4.7 Article

Genetics and regulation of nitrogen fixation in Paenibacillus brasilensis PB24

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MICROBIOLOGICAL RESEARCH
卷 243, 期 -, 页码 -

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ELSEVIER GMBH
DOI: 10.1016/j.micres.2020.126647

关键词

Paenibacillus brasilensis; Nitrogen fixation; nif genes; Nitrogenase; Regulation

资金

  1. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)
  2. Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES) [001]
  3. Fundacao de Amparo a Pesquisa do Estado do Rio de Janeiro (FAPERJ)

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This study investigated the nitrogen fixation genes of Paenibacillus brasilensis PB24, identifying the nif operon and regulatory genes involved in biological nitrogen fixation. Gene expression analysis revealed that the presence of NH4 affected the expression of structural and regulatory genes in PB24. Furthermore, the regulatory mechanism of GlnR in PB24 differed from other Paenibacillus species, indicating different binding site distributions.
Biological nitrogen fixation (BNF), performed by diazotrophic prokaryotes, is responsible for reducing dinitrogen (N-2) present in the biosphere into biologically available forms of nitrogen. Paenibacillus brasilensis PB24 is a diazotrophic Gram-positive bacterium and is considered ecologically and industrially important because it is able to produce antimicrobial substances and 2,3-butanediol. However, the genetics and regulation of its nitrogen fixing (nif) genes have never been assessed so far. Therefore, the present study aimed to (i) identify the structural and regulatory genes related to BNF in the PB24 genome, (ii) perform comparative genomics analysis of the nif operon among different Paenibacillus species and (iii) study the expression of these genes in the presence and absence of NH4. Strain PB24 showed a nif operon composed of nine genes (nifBHDKENXhesAV), with a conserved synteny (with small variations) among the Paenibacillus species evaluated. BNF regulatory genes, glnK and amtB (encoding GlnK signal transduction protein and AmtB transmembrane protein, respectively) and glnR and glnA genes (encoding the transcription factor GlnR and glutamine synthetase) were found in the PB24 genome. Primers were designed for qPCR amplification of the nitrogenase structural (nifH, nifD and nifK) and regulatory (glnA and amtB) BNF genes. The structural gene expression in PB24 was upand downregulated in the absence and presence of NH4, respectively. The gene expression levels indicated a GlnR-mediated repression of genes associated with ammonium import (amtBglnK) and BNF (nif genes). Additionally, the regulatory mechanism of GlnR in P. brasilensis PB24 differed from the other Paenibacillus evaluated, considering the different distribution of binding sites recognized by GlnR.

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