Scientific Reports (Dec 2022)

Class II LitR serves as an effector of “short” LOV-type blue-light photoreceptor in Pseudomonas mendocina

  • Takafumi Maruyama,
  • Satoru Sumi,
  • Mitsuru Kobayashi,
  • Teppei Ebuchi,
  • Yu Kanesaki,
  • Hirofumi Yoshikawa,
  • Kenji Ueda,
  • Hideaki Takano

DOI
https://doi.org/10.1038/s41598-022-26254-3
Journal volume & issue
Vol. 12, no. 1
pp. 1 – 16

Abstract

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Abstract PmlR2, a class II LitR/CarH family transcriptional regulator, and PmSB-LOV, a “short” LOV-type blue light photoreceptor, are adjacently encoded in Pseudomonas mendocina NBRC 14162. An effector protein for the “short” LOV-type photoreceptor in Pseudomonas has not yet been identified. Here, we show that PmlR2 is an effector protein of PmSB-LOV. Transcriptional analyses revealed that the expression of genes located near pmlR2 and its homolog gene, pmlR1, was induced in response to illumination. In vitro DNA–protein binding analyses showed that recombinant PmlR2 directly binds to the promoter region of light-inducible genes. Furthermore PmSB-LOV exhibited a typical LOV-type light-induced spectral change. Gel-filtration chromatography demonstrated that the illuminated PmSB-LOV was directly associated with PmlR2, whereas non-illuminated proteins did not interact. The inhibition of PmlR2 function following PmSB-LOV binding was verified by surface plasmon resonance: the DNA-binding ability of PmlR2 was specifically inhibited in the presence of blue light-illuminated-PmSB-LOV. An In vitro transcription assay showed a dose-dependent reduction in PmlR2 repressor activity in the presence of illuminated PmSB-LOV. Overall, evidence suggests that the DNA-binding activity of PmlR2 is inhibited by its direct association with blue light-activated PmSB-LOV, enabling transcription of light-inducible promoters by RNA polymerase.