism*
  • Hydrogenase / metabolism*
  • Nickel / metabolism
  • Photosynthesis
  • Synechocystis / metabolism*
  • Urease / metabolism

Substances

  • Bacterial Proteins
  • Nickel
  • Hydrogen
  • nickel-iron hydrogenase
  • Hydrogenase
  • Urease