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Phytate Degradation by Fungi and Bacteria that Inhabit Sawdust and Coffee Residue Composts

Phytate is the primary source of organic phosphorus, but it cannot be directly utilized by plants and is strongly adsorbed by the soil, reducing bioavailability. Composting is a process used to improve the bioavailability of phytate in organic wastes through degradation by microorganisms. In this st...

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Autores principales: Eida, Mohamed Fathallh, Nagaoka, Toshinori, Wasaki, Jun, Kouno, Kenji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese Society of Microbial Ecology/The Japanese Society of Soil Microbiology 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4070677/
https://www.ncbi.nlm.nih.gov/pubmed/23100024
http://dx.doi.org/10.1264/jsme2.ME12083
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author Eida, Mohamed Fathallh
Nagaoka, Toshinori
Wasaki, Jun
Kouno, Kenji
author_facet Eida, Mohamed Fathallh
Nagaoka, Toshinori
Wasaki, Jun
Kouno, Kenji
author_sort Eida, Mohamed Fathallh
collection PubMed
description Phytate is the primary source of organic phosphorus, but it cannot be directly utilized by plants and is strongly adsorbed by the soil, reducing bioavailability. Composting is a process used to improve the bioavailability of phytate in organic wastes through degradation by microorganisms. In this study, we aimed to investigate the phytate-degrading ability of fungi and bacteria that inhabit sawdust compost and coffee residue compost, and their contribution to the composting process. In the plate assay, the fungi that formed clear zones around their colonies belonged to the genera Mucor, Penicillium, Galactomyces, Coniochaeta, Aspergillus, and Fusarium, while the bacteria belonged to the genera Pseudomonas, Enterobacter, Chitinophaga, and Rahnella. Eight fungal isolates (genera Mucor, Penicillium, Galactomyces, and Coniochaeta) and four bacterial isolates (genera Pseudomonas, Enterobacter, and Rahnella) were selected to evaluate phytase activity in their liquid culture and their ability to degrade phytate in organic materials composed of mushroom media residue and rice bran. The selected fungi degraded phytate in organic materials to varying degrees. Penicillium isolates showed the highest degradation ability and Coniochaeta isolate exhibited relatively high degradation ability. The clear zone diameters of these fungal isolates displayed significantly positive and negative correlations with inorganic and phytate phosphorus contents in the organic materials after incubation, respectively; however, none of the selected bacteria reduced phytate phosphorus in organic materials. It is therefore possible that fungi are major contributors to phytate degradation during composting.
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spelling pubmed-40706772014-07-24 Phytate Degradation by Fungi and Bacteria that Inhabit Sawdust and Coffee Residue Composts Eida, Mohamed Fathallh Nagaoka, Toshinori Wasaki, Jun Kouno, Kenji Microbes Environ Articles Phytate is the primary source of organic phosphorus, but it cannot be directly utilized by plants and is strongly adsorbed by the soil, reducing bioavailability. Composting is a process used to improve the bioavailability of phytate in organic wastes through degradation by microorganisms. In this study, we aimed to investigate the phytate-degrading ability of fungi and bacteria that inhabit sawdust compost and coffee residue compost, and their contribution to the composting process. In the plate assay, the fungi that formed clear zones around their colonies belonged to the genera Mucor, Penicillium, Galactomyces, Coniochaeta, Aspergillus, and Fusarium, while the bacteria belonged to the genera Pseudomonas, Enterobacter, Chitinophaga, and Rahnella. Eight fungal isolates (genera Mucor, Penicillium, Galactomyces, and Coniochaeta) and four bacterial isolates (genera Pseudomonas, Enterobacter, and Rahnella) were selected to evaluate phytase activity in their liquid culture and their ability to degrade phytate in organic materials composed of mushroom media residue and rice bran. The selected fungi degraded phytate in organic materials to varying degrees. Penicillium isolates showed the highest degradation ability and Coniochaeta isolate exhibited relatively high degradation ability. The clear zone diameters of these fungal isolates displayed significantly positive and negative correlations with inorganic and phytate phosphorus contents in the organic materials after incubation, respectively; however, none of the selected bacteria reduced phytate phosphorus in organic materials. It is therefore possible that fungi are major contributors to phytate degradation during composting. Japanese Society of Microbial Ecology/The Japanese Society of Soil Microbiology 2013-03 2012-10-26 /pmc/articles/PMC4070677/ /pubmed/23100024 http://dx.doi.org/10.1264/jsme2.ME12083 Text en Copyright © 2013 by the Japanese Society of Microbial Ecology / the Japanese Society of Soil Microbiology http://creativecommons.org/licenses/by/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Eida, Mohamed Fathallh
Nagaoka, Toshinori
Wasaki, Jun
Kouno, Kenji
Phytate Degradation by Fungi and Bacteria that Inhabit Sawdust and Coffee Residue Composts
title Phytate Degradation by Fungi and Bacteria that Inhabit Sawdust and Coffee Residue Composts
title_full Phytate Degradation by Fungi and Bacteria that Inhabit Sawdust and Coffee Residue Composts
title_fullStr Phytate Degradation by Fungi and Bacteria that Inhabit Sawdust and Coffee Residue Composts
title_full_unstemmed Phytate Degradation by Fungi and Bacteria that Inhabit Sawdust and Coffee Residue Composts
title_short Phytate Degradation by Fungi and Bacteria that Inhabit Sawdust and Coffee Residue Composts
title_sort phytate degradation by fungi and bacteria that inhabit sawdust and coffee residue composts
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4070677/
https://www.ncbi.nlm.nih.gov/pubmed/23100024
http://dx.doi.org/10.1264/jsme2.ME12083
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