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Distribution and diversity of dimetal-carboxylate halogenases in cyanobacteria.
Eusebio, Nadia; Rego, Adriana; Glasser, Nathaniel R; Castelo-Branco, Raquel; Balskus, Emily P; Leão, Pedro N.
Afiliación
  • Eusebio N; Interdisciplinary Centre of Marine and Environmental Research (CIIMAR/CIMAR), University of Porto, Matosinhos, Portugal.
  • Rego A; Interdisciplinary Centre of Marine and Environmental Research (CIIMAR/CIMAR), University of Porto, Matosinhos, Portugal.
  • Glasser NR; Department of Chemistry and Chemical Biology, Harvard University, Cambridge, MA, USA.
  • Castelo-Branco R; Interdisciplinary Centre of Marine and Environmental Research (CIIMAR/CIMAR), University of Porto, Matosinhos, Portugal.
  • Balskus EP; Department of Chemistry and Chemical Biology, Harvard University, Cambridge, MA, USA. balskus@chemistry.harvard.edu.
  • Leão PN; Interdisciplinary Centre of Marine and Environmental Research (CIIMAR/CIMAR), University of Porto, Matosinhos, Portugal. pleao@ciimar.up.pt.
BMC Genomics ; 22(1): 633, 2021 Aug 31.
Article en En | MEDLINE | ID: mdl-34461836
BACKGROUND: Halogenation is a recurring feature in natural products, especially those from marine organisms. The selectivity with which halogenating enzymes act on their substrates renders halogenases interesting targets for biocatalyst development. Recently, CylC - the first predicted dimetal-carboxylate halogenase to be characterized - was shown to regio- and stereoselectively install a chlorine atom onto an unactivated carbon center during cylindrocyclophane biosynthesis. Homologs of CylC are also found in other characterized cyanobacterial secondary metabolite biosynthetic gene clusters. Due to its novelty in biological catalysis, selectivity and ability to perform C-H activation, this halogenase class is of considerable fundamental and applied interest. The study of CylC-like enzymes will provide insights into substrate scope, mechanism and catalytic partners, and will also enable engineering these biocatalysts for similar or additional C-H activating functions. Still, little is known regarding the diversity and distribution of these enzymes. RESULTS: In this study, we used both genome mining and PCR-based screening to explore the genetic diversity of CylC homologs and their distribution in bacteria. While we found non-cyanobacterial homologs of these enzymes to be rare, we identified a large number of genes encoding CylC-like enzymes in publicly available cyanobacterial genomes and in our in-house culture collection of cyanobacteria. Genes encoding CylC homologs are widely distributed throughout the cyanobacterial tree of life, within biosynthetic gene clusters of distinct architectures (combination of unique gene groups). These enzymes are found in a variety of biosynthetic contexts, which include fatty-acid activating enzymes, type I or type III polyketide synthases, dialkylresorcinol-generating enzymes, monooxygenases or Rieske proteins. Our study also reveals that dimetal-carboxylate halogenases are among the most abundant types of halogenating enzymes in the phylum Cyanobacteria. CONCLUSIONS: Our data show that dimetal-carboxylate halogenases are widely distributed throughout the Cyanobacteria phylum and that BGCs encoding CylC homologs are diverse and mostly uncharacterized. This work will help guide the search for new halogenating biocatalysts and natural product scaffolds.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteínas Bacterianas / Cianobacterias Límite: Humans Idioma: En Revista: BMC Genomics Asunto de la revista: GENETICA Año: 2021 Tipo del documento: Article País de afiliación: Portugal

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteínas Bacterianas / Cianobacterias Límite: Humans Idioma: En Revista: BMC Genomics Asunto de la revista: GENETICA Año: 2021 Tipo del documento: Article País de afiliación: Portugal