4.8 Article

Deciphering chloramphenicol biotransformation mechanisms and microbial interactions via integrated multi-omics and cultivation-dependent approaches

期刊

MICROBIOME
卷 10, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s40168-022-01361-5

关键词

Chloramphenicol biotransformation; Multi-omics; Genomics; Metagenomics; Metatranscriptomics; Proteomics; Interspecies interaction

资金

  1. National Key R&D Program of China [2022YFE0103200]
  2. National Natural Science Foundation of China [22176107]
  3. Guangdong Basic and Applied Basic Research Foundation [2019B151502034, 2021A1515110772]
  4. China Postdoctoral Science Foundation [2021M691772]

向作者/读者索取更多资源

This study elucidates the comprehensive biotransformation pathway, key metabolic enzymes, and interspecies interactions of chloramphenicol in an activated sludge-enriched consortium using integrated multi-omics and cultivation-based approaches. The discovery of a new biotransformation pathway and key enzymes, as well as the understanding of synergistic interactions and substrate exchange among microbes, provides valuable resources and knowledge for enhanced bioremediation of chloramphenicol-contaminated sites and environmental microbiology.
Background: As a widely used broad-spectrum antibiotic, chloramphenicol is prone to be released into environments, thus resulting in the disturbance of ecosystem stability as well as the emergence of antibiotic resistance genes. Microbes play a vital role in the decomposition of chloramphenicol in the environment, and the biotransformation processes are especially dependent on synergistic interactions and metabolite exchanges among microbes. Herein, the comprehensive chloramphenicol biotransformation pathway, key metabolic enzymes, and interspecies interactions in an activated sludge-enriched consortium were elucidated using integrated multi-omics and cultivation-based approaches. Results: The initial biotransformation steps were the oxidization at the C-1-OH and C-3-OH groups, the isomerization at C-2, and the acetylation at C-3-OH of chloramphenicol. Among them, the isomerization is an entirely new biotransformation pathway of chloramphenicol discovered for the first time. Furthermore, we identified a novel glucose-methanol-choline oxidoreductase responsible for the oxidization of the C-3-OH group in Sphingomonas sp. and Caballeronia sp. Moreover, the subsequent biotransformation steps, corresponding catalyzing enzymes, and the microbial players responsible for each step were deciphered. Synergistic interactions between Sphingomonas sp. and Caballeronia sp. or Cupriavidus sp. significantly promoted chloramphenicol mineralization, and the substrate exchange interaction network occurred actively among key microbes. Conclusion: This study provides desirable strain and enzyme resources for enhanced bioremediation of chloramphenicol-contaminated hotspot sites such as pharmaceutical wastewater and livestock and poultry wastewater. The in-depth understanding of the chloramphenicol biotransformation mechanisms and microbial interactions will not only guide the bioremediation of organic pollutants but also provide valuable knowledge for environmental microbiology and biotechnological exploitation.

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