4.3 Article

Characterization and Degradation Pathways of Microbacterium resistens MZT7, A Novel 17β-Estradiol-Degrading Bacterium

Publisher

MDPI
DOI: 10.3390/ijerph191711097

Keywords

17 beta-estradiol; Microbacterium resistens MZT7; biodegradation; metabolic pathway; genome analyses

Funding

  1. Strategic Priority Research Program of the Chinese Academy of Sciences [XDA28080400]
  2. Jilin Province Science and Technology Development Plan Project [20190201296JC]
  3. Tibet Autonomous Region Science and Technology Project [XZ202101ZD0002N-04]
  4. China Agriculture Research System of MOF and MARA [CARS-37]

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A highly efficient E2-degrading bacterial strain, Microbacterium resistens MZT7, was isolated and characterized. The strain showed excellent adaptability and degradation efficiency towards E2. Three metabolic pathways were proposed and one pathway was confirmed through gene identification. This study provides important insights into the degradation of E2.
Due to the ecotoxicity of 17 beta-estradiol (E2), residual E2 in the environment poses potential risks to human and animal health and ecosystems. Biodegradation is considered one of the most effective strategies to remove E2 from the environment. Here, a novel, efficient E2-degrading bacterial strain Microbacterium resistens MZT7 was isolated from activated sludge and characterized. The genome of strain MZT7 contained 4,011,347 bp nucleotides with 71.26% G + C content and 3785 coding genes. There was 86.7% transformation efficiency of 10 mg/L E2 by strain MZT7 after incubation for 5 d at optimal temperature (30 degrees C) and pH (7.0). This strain was highly tolerant to ranges in pH (5.0-11.0), temperature (20-40 degrees C), and salinity (2-8%). Adding sources of carbon (glucose, maltose, sucrose, or lactose) or nitrogen sources (urea, peptone, or beef extract) promoted the degradation of E2 by strain MZT7. However, when yeast extract was added as a nitrogen source, the degradation efficiency of E2 was inhibited. Metabolites were analyzed by LC-MS and three metabolic pathways of E2 degradation were proposed. Further, the intermediates dehydroepiandrosterone and androsta-1,4-diene-3,17-dione were detected, as well as identification of kshB and fadD3 genes by KEGG, confirming one E2 degradation pathway. This study provided some insights into E2 biodegradation.

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