Simultaneous quantum yield measurements of carbon uptake and oxygen evolution in microalgal cultures

PLoS One. 2018 Jun 19;13(6):e0199125. doi: 10.1371/journal.pone.0199125. eCollection 2018.

Abstract

The photosynthetic quantum yield (Φ), defined as carbon fixed or oxygen evolved per unit of light absorbed, is a fundamental but rarely determined biophysical parameter. A method to estimate Φ for both net carbon uptake and net oxygen evolution simultaneously can provide important insights into energy and mass fluxes. Here we present details for a novel system that allows quantification of carbon fluxes using pH oscillation and simultaneous oxygen fluxes by integration with a membrane inlet mass spectrometer. The pHOS system was validated using Phaeodactylum tricornutum cultured with continuous illumination of 110 μmole quanta m-2 s-1 at 25°C. Furthermore, simultaneous measurements of carbon and oxygen flux using the pHOS-MIMS and photon flux based on spectral absorption were carried out to explore the kinetics of Φ in P. tricornutum during its acclimation from low to high light (110 to 750 μmole quanta m-2 s-1). Comparing results at 0 and 24 hours, we observed strong decreases in cellular chlorophyll a (0.58 to 0.21 pg cell-1), Fv/Fm (0.71 to 0.59) and maximum ΦCO2 (0.019 to 0.004) and ΦO2 (0.028 to 0.007), confirming the transition toward high light acclimation. The Φ time-series indicated a non-synchronized acclimation response between carbon uptake and oxygen evolution, which has been previously inferred based on transcriptomic changes for a similar experimental design with the same diatom that lacked physiological data. The integrated pHOS-MIMS system can provide simultaneous carbon and oxygen measurements accurately, and at the time-resolution required to resolve high-resolution carbon and oxygen physiological dynamics.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Acclimatization
  • Calibration
  • Carbon / metabolism*
  • Chlorophyll A / metabolism
  • Dose-Response Relationship, Radiation
  • Equipment Design
  • Hydrogen-Ion Concentration*
  • Light
  • Limit of Detection
  • Mass Spectrometry / instrumentation
  • Mass Spectrometry / methods*
  • Oxygen / metabolism*
  • Photosynthesis* / radiation effects
  • Photosystem II Protein Complex / metabolism
  • Photosystem II Protein Complex / radiation effects
  • Stramenopiles / metabolism*
  • Stramenopiles / radiation effects

Substances

  • Photosystem II Protein Complex
  • Carbon
  • Oxygen
  • Chlorophyll A

Grants and funding

This work was supported by the U.S. Department of Energy (DE-SC0008593) to Dr. Andrew E. Allen; U.S. Department of Energy (DE-EE0003373) to Dr. B. Greg Mitchell, Dr. Andrew Allen and Dr. Christopher L. DuPont; Gordon and Betty Moore Foundation (GMBF3828) to Dr. Andrew E. Allen; Edna Bailey Sussman Foundation to Dr. Niu Du; and Robert Buzzelli Endowed Fellowship to Dr. Niu Du. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.