Dark Respiration Measurement from Arabidopsis Shoots

Jose P Fonseca; Marcus Griffiths; Larry M York; Kirankumar S Mysore

doi:10.21769/BioProtoc.4181

Dark Respiration Measurement from Arabidopsis Shoots

Bio Protoc. 2021 Oct 5;11(19):e4181. doi: 10.21769/BioProtoc.4181.

Authors

Jose P Fonseca¹, Marcus Griffiths¹, Larry M York¹, Kirankumar S Mysore^{1

2

3}

Affiliations

¹ Noble Research Institute, LLC., Ardmore, OK, USA.
² Institute for Agricultural Biosciences, Oklahoma State University, Ardmore, OK, 73401, USA.
³ Department of Biochemistry and Molecular Biology, Oklahoma State University, Stillwater, OK, 74078, USA.

Abstract

Dark respiration refers to experimental measures of leaf respiration in the absence of light, done to distinguish it from the photorespiration that occurs during photosynthesis. Dark aerobic respiration reactions occur solely in the mitochondria and convert glucose molecules from cytoplasmatic glycolysis and oxygen into carbon dioxide and water, with the generation of ATP molecules. Previous methods typically use oxygen sensors to measure oxygen depletion or complicated and expensive photosynthesis instruments to measure CO₂ accumulation. Here, we provide a detailed, step-by-step approach to measure dark respiration in plants by recording CO₂ fluxes of Arabidopsis shoot and root tissues. Briefly, plants are dark acclimated for 1 hour, leaves and roots are excised and placed separately in airtight chambers, and CO₂ accumulation is measured over time with standard infrared gas analyzers. The time-series data is processed with R scripts to produce dark respiration rates, which can be standardized by fresh or dry tissue mass. The current method requires inexpensive infrared gas analyzers, off-the-shelf parts for chambers, and publicly available data analysis scripts.

Keywords: CO2; Mitochondria; Dark respiration; Flux; NFS1.