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Symbiosis extended: exchange of photosynthetic O(2) and fungal-respired CO(2) mutually power metabolism of lichen symbionts

Lichens are a symbiosis between a fungus and one or more photosynthetic microorganisms that enables the symbionts to thrive in places and conditions they could not compete independently. Exchanges of water and sugars between the symbionts are the established mechanisms that support lichen symbiosis....

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Autores principales: ten Veldhuis, Marie-Claire, Ananyev, Gennady, Dismukes, G. Charles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7052035/
https://www.ncbi.nlm.nih.gov/pubmed/31893333
http://dx.doi.org/10.1007/s11120-019-00702-0
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author ten Veldhuis, Marie-Claire
Ananyev, Gennady
Dismukes, G. Charles
author_facet ten Veldhuis, Marie-Claire
Ananyev, Gennady
Dismukes, G. Charles
author_sort ten Veldhuis, Marie-Claire
collection PubMed
description Lichens are a symbiosis between a fungus and one or more photosynthetic microorganisms that enables the symbionts to thrive in places and conditions they could not compete independently. Exchanges of water and sugars between the symbionts are the established mechanisms that support lichen symbiosis. Herein, we present a new linkage between algal photosynthesis and fungal respiration in lichen Flavoparmelia caperata that extends the physiological nature of symbiotic co-dependent metabolisms, mutually boosting energy conversion rates in both symbionts. Measurements of electron transport by oximetry show that photosynthetic O(2) is consumed internally by fungal respiration. At low light intensity, very low levels of O(2) are released, while photosynthetic electron transport from water oxidation is normal as shown by intrinsic chlorophyll variable fluorescence yield (period-4 oscillations in flash-induced Fv/Fm). The rate of algal O(2) production increases following consecutive series of illumination periods, at low and with limited saturation at high light intensities, in contrast to light saturation in free-living algae. We attribute this effect to arise from the availability of more CO(2) produced by fungal respiration of photosynthetically generated sugars. We conclude that the lichen symbionts are metabolically coupled by energy conversion through exchange of terminal electron donors and acceptors used in both photosynthesis and fungal respiration. Algal sugars and O(2) are consumed by the fungal symbiont, while fungal delivered CO(2) is consumed by the alga. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11120-019-00702-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-70520352020-03-16 Symbiosis extended: exchange of photosynthetic O(2) and fungal-respired CO(2) mutually power metabolism of lichen symbionts ten Veldhuis, Marie-Claire Ananyev, Gennady Dismukes, G. Charles Photosynth Res Original Article Lichens are a symbiosis between a fungus and one or more photosynthetic microorganisms that enables the symbionts to thrive in places and conditions they could not compete independently. Exchanges of water and sugars between the symbionts are the established mechanisms that support lichen symbiosis. Herein, we present a new linkage between algal photosynthesis and fungal respiration in lichen Flavoparmelia caperata that extends the physiological nature of symbiotic co-dependent metabolisms, mutually boosting energy conversion rates in both symbionts. Measurements of electron transport by oximetry show that photosynthetic O(2) is consumed internally by fungal respiration. At low light intensity, very low levels of O(2) are released, while photosynthetic electron transport from water oxidation is normal as shown by intrinsic chlorophyll variable fluorescence yield (period-4 oscillations in flash-induced Fv/Fm). The rate of algal O(2) production increases following consecutive series of illumination periods, at low and with limited saturation at high light intensities, in contrast to light saturation in free-living algae. We attribute this effect to arise from the availability of more CO(2) produced by fungal respiration of photosynthetically generated sugars. We conclude that the lichen symbionts are metabolically coupled by energy conversion through exchange of terminal electron donors and acceptors used in both photosynthesis and fungal respiration. Algal sugars and O(2) are consumed by the fungal symbiont, while fungal delivered CO(2) is consumed by the alga. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11120-019-00702-0) contains supplementary material, which is available to authorized users. Springer Netherlands 2019-12-31 2020 /pmc/articles/PMC7052035/ /pubmed/31893333 http://dx.doi.org/10.1007/s11120-019-00702-0 Text en © The Author(s) 2019 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Article
ten Veldhuis, Marie-Claire
Ananyev, Gennady
Dismukes, G. Charles
Symbiosis extended: exchange of photosynthetic O(2) and fungal-respired CO(2) mutually power metabolism of lichen symbionts
title Symbiosis extended: exchange of photosynthetic O(2) and fungal-respired CO(2) mutually power metabolism of lichen symbionts
title_full Symbiosis extended: exchange of photosynthetic O(2) and fungal-respired CO(2) mutually power metabolism of lichen symbionts
title_fullStr Symbiosis extended: exchange of photosynthetic O(2) and fungal-respired CO(2) mutually power metabolism of lichen symbionts
title_full_unstemmed Symbiosis extended: exchange of photosynthetic O(2) and fungal-respired CO(2) mutually power metabolism of lichen symbionts
title_short Symbiosis extended: exchange of photosynthetic O(2) and fungal-respired CO(2) mutually power metabolism of lichen symbionts
title_sort symbiosis extended: exchange of photosynthetic o(2) and fungal-respired co(2) mutually power metabolism of lichen symbionts
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7052035/
https://www.ncbi.nlm.nih.gov/pubmed/31893333
http://dx.doi.org/10.1007/s11120-019-00702-0
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