Abstract

Under starvation conditions, bacteria could consume intracellular macromolecules, which deteriorates the performance of the bioreactor. However, the fundamental endogenous metabolism of anaerobic ammonium oxidation (anammox) bacteria is poorly understood. Here, we describe the endogenous metabolism of anammox bacteria biomass under short-term anaerobic and anoxic starvation stress (4.5d and 40h, respectively) by protein, mRNA and biochemical analyses. The live/dead staining results showed negligible cell death rates. The activity decay rates (decrease in specific activity of active bacteria) were 0.128d−1 and 0.629d−1 under anaerobic and anoxic starvation conditions, respectively. The degradation rates of extracellular polymeric substances (EPS) and hydrazine dehydrogenase protein (HDH) were approximately 4- and 5-fold higher under anoxic starvation than under anaerobic starvation tests, suggesting the electron-donor roles for EPS and HDH in denitrification. The greater consumption of intracellular macromolecules during anoxic starvation corresponded with the greater decrease in anammox activities under this condition. Under both starvation conditions, the mRNA decay rates of nirS, hzsA, and hdh mRNA (representing metabolic stability) of anammox bacteria decreased from their normal levels. Such control of specific mRNAs is important for economizing protein synthesis and aids the cells’ recovery after starvation stress. These identified endogenous characteristics of anammox bacteria provide new insights into starvation stress responses at the transcriptional and translational levels, and will assist the optimization of anammox processes in bioreactors, which frequently experience starvation conditions.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.