Quantitative proteomic and transcriptional analyses reveal degradation pathway of γ-hexachlorocyclohexane and the metabolic context in the actinobacterium Streptomyces sp. M7

Chemosphere. 2018 Nov:211:1025-1034. doi: 10.1016/j.chemosphere.2018.08.035. Epub 2018 Aug 10.

Abstract

Highly contaminated γ-hexachlorocyclohexane (lindane) areas were reported worldwide. Low aqueous solubility and high hydrophobicity make lindane particularly resistant to microbial degradation. Physiological and genetic Streptomyces features make this genus more appropriate for bioremediation compared with others. Complete degradation of lindane was only proposed in the genus Sphingobium although the metabolic context of the degradation was not considered. Streptomyces sp.M7 has demonstrated ability to remove lindane from culture media and soils. In this study, we used MS-based label-free quantitative proteomic, RT-qPCR and exhaustive bioinformatic analysis to understand lindane degradation and its metabolic context in Streptomyces sp. M7. We identified the proteins involved in the up-stream degradation pathway. In addition, results demonstrated that mineralization of lindane is feasible since proteins from an unusual down-stream degradation pathway were also identified. Degradative steps were supported by an active catabolism that supplied energy and reducing equivalents in the form of NADPH. To our knowledge, this is the first study in which degradation steps of an organochlorine compound and metabolic context are elucidate in a biotechnological genus as Streptomyces. These results serve as basement to study other degradative actinobacteria and to improve the degradation processes of Streptomyces sp. M7.

Keywords: Lindane degradation; Metabolism; Proteomics; Streptomyces.

MeSH terms

  • Biodegradation, Environmental
  • Hexachlorocyclohexane / metabolism*
  • Metabolic Networks and Pathways*
  • Proteome / analysis
  • Proteome / metabolism*
  • Proteomics / methods*
  • Streptomyces / genetics*
  • Streptomyces / metabolism*
  • Transcriptome*

Substances

  • Proteome
  • Hexachlorocyclohexane