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Identification of novel tylosin analogues generated by a wblA disruption mutant of Streptomyces ansochromogenes

BACKGROUND: Streptomyces, as the main source of antibiotics, has been intensively exploited for discovering new drug candidates to combat the evolving pathogens. Disruption of wblA, an actinobacteria-specific gene controlling major developmental transition, can cause the alteration of phenotype and...

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Autores principales: Lu, Cheng, Liao, Guojian, Zhang, Jihui, Tan, Huarong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4630966/
https://www.ncbi.nlm.nih.gov/pubmed/26525981
http://dx.doi.org/10.1186/s12934-015-0359-5
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author Lu, Cheng
Liao, Guojian
Zhang, Jihui
Tan, Huarong
author_facet Lu, Cheng
Liao, Guojian
Zhang, Jihui
Tan, Huarong
author_sort Lu, Cheng
collection PubMed
description BACKGROUND: Streptomyces, as the main source of antibiotics, has been intensively exploited for discovering new drug candidates to combat the evolving pathogens. Disruption of wblA, an actinobacteria-specific gene controlling major developmental transition, can cause the alteration of phenotype and morphology in many species of Streptomyces. One wblA homologue was found in Streptomyces ansochromogenes 7100 by using the Basic Local Alignment Search Tool. It is interesting to identify whether novel secondary metabolites could be produced by the wblA disruption mutant as evidenced in other Streptomyces. RESULTS: The wblA disruption mutant of S. ansochromogenes 7100 (ΔwblA) was constructed by homologous recombination. ΔwblA failed to produce spores and nikkomycin, the major product of S. ansochromogenes 7100 (wild-type strain) during fermentation. Antibacterial activity against Staphylococcus aureus and Bacillus cereus was observed with fermentation broth of ΔwblA but not with that of the wild-type strain. To identify the antibacterial compounds, the two compounds (compound 1 and compound 2) produced by ΔwblA were characterized as 16-membered macrolides by mass spectrometry and nuclear magnetic resonance spectroscopy. The chemical structure of these compounds shows similarity with tylosin, and the bioassays indicated that the two compounds inhibited the growth of a number of gram-positive bacteria. It is intriguing that they displayed much higher activity than tylosin against Streptococcus pneumoniae. CONCLUSIONS: Two novel tylosin analogues (compound 1 and 2) were generated by ΔwblA. Bioassays showed that compound 1 and 2 displayed much higher activity than tylosin against Streptococcus pneumoniae, implying that these two compounds might be used to widen the application of tylosin. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-015-0359-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-46309662015-11-04 Identification of novel tylosin analogues generated by a wblA disruption mutant of Streptomyces ansochromogenes Lu, Cheng Liao, Guojian Zhang, Jihui Tan, Huarong Microb Cell Fact Research BACKGROUND: Streptomyces, as the main source of antibiotics, has been intensively exploited for discovering new drug candidates to combat the evolving pathogens. Disruption of wblA, an actinobacteria-specific gene controlling major developmental transition, can cause the alteration of phenotype and morphology in many species of Streptomyces. One wblA homologue was found in Streptomyces ansochromogenes 7100 by using the Basic Local Alignment Search Tool. It is interesting to identify whether novel secondary metabolites could be produced by the wblA disruption mutant as evidenced in other Streptomyces. RESULTS: The wblA disruption mutant of S. ansochromogenes 7100 (ΔwblA) was constructed by homologous recombination. ΔwblA failed to produce spores and nikkomycin, the major product of S. ansochromogenes 7100 (wild-type strain) during fermentation. Antibacterial activity against Staphylococcus aureus and Bacillus cereus was observed with fermentation broth of ΔwblA but not with that of the wild-type strain. To identify the antibacterial compounds, the two compounds (compound 1 and compound 2) produced by ΔwblA were characterized as 16-membered macrolides by mass spectrometry and nuclear magnetic resonance spectroscopy. The chemical structure of these compounds shows similarity with tylosin, and the bioassays indicated that the two compounds inhibited the growth of a number of gram-positive bacteria. It is intriguing that they displayed much higher activity than tylosin against Streptococcus pneumoniae. CONCLUSIONS: Two novel tylosin analogues (compound 1 and 2) were generated by ΔwblA. Bioassays showed that compound 1 and 2 displayed much higher activity than tylosin against Streptococcus pneumoniae, implying that these two compounds might be used to widen the application of tylosin. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-015-0359-5) contains supplementary material, which is available to authorized users. BioMed Central 2015-11-02 /pmc/articles/PMC4630966/ /pubmed/26525981 http://dx.doi.org/10.1186/s12934-015-0359-5 Text en © Lu et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Lu, Cheng
Liao, Guojian
Zhang, Jihui
Tan, Huarong
Identification of novel tylosin analogues generated by a wblA disruption mutant of Streptomyces ansochromogenes
title Identification of novel tylosin analogues generated by a wblA disruption mutant of Streptomyces ansochromogenes
title_full Identification of novel tylosin analogues generated by a wblA disruption mutant of Streptomyces ansochromogenes
title_fullStr Identification of novel tylosin analogues generated by a wblA disruption mutant of Streptomyces ansochromogenes
title_full_unstemmed Identification of novel tylosin analogues generated by a wblA disruption mutant of Streptomyces ansochromogenes
title_short Identification of novel tylosin analogues generated by a wblA disruption mutant of Streptomyces ansochromogenes
title_sort identification of novel tylosin analogues generated by a wbla disruption mutant of streptomyces ansochromogenes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4630966/
https://www.ncbi.nlm.nih.gov/pubmed/26525981
http://dx.doi.org/10.1186/s12934-015-0359-5
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