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Exploring bioactive peptides from bacterial secretomes using PepSAVI‐MS: identification and characterization of Bac‐21 from Enterococcus faecalis pPD1

As current methods for antibiotic drug discovery are being outpaced by the rise of antimicrobial resistance, new methods and innovative technologies are necessary to replenish our dwindling arsenal of antimicrobial agents. To this end, we developed the PepSAVI‐MS pipeline to expedite the search for...

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Autores principales: Kirkpatrick, Christine L., Parsley, Nicole C., Bartges, Tessa E., Wing, Casey E., Kommineni, Sushma, Kristich, Christopher J., Salzman, Nita H., Patrie, Steven M., Hicks, Leslie M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6116741/
https://www.ncbi.nlm.nih.gov/pubmed/30014612
http://dx.doi.org/10.1111/1751-7915.13299
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author Kirkpatrick, Christine L.
Parsley, Nicole C.
Bartges, Tessa E.
Wing, Casey E.
Kommineni, Sushma
Kristich, Christopher J.
Salzman, Nita H.
Patrie, Steven M.
Hicks, Leslie M.
author_facet Kirkpatrick, Christine L.
Parsley, Nicole C.
Bartges, Tessa E.
Wing, Casey E.
Kommineni, Sushma
Kristich, Christopher J.
Salzman, Nita H.
Patrie, Steven M.
Hicks, Leslie M.
author_sort Kirkpatrick, Christine L.
collection PubMed
description As current methods for antibiotic drug discovery are being outpaced by the rise of antimicrobial resistance, new methods and innovative technologies are necessary to replenish our dwindling arsenal of antimicrobial agents. To this end, we developed the PepSAVI‐MS pipeline to expedite the search for natural product bioactive peptides. Herein we demonstrate expansion of PepSAVI‐MS for the discovery of bacterial‐sourced bioactive peptides through identification of the bacteriocin Bac‐21 from Enterococcus faecalis pPD1. Minor pipeline modifications including implementation of bacteria‐infused agar diffusion assays and optional digestion of peptide libraries highlight the versatility and wide adaptability of the PepSAVI‐MS pipeline. Additionally, we have experimentally validated the primary protein sequence of the active, mature Bac‐21 peptide for the first time and have confirmed its identity with respect to primary sequence and post‐translational processing. Successful application of PepSAVI‐MS to bacterial secretomes as demonstrated herein establishes proof‐of‐principle for use in novel microbial bioactive peptide discovery.
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spelling pubmed-61167412018-09-05 Exploring bioactive peptides from bacterial secretomes using PepSAVI‐MS: identification and characterization of Bac‐21 from Enterococcus faecalis pPD1 Kirkpatrick, Christine L. Parsley, Nicole C. Bartges, Tessa E. Wing, Casey E. Kommineni, Sushma Kristich, Christopher J. Salzman, Nita H. Patrie, Steven M. Hicks, Leslie M. Microb Biotechnol Research Articles As current methods for antibiotic drug discovery are being outpaced by the rise of antimicrobial resistance, new methods and innovative technologies are necessary to replenish our dwindling arsenal of antimicrobial agents. To this end, we developed the PepSAVI‐MS pipeline to expedite the search for natural product bioactive peptides. Herein we demonstrate expansion of PepSAVI‐MS for the discovery of bacterial‐sourced bioactive peptides through identification of the bacteriocin Bac‐21 from Enterococcus faecalis pPD1. Minor pipeline modifications including implementation of bacteria‐infused agar diffusion assays and optional digestion of peptide libraries highlight the versatility and wide adaptability of the PepSAVI‐MS pipeline. Additionally, we have experimentally validated the primary protein sequence of the active, mature Bac‐21 peptide for the first time and have confirmed its identity with respect to primary sequence and post‐translational processing. Successful application of PepSAVI‐MS to bacterial secretomes as demonstrated herein establishes proof‐of‐principle for use in novel microbial bioactive peptide discovery. John Wiley and Sons Inc. 2018-07-16 /pmc/articles/PMC6116741/ /pubmed/30014612 http://dx.doi.org/10.1111/1751-7915.13299 Text en © 2018 The Authors. Microbial Biotechnology published by John Wiley & Sons Ltd and Society for Applied Microbiology. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Kirkpatrick, Christine L.
Parsley, Nicole C.
Bartges, Tessa E.
Wing, Casey E.
Kommineni, Sushma
Kristich, Christopher J.
Salzman, Nita H.
Patrie, Steven M.
Hicks, Leslie M.
Exploring bioactive peptides from bacterial secretomes using PepSAVI‐MS: identification and characterization of Bac‐21 from Enterococcus faecalis pPD1
title Exploring bioactive peptides from bacterial secretomes using PepSAVI‐MS: identification and characterization of Bac‐21 from Enterococcus faecalis pPD1
title_full Exploring bioactive peptides from bacterial secretomes using PepSAVI‐MS: identification and characterization of Bac‐21 from Enterococcus faecalis pPD1
title_fullStr Exploring bioactive peptides from bacterial secretomes using PepSAVI‐MS: identification and characterization of Bac‐21 from Enterococcus faecalis pPD1
title_full_unstemmed Exploring bioactive peptides from bacterial secretomes using PepSAVI‐MS: identification and characterization of Bac‐21 from Enterococcus faecalis pPD1
title_short Exploring bioactive peptides from bacterial secretomes using PepSAVI‐MS: identification and characterization of Bac‐21 from Enterococcus faecalis pPD1
title_sort exploring bioactive peptides from bacterial secretomes using pepsavi‐ms: identification and characterization of bac‐21 from enterococcus faecalis ppd1
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6116741/
https://www.ncbi.nlm.nih.gov/pubmed/30014612
http://dx.doi.org/10.1111/1751-7915.13299
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