Nature Communications (Apr 2023)

Targeted and high-throughput gene knockdown in diverse bacteria using synthetic sRNAs

  • Jae Sung Cho,
  • Dongsoo Yang,
  • Cindy Pricilia Surya Prabowo,
  • Mohammad Rifqi Ghiffary,
  • Taehee Han,
  • Kyeong Rok Choi,
  • Cheon Woo Moon,
  • Hengrui Zhou,
  • Jae Yong Ryu,
  • Hyun Uk Kim,
  • Sang Yup Lee

DOI
https://doi.org/10.1038/s41467-023-38119-y
Journal volume & issue
Vol. 14, no. 1
pp. 1 – 13

Abstract

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Abstract Synthetic sRNAs allow knockdown of target genes at translational level, but have been restricted to a limited number of bacteria. Here, we report the development of a broad-host-range synthetic sRNA (BHR-sRNA) platform employing the RoxS scaffold and the Hfq chaperone from Bacillus subtilis. BHR-sRNA is tested in 16 bacterial species including commensal, probiotic, pathogenic, and industrial bacteria, with >50% of target gene knockdown achieved in 12 bacterial species. For medical applications, virulence factors in Staphylococcus epidermidis and Klebsiella pneumoniae are knocked down to mitigate their virulence-associated phenotypes. For metabolic engineering applications, high performance Corynebacterium glutamicum strains capable of producing valerolactam (bulk chemical) and methyl anthranilate (fine chemical) are developed by combinatorial knockdown of target genes. A genome-scale sRNA library covering 2959 C. glutamicum genes is constructed for high-throughput colorimetric screening of indigoidine (natural colorant) overproducers. The BHR-sRNA platform will expedite engineering of diverse bacteria of both industrial and medical interest.