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Biochemical pathways supporting beta-lactam biosynthesis in the springtail Folsomia candida
Recently, an active set of beta-lactam biosynthesis genes was reported in the genome of the arthropod springtail Folsomia candida (Collembola). Evidence was provided that these genes were acquired through horizontal gene transfer. However, successful integration of fungal- or bacterial-derived beta-...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5200902/ https://www.ncbi.nlm.nih.gov/pubmed/27793835 http://dx.doi.org/10.1242/bio.019620 |
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author | Suring, Wouter Mariën, Janine Broekman, Rhody van Straalen, Nico M. Roelofs, Dick |
author_facet | Suring, Wouter Mariën, Janine Broekman, Rhody van Straalen, Nico M. Roelofs, Dick |
author_sort | Suring, Wouter |
collection | PubMed |
description | Recently, an active set of beta-lactam biosynthesis genes was reported in the genome of the arthropod springtail Folsomia candida (Collembola). Evidence was provided that these genes were acquired through horizontal gene transfer. However, successful integration of fungal- or bacterial-derived beta-lactam biosynthesis into the metabolism of an animal requires the beta-lactam precursor L-α-aminoadipic acid and a phosphopantetheinyl transferase for activation of the first enzyme of the pathway, δ-(L-α-aminoadipoyl)-L-cysteinyl-D-valine synthetase (ACVS). In this study, we characterized these supporting pathways and their transcriptional regulation in F. candida. We identified one phosphopantetheinyl transferase and three pathways for L-α-aminoadipic acid production, distinct from the pathways utilized by microorganisms. We found that after heat shock, the phosphopantetheinyl transferase was co-regulated with ACVS, confirming its role in activating ACVS. Two of the three L-α-aminoadipic acid production pathways were downregulated, while PIPOX, an enzyme participating in the pipecolate pathway, was slightly co-regulated with ACVS. This indicates that L-α-aminoadipic acid may not be a limiting factor in beta-lactam biosynthesis in F. candida, in contrast to microorganisms. In conclusion, we show that all components for L-α-aminoadipic acid synthesis are present and transcriptionally active in F. candida. This demonstrates how springtails could have recruited native enzymes to integrate a beta-lactam biosynthesis pathway into their metabolism after horizontal gene transfer. |
format | Online Article Text |
id | pubmed-5200902 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-52009022017-01-13 Biochemical pathways supporting beta-lactam biosynthesis in the springtail Folsomia candida Suring, Wouter Mariën, Janine Broekman, Rhody van Straalen, Nico M. Roelofs, Dick Biol Open Research Article Recently, an active set of beta-lactam biosynthesis genes was reported in the genome of the arthropod springtail Folsomia candida (Collembola). Evidence was provided that these genes were acquired through horizontal gene transfer. However, successful integration of fungal- or bacterial-derived beta-lactam biosynthesis into the metabolism of an animal requires the beta-lactam precursor L-α-aminoadipic acid and a phosphopantetheinyl transferase for activation of the first enzyme of the pathway, δ-(L-α-aminoadipoyl)-L-cysteinyl-D-valine synthetase (ACVS). In this study, we characterized these supporting pathways and their transcriptional regulation in F. candida. We identified one phosphopantetheinyl transferase and three pathways for L-α-aminoadipic acid production, distinct from the pathways utilized by microorganisms. We found that after heat shock, the phosphopantetheinyl transferase was co-regulated with ACVS, confirming its role in activating ACVS. Two of the three L-α-aminoadipic acid production pathways were downregulated, while PIPOX, an enzyme participating in the pipecolate pathway, was slightly co-regulated with ACVS. This indicates that L-α-aminoadipic acid may not be a limiting factor in beta-lactam biosynthesis in F. candida, in contrast to microorganisms. In conclusion, we show that all components for L-α-aminoadipic acid synthesis are present and transcriptionally active in F. candida. This demonstrates how springtails could have recruited native enzymes to integrate a beta-lactam biosynthesis pathway into their metabolism after horizontal gene transfer. The Company of Biologists Ltd 2016-10-28 /pmc/articles/PMC5200902/ /pubmed/27793835 http://dx.doi.org/10.1242/bio.019620 Text en © 2016. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Suring, Wouter Mariën, Janine Broekman, Rhody van Straalen, Nico M. Roelofs, Dick Biochemical pathways supporting beta-lactam biosynthesis in the springtail Folsomia candida |
title | Biochemical pathways supporting beta-lactam biosynthesis in the springtail Folsomia candida |
title_full | Biochemical pathways supporting beta-lactam biosynthesis in the springtail Folsomia candida |
title_fullStr | Biochemical pathways supporting beta-lactam biosynthesis in the springtail Folsomia candida |
title_full_unstemmed | Biochemical pathways supporting beta-lactam biosynthesis in the springtail Folsomia candida |
title_short | Biochemical pathways supporting beta-lactam biosynthesis in the springtail Folsomia candida |
title_sort | biochemical pathways supporting beta-lactam biosynthesis in the springtail folsomia candida |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5200902/ https://www.ncbi.nlm.nih.gov/pubmed/27793835 http://dx.doi.org/10.1242/bio.019620 |
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