Targeted isolation of antibiofilm compounds from halophytic endophyte Bacillus velezensis 7NPB-3B using LC-HR-MS-based metabolomics

Sanju Singh, Elizabeth Nwagwu, Louise Young, Pankaj Kumar, Pramod B. Shinde, RuAngelie Edrada-Ebel

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Abstract

The discovery of new natural products has become more challenging because of the re-isolation of compounds and the lack of new sources. Microbes dwelling in extreme conditions of high salinity and temperature are huge prospects for interesting natural metabolites. In this study, the endophytic bacteria Bacillus velezensis 7NPB-3B isolated from the halophyte Salicornia brachiata was screened for its biofilm inhibition against methicillin-resistant Staphylococcus aureus (MRSA). The fractionation of the crude extract was guided by bioassay and LC-HRMS-based metabolomics using multivariate analysis. The 37 fractions obtained by high-throughput chromatography were dereplicated using an in-house MS-Excel macro coupled with the Dictionary of Natural Products database. Successive bioactivity-guided separation yielded one novel compound (1), a diketopiperazine (m/z 469.258 [M − H]−) with an attached saturated decanoic acid chain, and four known compounds (2–5). The compounds were identified based on 1D- and 2D-NMR and mass spectrometry. Compounds 1 and 5 exhibited excellent biofilm inhibition properties of >90% against the MRSA pathogen at minimum inhibition concentrations of 25 and 35 µg/mL, respectively. The investigation resulted in the isolation of a novel diketopiperazine from a bacterial endophyte of an untapped plant using an omics approach.
Original languageEnglish
Article number413
Number of pages20
JournalMicroorganisms
Volume12
Issue number2
DOIs
Publication statusPublished - 19 Feb 2024

Funding

Financial support was provided by the Newton-Bhabha Placement Program jointly supported by the Department of Biotechnology and the British Council under the Newton-Bhabha fund. S.S. acknowledges the CSIR-JRF fellowship Council of Industrial and Scientific Research (CSIR). P.K. acknowledges the Department of Biotechnology, India for the DBT-JRF fellowship. Department of Pure and Applied Chemistry, University of Strathclyde, and the centralized instrument facility of CSIR-CSMCRI are acknowledged for providing instrumentation facilities. This research was funded by the Newton-Bhabha PhD placement program 2020–2021 (Grant ID: 648104788) funded by the British Council UK and Department of Biotechnology, India. This work was supported by the Scientific and Engineering Research Board (SERB), Department of Science and Technology (Grant ID: ECRA/2016/000788 and EEQ/2016/000268).

Keywords

  • antibiofilm
  • dereplication
  • endophytes
  • halophyte
  • metabolite profiling
  • multivariate analysis

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