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Plant hairy root cultures as plasmodium modulators of the slime mold emergent computing substrate Physarum polycephalum

Roots of the medicinal plant Valeriana officinalis are well-studied for their various biological activities. We applied genetically transformed V. officinalis root biomass to exert control of Physarum polycephalum, an amoeba-based emergent computing substrate. The plasmodial stage of the P. polyceph...

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Autores principales: Ricigliano, Vincent, Chitaman, Javed, Tong, Jingjing, Adamatzky, Andrew, Howarth, Dianella G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4504241/
https://www.ncbi.nlm.nih.gov/pubmed/26236301
http://dx.doi.org/10.3389/fmicb.2015.00720
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author Ricigliano, Vincent
Chitaman, Javed
Tong, Jingjing
Adamatzky, Andrew
Howarth, Dianella G.
author_facet Ricigliano, Vincent
Chitaman, Javed
Tong, Jingjing
Adamatzky, Andrew
Howarth, Dianella G.
author_sort Ricigliano, Vincent
collection PubMed
description Roots of the medicinal plant Valeriana officinalis are well-studied for their various biological activities. We applied genetically transformed V. officinalis root biomass to exert control of Physarum polycephalum, an amoeba-based emergent computing substrate. The plasmodial stage of the P. polycephalum life cycle constitutes a single, multinucleate cell visible by unaided eye. The plasmodium modifies its network of oscillating protoplasm in response to spatial configurations of attractants and repellents, a behavior that is interpreted as biological computation. To program the computing behavior of P. polycephalum, a diverse and sustainable library of plasmodium modulators is required. Hairy roots produced by genetic transformation with Agrobacterium rhizogenes are a metabolically stable source of bioactive compounds. Adventitious roots were induced on in vitro V. officinalis plants following infection with A. rhizogenes. A single hairy root clone was selected for massive propagation and the biomass was characterized in P. polycephalum chemotaxis, maze-solving, and electrical activity assays. The Agrobacterium-derived roots of V. officinalis elicited a positive chemotactic response and augmented maze-solving behavior. In a simple plasmodium circuit, introduction of hairy root biomass stimulated the oscillation patterns of slime mold's surface electrical activity. We propose that manipulation of P. polycephalum with the plant root culture platform can be applied to the development of slime mold microfluidic devices as well as future models for engineering the plant rhizosphere.
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spelling pubmed-45042412015-07-31 Plant hairy root cultures as plasmodium modulators of the slime mold emergent computing substrate Physarum polycephalum Ricigliano, Vincent Chitaman, Javed Tong, Jingjing Adamatzky, Andrew Howarth, Dianella G. Front Microbiol Microbiology Roots of the medicinal plant Valeriana officinalis are well-studied for their various biological activities. We applied genetically transformed V. officinalis root biomass to exert control of Physarum polycephalum, an amoeba-based emergent computing substrate. The plasmodial stage of the P. polycephalum life cycle constitutes a single, multinucleate cell visible by unaided eye. The plasmodium modifies its network of oscillating protoplasm in response to spatial configurations of attractants and repellents, a behavior that is interpreted as biological computation. To program the computing behavior of P. polycephalum, a diverse and sustainable library of plasmodium modulators is required. Hairy roots produced by genetic transformation with Agrobacterium rhizogenes are a metabolically stable source of bioactive compounds. Adventitious roots were induced on in vitro V. officinalis plants following infection with A. rhizogenes. A single hairy root clone was selected for massive propagation and the biomass was characterized in P. polycephalum chemotaxis, maze-solving, and electrical activity assays. The Agrobacterium-derived roots of V. officinalis elicited a positive chemotactic response and augmented maze-solving behavior. In a simple plasmodium circuit, introduction of hairy root biomass stimulated the oscillation patterns of slime mold's surface electrical activity. We propose that manipulation of P. polycephalum with the plant root culture platform can be applied to the development of slime mold microfluidic devices as well as future models for engineering the plant rhizosphere. Frontiers Media S.A. 2015-07-16 /pmc/articles/PMC4504241/ /pubmed/26236301 http://dx.doi.org/10.3389/fmicb.2015.00720 Text en Copyright © 2015 Ricigliano, Chitaman, Tong, Adamatzky and Howarth. 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
Ricigliano, Vincent
Chitaman, Javed
Tong, Jingjing
Adamatzky, Andrew
Howarth, Dianella G.
Plant hairy root cultures as plasmodium modulators of the slime mold emergent computing substrate Physarum polycephalum
title Plant hairy root cultures as plasmodium modulators of the slime mold emergent computing substrate Physarum polycephalum
title_full Plant hairy root cultures as plasmodium modulators of the slime mold emergent computing substrate Physarum polycephalum
title_fullStr Plant hairy root cultures as plasmodium modulators of the slime mold emergent computing substrate Physarum polycephalum
title_full_unstemmed Plant hairy root cultures as plasmodium modulators of the slime mold emergent computing substrate Physarum polycephalum
title_short Plant hairy root cultures as plasmodium modulators of the slime mold emergent computing substrate Physarum polycephalum
title_sort plant hairy root cultures as plasmodium modulators of the slime mold emergent computing substrate physarum polycephalum
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4504241/
https://www.ncbi.nlm.nih.gov/pubmed/26236301
http://dx.doi.org/10.3389/fmicb.2015.00720
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