Article ID Journal Published Year Pages File Type
5758867 Water Research 2017 8 Pages PDF
Abstract

•E1 degradation rate was higher with NH4+ than with NO3− as the nitrogen source.•E1 degradation rate was higher when acetic acid or humic acid was present in the background.•Tyrosine metabolism might play an important role in E1 biodegradation.•NH4+ promoted the tyrosine synthesis by promoting the GS-GOGAT pathway.•Background carbon substrates triggered the up-regulation of tyrosine metabolism.

Microbial degradation of estrogenic compounds can be affected by the nitrogen source and background carbon in the environment. However, the underlying mechanisms are not well understood. The objective of this study was to elucidate the molecular mechanisms of estrone (E1) biodegradation at the protein level under various background nitrogen (nitrate or ammonium) and carbon conditions (no background carbon, acetic acid, or humic acid as background carbon) by a newly isolated bacterial strain. The E1 degrading bacterial strain, Hydrogenophaga atypica ZD1, was isolated from river sediments and its proteome was characterized under various experimental conditions using quantitative proteomics. Results show that the E1 degradation rate was faster when ammonium was used as the nitrogen source than with nitrate. The degradation rate was also faster when either acetic acid or humic acid was present in the background. Proteomics analyses suggested that the E1 biodegradation products enter the tyrosine metabolism pathway. Compared to nitrate, ammonium likely promoted E1 degradation by increasing the activities of the branched-chain-amino-acid aminotransferase (IlvE) and enzymes involved in the glutamine synthetase-glutamine oxoglutarate aminotransferase (GS-GOGAT) pathway. The increased E1 degradation rate with acetic acid or humic acid in the background can also be attributed to the up-regulation of IlvE. Results from this study can help predict and explain E1 biodegradation kinetics under various environmental conditions.

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Related Topics
Physical Sciences and Engineering Earth and Planetary Sciences Earth-Surface Processes
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