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Genome-guided purification of high amounts of the siderophore ornibactin and detection of potentially novel burkholdine derivatives produced by Burkholderia catarinensis 89T.
Bach, Evelise; Chen, Julia; Angolini, Célio Fernando Figueiredo; Bauer, Judith S; Gross, Harald; Passaglia, Luciane Maria Pereira.
Affiliation
  • Bach E; Departamento de Biofísica, Instituto de Biociências, Universidade Federal do Rio Grande do Sul (UFRGS), 91540-000, Porto, Alegre, RS, Brazil.
  • Chen J; Department of Pharmaceutical Biology, Pharmaceutical Institute, University of Tübingen, Tübingen, 72076, Germany.
  • Angolini CFF; Centro de Ciências Naturais e Humanas, Universidade Federal do ABC (UFABC), 09210580, Santo André, SP, Brazil.
  • Bauer JS; Department of Pharmaceutical Biology, Pharmaceutical Institute, University of Tübingen, Tübingen, 72076, Germany.
  • Gross H; Department of Pharmaceutical Biology, Pharmaceutical Institute, University of Tübingen, Tübingen, 72076, Germany.
  • Passaglia LMP; Departamento de Genética, Instituto de Biociências, UFRGS, 91501970, Porto, Alegre, RS, Brazil.
J Appl Microbiol ; 135(2)2024 Feb 01.
Article in En | MEDLINE | ID: mdl-38364306
ABSTRACT

AIM:

The increased availability of genome sequences has enabled the development of valuable tools for the prediction and identification of bacterial natural products. Burkholderia catarinensis 89T produces siderophores and an unknown potent antifungal metabolite. The aim of this work was to identify and purify natural products of B. catarinensis 89T through a genome-guided approach. MATERIALS AND

METHODS:

The analysis of B. catarinensis 89T genome revealed 16 clusters putatively related to secondary metabolism and antibiotics production. Of particular note was the identification of a nonribosomal peptide synthetase (NRPS) cluster related to the production of the siderophore ornibactin, a hybrid NRPS-polyketide synthase Type 1 cluster for the production of the antifungal glycolipopeptide burkholdine, and a gene cluster encoding homoserine lactones (HSL), probably involved in the regulation of both metabolites. We were able to purify high amounts of the ornibactin derivatives D/C6 and F/C8, while also detecting the derivative B/C4 in mass spectrometry investigations. A group of metabolites with molecular masses ranging from 1188 to 1272 Da could be detected in MS experiments, which we postulate to be new burkholdine analogs produced by B. catarinensis. The comparison of B. catarinensis BGCs with other Bcc members corroborates the hypothesis that this bacterium could produce new derivatives of these metabolites. Moreover, the quorum sensing metabolites C6-HSL, C8-HSL, and 3OH-C8-HSL were observed in LC-MS/MS analysis.

CONCLUSION:

The new species B. catarinensis is a potential source of new bioactive secondary metabolites. Our results highlight the importance of genome-guided purification and identification of metabolites of biotechnological importance.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biological Products / 4-Butyrolactone / Burkholderia / Burkholderia cepacia complex / Lipopeptides Language: En Journal: J Appl Microbiol Journal subject: MICROBIOLOGIA Year: 2024 Document type: Article Affiliation country: Brazil Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biological Products / 4-Butyrolactone / Burkholderia / Burkholderia cepacia complex / Lipopeptides Language: En Journal: J Appl Microbiol Journal subject: MICROBIOLOGIA Year: 2024 Document type: Article Affiliation country: Brazil Country of publication: United kingdom