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Characterization of Linoleate 10-Hydratase of Lactobacillus plantarum and Novel Antifungal Metabolites
Lactobacilli convert linoleic acid to the antifungal compound 10-hydroxy-12-octadecenoic acid (10-HOE) by linoleate 10-hydratase (10-LAH). However, the effect of this conversion on cellular membrane physiology and properties of the cell surface have not been demonstrated. Moreover, Lactobacillus pla...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5047880/ https://www.ncbi.nlm.nih.gov/pubmed/27757104 http://dx.doi.org/10.3389/fmicb.2016.01561 |
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author | Chen, Yuan Y. Liang, Nuan Y. Curtis, Jonathan M. Gänzle, Michael G. |
author_facet | Chen, Yuan Y. Liang, Nuan Y. Curtis, Jonathan M. Gänzle, Michael G. |
author_sort | Chen, Yuan Y. |
collection | PubMed |
description | Lactobacilli convert linoleic acid to the antifungal compound 10-hydroxy-12-octadecenoic acid (10-HOE) by linoleate 10-hydratase (10-LAH). However, the effect of this conversion on cellular membrane physiology and properties of the cell surface have not been demonstrated. Moreover, Lactobacillus plantarum produces 13-hydroxy-9-octadecenoic acid (13-HOE) in addition to 10-HOE, but the antifungal activity of 13-HOE was unknown. Phylogenetic analyses conducted in this study did not differentiate between 10-LAH and linoleate 13-hydratase (13-LAH). Thus, linoleate hydratases (LAHs) must be characterized through their differences in their activities of linoleate conversion. Four genes encoding putative LAHs from lactobacilli were cloned, heterologous expressed, purified and identified as FAD-dependent 10-LAH. The unsaturated fatty acid substrates stimulated the growth of lactobacilli. We also investigated the role of 10-LAH in ethanol tolerance, membrane fluidity and hydrophobicity of cell surfaces in lactobacilli by disruption of lah. Compared with the L. plantarum lah deficient strain, 10-LAH in wild-type strain did not exert effect on cell survival and membrane fluidity under ethanol stress, but influenced the cell surface hydrophobicity. Moreover, deletion of 10-LAH in L. plantarum facilitated purification of 13-HOE and demonstration of its antifungal activity against Penicillium roqueforti and Aspergillus niger. |
format | Online Article Text |
id | pubmed-5047880 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50478802016-10-18 Characterization of Linoleate 10-Hydratase of Lactobacillus plantarum and Novel Antifungal Metabolites Chen, Yuan Y. Liang, Nuan Y. Curtis, Jonathan M. Gänzle, Michael G. Front Microbiol Microbiology Lactobacilli convert linoleic acid to the antifungal compound 10-hydroxy-12-octadecenoic acid (10-HOE) by linoleate 10-hydratase (10-LAH). However, the effect of this conversion on cellular membrane physiology and properties of the cell surface have not been demonstrated. Moreover, Lactobacillus plantarum produces 13-hydroxy-9-octadecenoic acid (13-HOE) in addition to 10-HOE, but the antifungal activity of 13-HOE was unknown. Phylogenetic analyses conducted in this study did not differentiate between 10-LAH and linoleate 13-hydratase (13-LAH). Thus, linoleate hydratases (LAHs) must be characterized through their differences in their activities of linoleate conversion. Four genes encoding putative LAHs from lactobacilli were cloned, heterologous expressed, purified and identified as FAD-dependent 10-LAH. The unsaturated fatty acid substrates stimulated the growth of lactobacilli. We also investigated the role of 10-LAH in ethanol tolerance, membrane fluidity and hydrophobicity of cell surfaces in lactobacilli by disruption of lah. Compared with the L. plantarum lah deficient strain, 10-LAH in wild-type strain did not exert effect on cell survival and membrane fluidity under ethanol stress, but influenced the cell surface hydrophobicity. Moreover, deletion of 10-LAH in L. plantarum facilitated purification of 13-HOE and demonstration of its antifungal activity against Penicillium roqueforti and Aspergillus niger. Frontiers Media S.A. 2016-10-04 /pmc/articles/PMC5047880/ /pubmed/27757104 http://dx.doi.org/10.3389/fmicb.2016.01561 Text en Copyright © 2016 Chen, Liang, Curtis and Gänzle. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Chen, Yuan Y. Liang, Nuan Y. Curtis, Jonathan M. Gänzle, Michael G. Characterization of Linoleate 10-Hydratase of Lactobacillus plantarum and Novel Antifungal Metabolites |
title | Characterization of Linoleate 10-Hydratase of Lactobacillus plantarum and Novel Antifungal Metabolites |
title_full | Characterization of Linoleate 10-Hydratase of Lactobacillus plantarum and Novel Antifungal Metabolites |
title_fullStr | Characterization of Linoleate 10-Hydratase of Lactobacillus plantarum and Novel Antifungal Metabolites |
title_full_unstemmed | Characterization of Linoleate 10-Hydratase of Lactobacillus plantarum and Novel Antifungal Metabolites |
title_short | Characterization of Linoleate 10-Hydratase of Lactobacillus plantarum and Novel Antifungal Metabolites |
title_sort | characterization of linoleate 10-hydratase of lactobacillus plantarum and novel antifungal metabolites |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5047880/ https://www.ncbi.nlm.nih.gov/pubmed/27757104 http://dx.doi.org/10.3389/fmicb.2016.01561 |
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