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Efflux pump-deficient mutants as a platform to search for microbes that produce antibiotics
Pseudomonas putida DOT-T1E-18 is a strain deficient in the major antibiotic efflux pump (TtgABC) that exhibits an overall increased susceptibility to a wide range of drugs when compared with the wild-type strain. We used this strain as a platform to search for microbes able to produce antibiotics th...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4476826/ https://www.ncbi.nlm.nih.gov/pubmed/26059350 http://dx.doi.org/10.1111/1751-7915.12295 |
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author | Molina-Santiago, Carlos Udaondo, Zulema Daddaoua, Abdelali Roca, Amalia Martín, Jesús Pérez-Victoria, Ignacio Reyes, Fernando Ramos, Juan-Luis |
author_facet | Molina-Santiago, Carlos Udaondo, Zulema Daddaoua, Abdelali Roca, Amalia Martín, Jesús Pérez-Victoria, Ignacio Reyes, Fernando Ramos, Juan-Luis |
author_sort | Molina-Santiago, Carlos |
collection | PubMed |
description | Pseudomonas putida DOT-T1E-18 is a strain deficient in the major antibiotic efflux pump (TtgABC) that exhibits an overall increased susceptibility to a wide range of drugs when compared with the wild-type strain. We used this strain as a platform to search for microbes able to produce antibiotics that inhibit growth. A collection of 2400 isolates from soil, sediments and water was generated and a drop assay developed to identify, via growth inhibition halos, strains that prevent the growth of DOT-T1E-18 on solid Luria–Bertani plates. In this study, 35 different isolates that produced known and unknown antibiotics were identified. The most potent inhibitor of DOT-T1E-18 growth was an isolate named 250J that, through multi-locus sequence analysis, was identified as a Pseudomonas sp. strain. Culture supernatants of 250J contain four different xantholysins that prevent growth of Gram-positive bacteria, Gram-negative and fungi. Two of the xantholysins were produced in higher concentrations and purified. Xantholysin A was effective against Bacillus, Lysinibacillus and Rhodococcus strains, and the effect against these microbes was enhanced when used in combination with other antibiotics such as ampicillin, gentamicin and kanamycin. Xantholysin C was also efficient against Gram-positive bacteria and showed an interesting antimicrobial effect against Pseudomonas strains, and a synergistic inhibitory effect with ampicillin, chloramphenicol and gentamicin. |
format | Online Article Text |
id | pubmed-4476826 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley & Sons, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-44768262015-07-01 Efflux pump-deficient mutants as a platform to search for microbes that produce antibiotics Molina-Santiago, Carlos Udaondo, Zulema Daddaoua, Abdelali Roca, Amalia Martín, Jesús Pérez-Victoria, Ignacio Reyes, Fernando Ramos, Juan-Luis Microb Biotechnol Research Articles Pseudomonas putida DOT-T1E-18 is a strain deficient in the major antibiotic efflux pump (TtgABC) that exhibits an overall increased susceptibility to a wide range of drugs when compared with the wild-type strain. We used this strain as a platform to search for microbes able to produce antibiotics that inhibit growth. A collection of 2400 isolates from soil, sediments and water was generated and a drop assay developed to identify, via growth inhibition halos, strains that prevent the growth of DOT-T1E-18 on solid Luria–Bertani plates. In this study, 35 different isolates that produced known and unknown antibiotics were identified. The most potent inhibitor of DOT-T1E-18 growth was an isolate named 250J that, through multi-locus sequence analysis, was identified as a Pseudomonas sp. strain. Culture supernatants of 250J contain four different xantholysins that prevent growth of Gram-positive bacteria, Gram-negative and fungi. Two of the xantholysins were produced in higher concentrations and purified. Xantholysin A was effective against Bacillus, Lysinibacillus and Rhodococcus strains, and the effect against these microbes was enhanced when used in combination with other antibiotics such as ampicillin, gentamicin and kanamycin. Xantholysin C was also efficient against Gram-positive bacteria and showed an interesting antimicrobial effect against Pseudomonas strains, and a synergistic inhibitory effect with ampicillin, chloramphenicol and gentamicin. John Wiley & Sons, Ltd 2015-07 2015-06-08 /pmc/articles/PMC4476826/ /pubmed/26059350 http://dx.doi.org/10.1111/1751-7915.12295 Text en © 2015 The Authors. Microbial Biotechnology published by John Wiley & Sons Ltd and Society for Applied Microbiology. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Molina-Santiago, Carlos Udaondo, Zulema Daddaoua, Abdelali Roca, Amalia Martín, Jesús Pérez-Victoria, Ignacio Reyes, Fernando Ramos, Juan-Luis Efflux pump-deficient mutants as a platform to search for microbes that produce antibiotics |
title | Efflux pump-deficient mutants as a platform to search for microbes that produce antibiotics |
title_full | Efflux pump-deficient mutants as a platform to search for microbes that produce antibiotics |
title_fullStr | Efflux pump-deficient mutants as a platform to search for microbes that produce antibiotics |
title_full_unstemmed | Efflux pump-deficient mutants as a platform to search for microbes that produce antibiotics |
title_short | Efflux pump-deficient mutants as a platform to search for microbes that produce antibiotics |
title_sort | efflux pump-deficient mutants as a platform to search for microbes that produce antibiotics |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4476826/ https://www.ncbi.nlm.nih.gov/pubmed/26059350 http://dx.doi.org/10.1111/1751-7915.12295 |
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