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Identification of xenobiotic response element family transcription regulator SadR from sulfonamides-degrading strain Microbacterium sp. HA-8 and construction of biosensor to detect sulfonamides. | LitMetric

Identification of xenobiotic response element family transcription regulator SadR from sulfonamides-degrading strain Microbacterium sp. HA-8 and construction of biosensor to detect sulfonamides.

Bioresour Technol

Department of Microbiology, College of Life Sciences, Nanjing Agricultural University, Key Laboratory of Agricultural and Environmental Microbiology, Ministry of Agriculture and Rural Affairs, Nanjing 210095, China. Electronic address:

Published: January 2025

AI Article Synopsis

  • This study focuses on understanding how sulfonamides (SAs) are broken down in the environment by investigating the microbial strain Microbacterium sp. HA-8 that has specific genes for SAs degradation.
  • It identifies SadR as a new regulatory protein that negatively controls the expression of the degradation genes sadAB by binding to their promoter region, but SAs can prevent this binding, thus promoting their own degradation.
  • Additionally, the researchers created a biosensor using E. coli to detect SAs, which showed a reliable response to different concentrations of SAs, paving the way for future environmental monitoring techniques.

Article Abstract

Deciphering the regulatory mechanisms of sulfonamides (SAs) metabolism will contribute to a deeper understanding of SAs degradation in the environment. In this study, a SAs-degrading strain Microbacterium sp. HA-8 harboring a highly conserved SAs-degrading genes sadABC was isolated. SadR was a newly discovered regulator, belonging to xenobiotic response element (XRE) family, which negatively regulated the transcription of sadAB genes. Specifically, SadR bound to the sadA promoter region to repress the expression of sadAB genes. While, SAs prevented SadR from binding to sadA promoter to induce the expression of sadAB genes. Then, a whole-cell biosensor, Escherichia coli DH5α/pSRmCherry was constructed to detect SAs. The dose-dependent fluorescence of the biosensor exhibited a good fit to Hill equation. In summary, this study revealed the regulatory mechanism of SAs degradation in strain HA-8 and developed an innovative biosensor technique for detecting SAs, holding promise for future applications in environmental monitoring.

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Source
http://dx.doi.org/10.1016/j.biortech.2024.131705DOI Listing

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