Acetylene reduction assay for nitrogenase activity in root nodules under salinity stress
Liping Gu1, Jesus Raul Loya2, Senthil Subramanian3
1Department of Biology and Microbiology, South Dakota State University, Brookings, SD, United States.
This study details a method to measure nitrogenase activity in field peas using the acetylene reduction assay under saline stress. This research supports understanding biological nitrogen fixation in crops facing environmental challenges.
Area of Science:
- Biochemistry
- Environmental Science
- Agricultural Science
Background:
- Nitrogenase catalyzes nitrogen fixation, converting N2 to NH3, vital for the N cycle.
- Biological nitrogen fixation by rhizobia in legumes is crucial for sustainable agriculture.
- Climate change necessitates evaluating crop stress impacts on nitrogen fixation.
Purpose of the Study:
- To provide a detailed protocol for measuring nitrogenase activity.
- To assess nitrogenase activity in field pea root nodules under saline stress.
- To offer an adaptable method for other biological systems.
Main Methods:
- Utilized the acetylene reduction assay to measure nitrogenase activity.
- Applied saline stress conditions to field pea plants.
- Developed a step-by-step protocol for the assay.
Main Results:
- Successfully measured nitrogenase activity in field pea root nodules.
- Demonstrated the application of the acetylene reduction assay under saline stress.
- Established a reproducible protocol for nitrogenase measurement.
Conclusions:
- The acetylene reduction assay is a reliable method for assessing nitrogenase activity in legumes under stress.
- This protocol aids in evaluating the impact of environmental stressors on biological nitrogen fixation.
- The method can be adapted for diverse plant-microbe systems facing environmental challenges.
Related Concept Videos
Inorganic Nitrogen Assimilation
Responses to Salt Stress
2° Amines to N-Nitrosamines: Reaction with NaNO2
Reduction of Alkynes to trans-Alkenes: Sodium in Liquid Ammonia
When dissolved in liquid ammonia, an alkali metal,...
Preparation of Amines: Reduction of Oximes and Nitro Compounds
Though catalytic hydrogenation can reduce nitrobenzenes, the reduction is nonselective in the presence of other functional groups. For instance, if nitrobenzene contains an aldehyde group,...
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Overview
The nitrous acid is unstable. Hence, it is formed in situ from a solution of sodium nitrite and cold aqueous acids such as hydrochloric or sulfuric acid. In an acidic solution, the –OH group of nitrous acid undergoes protonation to give oxonium ion, followed by...


