Efficient ammonia oxidation by Pseudomonas citronellolis strain YN-21 under strongly acidic conditions: Performance
Yuran Yang1, Liuyi Chen2, Tuohong Liu1
1Chongqing Key Laboratory of Interface Process and Soil Health, College of Resources and Environment, Southwest University, Chongqing 400716, China.
Abstract:
Ammonia oxidation microorganisms generally tend to have low rates of ammonia oxidation under acidic conditions, as the protonated ammonia is not a substrate for ammonia monooxygenase. In this work, heterotrophic ammonia oxidation bacteria (HAOB) Pseudomonas citronellolis strain YN-21 showed high efficiency in removing NH4+ (12.7 mg/L/h) even at initial pH 4.5. The potential acid resistance mechanisms (H+ efflux, H+ consumption, and production of alkaline substances) maintained intracellular pH neutrality. Transcriptome analysis showed that genes involved in amino acid metabolism, carbohydrate metabolism, ABC transporter and nitrogen metabolism were significantly up-regulated, which facilitated the rapid removal of NH4+ in an acidic environment. Moreover, urea could be used as an alternative nitrogen source for YN-21 in a strongly acidic environment, and the production of NH3 from urea hydrolysis provided a substrate for ammonia oxidation. These results provide new insights into efficient ammonia oxidation in acidic environments.
Related Concept Videos
Metabolism of Chemolithotrophs
Titration of a Weak Base with a Strong Acid
Using the ICE table and substituting the Kb value, we calculate the initial pH of 50 mL of 0.1 M ammonia to be 11.11. Addition of 25 mL of 0.1 M hydrochloric acid to this solution of ammonia results in a buffer with an equal concentration of ammonia and ammonium ions. The pH of this buffer can be calculated by substituting these...
Titration of a Weak Acid with a Weak Base
As a result, there is no simple...
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...
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Mechanism
Common Ion Effect


