Autotrophic and mixotrophic hydrogen photoproduction in sulfur-deprived chlamydomonas cells

Appl Environ Microbiol. 2005 Oct;71(10):6199-205. doi: 10.1128/AEM.71.10.6199-6205.2005.

Abstract

In Chlamydomonas reinhardtii cells, H2 photoproduction can be induced in conditions of sulfur deprivation in the presence of acetate. The decrease in photosystem II (PSII) activity induced by sulfur deprivation leads to anoxia, respiration becoming higher than photosynthesis, thereby allowing H2 production. Two different electron transfer pathways, one PSII dependent and the other PSII independent, have been proposed to account for H2 photoproduction. In this study, we investigated the contribution of both pathways as well as the acetate requirement for H2 production in conditions of sulfur deficiency. By using 3-(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU), a PSII inhibitor, which was added at different times after the beginning of sulfur deprivation, we show that PSII-independent H2 photoproduction depends on previously accumulated starch resulting from previous photosynthetic activity. Starch accumulation was observed in response to sulfur deprivation in mixotrophic conditions (presence of acetate) but also in photoautotrophic conditions. However, no H2 production was measured in photoautotrophy if PSII was not inhibited by DCMU, due to the fact that anoxia was not reached. When DCMU was added at optimal starch accumulation, significant H2 production was measured. H2 production was enhanced in autotrophic conditions by removing O2 using N2 bubbling, thereby showing that substantial H2 production can be achieved in the absence of acetate by using the PSII-independent pathway. Based on these data, we discuss the possibilities of designing autotrophic protocols for algal H2 photoproduction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetates / metabolism
  • Acetates / pharmacology
  • Aerobiosis
  • Anaerobiosis
  • Animals
  • Chlamydomonas / growth & development
  • Chlamydomonas / metabolism*
  • Chlamydomonas / physiology
  • Culture Media
  • Diuron / pharmacology
  • Electron Transport
  • Hydrogen / metabolism*
  • Oxygen / metabolism
  • Photosynthesis / physiology*
  • Photosynthetic Reaction Center Complex Proteins
  • Starch / metabolism
  • Sulfur / metabolism*

Substances

  • Acetates
  • Culture Media
  • Photosynthetic Reaction Center Complex Proteins
  • Sulfur
  • Hydrogen
  • Starch
  • Diuron
  • Oxygen