Cargando…
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...
Autores principales: | , , , , , , , , |
---|---|
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 |
_version_ | 1783351649118453760 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6116741 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT kirkpatrickchristinel exploringbioactivepeptidesfrombacterialsecretomesusingpepsavimsidentificationandcharacterizationofbac21fromenterococcusfaecalisppd1 AT parsleynicolec exploringbioactivepeptidesfrombacterialsecretomesusingpepsavimsidentificationandcharacterizationofbac21fromenterococcusfaecalisppd1 AT bartgestessae exploringbioactivepeptidesfrombacterialsecretomesusingpepsavimsidentificationandcharacterizationofbac21fromenterococcusfaecalisppd1 AT wingcaseye exploringbioactivepeptidesfrombacterialsecretomesusingpepsavimsidentificationandcharacterizationofbac21fromenterococcusfaecalisppd1 AT komminenisushma exploringbioactivepeptidesfrombacterialsecretomesusingpepsavimsidentificationandcharacterizationofbac21fromenterococcusfaecalisppd1 AT kristichchristopherj exploringbioactivepeptidesfrombacterialsecretomesusingpepsavimsidentificationandcharacterizationofbac21fromenterococcusfaecalisppd1 AT salzmannitah exploringbioactivepeptidesfrombacterialsecretomesusingpepsavimsidentificationandcharacterizationofbac21fromenterococcusfaecalisppd1 AT patriestevenm exploringbioactivepeptidesfrombacterialsecretomesusingpepsavimsidentificationandcharacterizationofbac21fromenterococcusfaecalisppd1 AT hickslesliem exploringbioactivepeptidesfrombacterialsecretomesusingpepsavimsidentificationandcharacterizationofbac21fromenterococcusfaecalisppd1 |