The copper-responsive regulator CsoR is indirectly involved in Bradyrhizobium diazoefficiens denitrification

FEMS Microbiol Lett. 2023 Jan 17:370:fnad084. doi: 10.1093/femsle/fnad084.

Abstract

The soybean endosymbiont Bradyrhizobium diazoefficiens harbours the complete denitrification pathway that is catalysed by a periplasmic nitrate reductase (Nap), a copper (Cu)-containing nitrite reductase (NirK), a c-type nitric oxide reductase (cNor), and a nitrous oxide reductase (Nos), encoded by the napEDABC, nirK, norCBQD, and nosRZDFYLX genes, respectively. Induction of denitrification genes requires low oxygen and nitric oxide, both signals integrated into a complex regulatory network comprised by two interconnected cascades, FixLJ-FixK2-NnrR and RegSR-NifA. Copper is a cofactor of NirK and Nos, but it has also a role in denitrification gene expression and protein synthesis. In fact, Cu limitation triggers a substantial down-regulation of nirK, norCBQD, and nosRZDFYLX gene expression under denitrifying conditions. Bradyrhizobium diazoefficiens genome possesses a gene predicted to encode a Cu-responsive repressor of the CsoR family, which is located adjacent to copA, a gene encoding a putative Cu+-ATPase transporter. To investigate the role of CsoR in the control of denitrification gene expression in response to Cu, a csoR deletion mutant was constructed in this work. Mutation of csoR did not affect the capacity of B. diazoefficiens to grow under denitrifying conditions. However, by using qRT-PCR analyses, we showed that nirK and norCBQD expression was much lower in the csoR mutant compared to wild-type levels under Cu-limiting denitrifying conditions. On the contrary, copA expression was significantly increased in the csoR mutant. The results obtained suggest that CsoR acts as a repressor of copA. Under Cu limitation, CsoR has also an indirect role in the expression of nirK and norCBQD genes.

Keywords: Cu-responsive regulator; gene expression; nitric oxide reductase; nitrite reductase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Bradyrhizobium* / genetics
  • Bradyrhizobium* / metabolism
  • Copper* / metabolism
  • Denitrification
  • Gene Expression Regulation, Bacterial
  • Nitrates / metabolism
  • Nitrite Reductases / genetics
  • Nitrite Reductases / metabolism

Substances

  • Copper
  • Nitrite Reductases
  • Nitrates
  • Bacterial Proteins

Supplementary concepts

  • Bradyrhizobium diazoefficiens