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Insights into phosphatase-activated chemical defense in a marine sponge holobiont
Marine sponges often contain potent cytotoxic compounds, which in turn evokes the principle question of how marine sponges avoid self-toxicity. In a marine sponge Discodermia calyx, the highly toxic calyculin A is detoxified by the phosphorylation, which is catalyzed by the phosphotransferase CalQ o...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
RSC
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8637855/ https://www.ncbi.nlm.nih.gov/pubmed/34977575 http://dx.doi.org/10.1039/d1cb00163a |
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author | Jomori, Takahiro Matsuda, Kenichi Egami, Yoko Abe, Ikuro Takai, Akira Wakimoto, Toshiyuki |
author_facet | Jomori, Takahiro Matsuda, Kenichi Egami, Yoko Abe, Ikuro Takai, Akira Wakimoto, Toshiyuki |
author_sort | Jomori, Takahiro |
collection | PubMed |
description | Marine sponges often contain potent cytotoxic compounds, which in turn evokes the principle question of how marine sponges avoid self-toxicity. In a marine sponge Discodermia calyx, the highly toxic calyculin A is detoxified by the phosphorylation, which is catalyzed by the phosphotransferase CalQ of a producer symbiont, “Candidatus Entotheonella” sp. Here we show the activating mechanism to dephosphorylate the stored phosphocalyculin A protoxin. The phosphatase specific to phosphocalyculin A is CalL, which is also encoded in the calyculin biosynthetic gene cluster. CalL represents a new clade and unprecedently coordinates the heteronuclear metals Cu and Zn. CalL is localized in the periplasmic space of the sponge symbiont, where it is ready for the on-demand production of calyculin A in response to sponge tissue disruption. |
format | Online Article Text |
id | pubmed-8637855 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | RSC |
record_format | MEDLINE/PubMed |
spelling | pubmed-86378552021-12-30 Insights into phosphatase-activated chemical defense in a marine sponge holobiont Jomori, Takahiro Matsuda, Kenichi Egami, Yoko Abe, Ikuro Takai, Akira Wakimoto, Toshiyuki RSC Chem Biol Chemistry Marine sponges often contain potent cytotoxic compounds, which in turn evokes the principle question of how marine sponges avoid self-toxicity. In a marine sponge Discodermia calyx, the highly toxic calyculin A is detoxified by the phosphorylation, which is catalyzed by the phosphotransferase CalQ of a producer symbiont, “Candidatus Entotheonella” sp. Here we show the activating mechanism to dephosphorylate the stored phosphocalyculin A protoxin. The phosphatase specific to phosphocalyculin A is CalL, which is also encoded in the calyculin biosynthetic gene cluster. CalL represents a new clade and unprecedently coordinates the heteronuclear metals Cu and Zn. CalL is localized in the periplasmic space of the sponge symbiont, where it is ready for the on-demand production of calyculin A in response to sponge tissue disruption. RSC 2021-10-06 /pmc/articles/PMC8637855/ /pubmed/34977575 http://dx.doi.org/10.1039/d1cb00163a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Jomori, Takahiro Matsuda, Kenichi Egami, Yoko Abe, Ikuro Takai, Akira Wakimoto, Toshiyuki Insights into phosphatase-activated chemical defense in a marine sponge holobiont |
title | Insights into phosphatase-activated chemical defense in a marine sponge holobiont |
title_full | Insights into phosphatase-activated chemical defense in a marine sponge holobiont |
title_fullStr | Insights into phosphatase-activated chemical defense in a marine sponge holobiont |
title_full_unstemmed | Insights into phosphatase-activated chemical defense in a marine sponge holobiont |
title_short | Insights into phosphatase-activated chemical defense in a marine sponge holobiont |
title_sort | insights into phosphatase-activated chemical defense in a marine sponge holobiont |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8637855/ https://www.ncbi.nlm.nih.gov/pubmed/34977575 http://dx.doi.org/10.1039/d1cb00163a |
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