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In situ stable isotope probing of phosphate-solubilizing bacteria in the hyphosphere

This study used a [(13)C]DNA stable isotope probing (SIP) technique to elucidate a direct pathway for the translocation of (13)C-labeled photoassimilate from maize plants to extraradical mycelium-associated phosphate-solubilizing bacteria (PSB) that mediate the mineralization and turnover of soil or...

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Autores principales: Wang, Fei, Shi, Ning, Jiang, Rongfeng, Zhang, Fusuo, Feng, Gu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4783358/
https://www.ncbi.nlm.nih.gov/pubmed/26802172
http://dx.doi.org/10.1093/jxb/erv561
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author Wang, Fei
Shi, Ning
Jiang, Rongfeng
Zhang, Fusuo
Feng, Gu
author_facet Wang, Fei
Shi, Ning
Jiang, Rongfeng
Zhang, Fusuo
Feng, Gu
author_sort Wang, Fei
collection PubMed
description This study used a [(13)C]DNA stable isotope probing (SIP) technique to elucidate a direct pathway for the translocation of (13)C-labeled photoassimilate from maize plants to extraradical mycelium-associated phosphate-solubilizing bacteria (PSB) that mediate the mineralization and turnover of soil organic phosphorus (P) in the hyphosphere. Inoculation with PSB alone did not provide any benefit to maize plants but utilized the added phytate-P to their own advantage, while inoculation with Rhizophagus irregularis alone significantly promoted shoot biomass and P content compared with the control. However, compared with both sole inoculation treatments, combined inoculation with PSB and R. irregularis in the hyphosphere enhanced organic P mineralization and increased microbial biomass P in the soil. There was no extra benefit to plant P uptake but the hyphal growth of R. irregularis was reduced, suggesting that PSB benefited from the arbuscular mycorrhizal (AM) fungal mycelium and competed for soil P with the fungus. The combination of T-RFLP (terminal restriction fragment length polymorphism) analysis with a clone library revealed that one of the bacteria that actively assimilated carbon derived from pulse-labeled maize plants was Pseudomonas alcaligenes (Pseudomonadaceae) that was initially inoculated into the hyphosphere soil. These results provide the first in situ demonstration of the pathway underlying the carbon flux from plants to the AM mycelium-associated PSB, and the PSB assimilated the photosynthates exuded by the fungus and promoted mineralization and turnover of organic P in the soil.
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spelling pubmed-47833582016-03-10 In situ stable isotope probing of phosphate-solubilizing bacteria in the hyphosphere Wang, Fei Shi, Ning Jiang, Rongfeng Zhang, Fusuo Feng, Gu J Exp Bot Research Paper This study used a [(13)C]DNA stable isotope probing (SIP) technique to elucidate a direct pathway for the translocation of (13)C-labeled photoassimilate from maize plants to extraradical mycelium-associated phosphate-solubilizing bacteria (PSB) that mediate the mineralization and turnover of soil organic phosphorus (P) in the hyphosphere. Inoculation with PSB alone did not provide any benefit to maize plants but utilized the added phytate-P to their own advantage, while inoculation with Rhizophagus irregularis alone significantly promoted shoot biomass and P content compared with the control. However, compared with both sole inoculation treatments, combined inoculation with PSB and R. irregularis in the hyphosphere enhanced organic P mineralization and increased microbial biomass P in the soil. There was no extra benefit to plant P uptake but the hyphal growth of R. irregularis was reduced, suggesting that PSB benefited from the arbuscular mycorrhizal (AM) fungal mycelium and competed for soil P with the fungus. The combination of T-RFLP (terminal restriction fragment length polymorphism) analysis with a clone library revealed that one of the bacteria that actively assimilated carbon derived from pulse-labeled maize plants was Pseudomonas alcaligenes (Pseudomonadaceae) that was initially inoculated into the hyphosphere soil. These results provide the first in situ demonstration of the pathway underlying the carbon flux from plants to the AM mycelium-associated PSB, and the PSB assimilated the photosynthates exuded by the fungus and promoted mineralization and turnover of organic P in the soil. Oxford University Press 2016-04 2016-01-21 /pmc/articles/PMC4783358/ /pubmed/26802172 http://dx.doi.org/10.1093/jxb/erv561 Text en © The Author 2016. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by/3.0 This 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Wang, Fei
Shi, Ning
Jiang, Rongfeng
Zhang, Fusuo
Feng, Gu
In situ stable isotope probing of phosphate-solubilizing bacteria in the hyphosphere
title In situ stable isotope probing of phosphate-solubilizing bacteria in the hyphosphere
title_full In situ stable isotope probing of phosphate-solubilizing bacteria in the hyphosphere
title_fullStr In situ stable isotope probing of phosphate-solubilizing bacteria in the hyphosphere
title_full_unstemmed In situ stable isotope probing of phosphate-solubilizing bacteria in the hyphosphere
title_short In situ stable isotope probing of phosphate-solubilizing bacteria in the hyphosphere
title_sort in situ stable isotope probing of phosphate-solubilizing bacteria in the hyphosphere
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4783358/
https://www.ncbi.nlm.nih.gov/pubmed/26802172
http://dx.doi.org/10.1093/jxb/erv561
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