4.6 Article

XAC4296 Is a Multifunctional and Exclusive Xanthomonadaceae Gene Containing a Fusion of Lytic Transglycosylase and Epimerase Domains

期刊

MICROORGANISMS
卷 10, 期 5, 页码 -

出版社

MDPI
DOI: 10.3390/microorganisms10051008

关键词

citrus canker; multi-domains enzymes; gene fusion; cell wall synthesis; antimicrobial resistance; Xanthomonas citri

资金

  1. Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior-Brasil (CAPES) [001]
  2. Brazilian National Research Council (CNPq)
  3. CAPES
  4. Agronomy (Genetics and Plant Breeding) Graduate Program of the Faculty of Agricultural and Veterinary Sciences (FCAV-UNESP-Jaboticabal)

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This study investigates the role and evolutionary history of a multidomain enzyme, XAC4296, in Xanthomonas citri subsp. citri. The experimental characterization of XAC4296 reveals its expression during plant-pathogen interaction and its impact on Citrus Canker progression. The study also suggests that XAC4296 may contribute to resistance to beta-lactam antibiotics and shows a functional relationship with central carbon and cell wall metabolism. These findings provide new insights into multidomain proteins and antimicrobial resistance in the Xanthomonadaceae family.
Microorganisms have a limited and highly adaptable repertoire of genes capable of encoding proteins containing single or variable multidomains. The phytopathogenic bacteria Xanthomonas citri subsp. citri (X. citri) (Xanthomonadaceae family), the etiological agent of Citrus Canker (CC), presents a collection of multidomain and multifunctional enzymes (MFEs) that remains to be explored. Recent studies have shown that multidomain enzymes that act on the metabolism of the peptidoglycan and bacterial cell wall, belonging to the Lytic Transglycosylases (LTs) superfamily, play an essential role in X. citri biology. One of these LTs, named XAC4296, apart from the Transglycosylase SLT_2 and Peptidoglycan binding-like domains, contains an unexpected aldose 1-epimerase domain linked to the central metabolism; therefore, resembling a canonical MFE. In this work, we experimentally characterized XAC4296 revealing its role as an MFE and demonstrating its probable gene fusion origin and evolutionary history. The XAC4296 is expressed during plant-pathogen interaction, and the Delta 4296 mutant impacts CC progression. Moreover, Delta 4296 exhibited chromosome segregation and cell division errors, and sensitivity to ampicillin, suggesting not only LT activity but also that the XAC4296 may also contribute to resistance to beta-lactams. However, both Delta 4296 phenotypes can be restored when the mutant is supplemented with sucrose or glutamic acid as a carbon and nitrogen source, respectively; therefore, supporting the epimerase domain's functional relationship with the central carbon and cell wall metabolism. Taken together, these results elucidate the role of XAC4296 as an MFE in X. citri, also bringing new insights into the evolution of multidomain proteins and antimicrobial resistance in the Xanthomonadaceae family.

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