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A sacrificial millipede altruistically protects its swarm using a drone blood enzyme, mandelonitrile oxidase
Soldiers of some eusocial insects exhibit an altruistic self-destructive defense behavior in emergency situations when attacked by large enemies. The swarm-forming invasive millipede, Chamberlinius hualienensis, which is not classified as eusocial animal, exudes irritant chemicals such as benzoyl cy...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4893617/ https://www.ncbi.nlm.nih.gov/pubmed/27265180 http://dx.doi.org/10.1038/srep26998 |
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author | Ishida, Yuko Kuwahara, Yasumasa Dadashipour, Mohammad Ina, Atsutoshi Yamaguchi, Takuya Morita, Masashi Ichiki, Yayoi Asano, Yasuhisa |
author_facet | Ishida, Yuko Kuwahara, Yasumasa Dadashipour, Mohammad Ina, Atsutoshi Yamaguchi, Takuya Morita, Masashi Ichiki, Yayoi Asano, Yasuhisa |
author_sort | Ishida, Yuko |
collection | PubMed |
description | Soldiers of some eusocial insects exhibit an altruistic self-destructive defense behavior in emergency situations when attacked by large enemies. The swarm-forming invasive millipede, Chamberlinius hualienensis, which is not classified as eusocial animal, exudes irritant chemicals such as benzoyl cyanide as a defensive secretion. Although it has been thought that this defensive chemical was converted from mandelonitrile, identification of the biocatalyst has remained unidentified for 40 years. Here, we identify the novel blood enzyme, mandelonitrile oxidase (ChuaMOX), which stoichiometrically catalyzes oxygen consumption and synthesis of benzoyl cyanide and hydrogen peroxide from mandelonitrile. Interestingly the enzymatic activity is suppressed at a blood pH of 7, and the enzyme is segregated by membranes of defensive sacs from mandelonitrile which has a pH of 4.6, the optimum pH for ChuaMOX activity. In addition, strong body muscle contractions are necessary for de novo synthesis of benzoyl cyanide. We propose that, to protect its swarm, the sacrificial millipede also applies a self-destructive defense strategy—the endogenous rupturing of the defensive sacs to mix ChuaMOX and mandelonitrile at an optimum pH. Further study of defensive systems in primitive arthropods will pave the way to elucidate the evolution of altruistic defenses in the animal kingdom. |
format | Online Article Text |
id | pubmed-4893617 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48936172016-06-10 A sacrificial millipede altruistically protects its swarm using a drone blood enzyme, mandelonitrile oxidase Ishida, Yuko Kuwahara, Yasumasa Dadashipour, Mohammad Ina, Atsutoshi Yamaguchi, Takuya Morita, Masashi Ichiki, Yayoi Asano, Yasuhisa Sci Rep Article Soldiers of some eusocial insects exhibit an altruistic self-destructive defense behavior in emergency situations when attacked by large enemies. The swarm-forming invasive millipede, Chamberlinius hualienensis, which is not classified as eusocial animal, exudes irritant chemicals such as benzoyl cyanide as a defensive secretion. Although it has been thought that this defensive chemical was converted from mandelonitrile, identification of the biocatalyst has remained unidentified for 40 years. Here, we identify the novel blood enzyme, mandelonitrile oxidase (ChuaMOX), which stoichiometrically catalyzes oxygen consumption and synthesis of benzoyl cyanide and hydrogen peroxide from mandelonitrile. Interestingly the enzymatic activity is suppressed at a blood pH of 7, and the enzyme is segregated by membranes of defensive sacs from mandelonitrile which has a pH of 4.6, the optimum pH for ChuaMOX activity. In addition, strong body muscle contractions are necessary for de novo synthesis of benzoyl cyanide. We propose that, to protect its swarm, the sacrificial millipede also applies a self-destructive defense strategy—the endogenous rupturing of the defensive sacs to mix ChuaMOX and mandelonitrile at an optimum pH. Further study of defensive systems in primitive arthropods will pave the way to elucidate the evolution of altruistic defenses in the animal kingdom. Nature Publishing Group 2016-06-06 /pmc/articles/PMC4893617/ /pubmed/27265180 http://dx.doi.org/10.1038/srep26998 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Ishida, Yuko Kuwahara, Yasumasa Dadashipour, Mohammad Ina, Atsutoshi Yamaguchi, Takuya Morita, Masashi Ichiki, Yayoi Asano, Yasuhisa A sacrificial millipede altruistically protects its swarm using a drone blood enzyme, mandelonitrile oxidase |
title | A sacrificial millipede altruistically protects its swarm using a drone blood enzyme, mandelonitrile oxidase |
title_full | A sacrificial millipede altruistically protects its swarm using a drone blood enzyme, mandelonitrile oxidase |
title_fullStr | A sacrificial millipede altruistically protects its swarm using a drone blood enzyme, mandelonitrile oxidase |
title_full_unstemmed | A sacrificial millipede altruistically protects its swarm using a drone blood enzyme, mandelonitrile oxidase |
title_short | A sacrificial millipede altruistically protects its swarm using a drone blood enzyme, mandelonitrile oxidase |
title_sort | sacrificial millipede altruistically protects its swarm using a drone blood enzyme, mandelonitrile oxidase |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4893617/ https://www.ncbi.nlm.nih.gov/pubmed/27265180 http://dx.doi.org/10.1038/srep26998 |
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