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Utilisation of Carbon Sources by Pythium, Phytophthora and Fusarium Species as Determined by Biolog(®) Microplate Assay
This study examined the metabolic activity of pure cultures of five root pathogens commonly found in closed hydroponic cultivation systems (Phytophthora cryptogea (PC), Phytophthora capsici (PCP), Pythium aphanidermatum (PA), Fusarium oxysporum f.sp. radicis-lycopersici (FORL) and Fusarium solani (F...
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Formato: | Texto |
Lenguaje: | English |
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Bentham Open
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2656775/ https://www.ncbi.nlm.nih.gov/pubmed/19294012 http://dx.doi.org/10.2174/1874285800903010009 |
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author | Khalil, Sammar Alsanius, Beatrix W |
author_facet | Khalil, Sammar Alsanius, Beatrix W |
author_sort | Khalil, Sammar |
collection | PubMed |
description | This study examined the metabolic activity of pure cultures of five root pathogens commonly found in closed hydroponic cultivation systems (Phytophthora cryptogea (PC), Phytophthora capsici (PCP), Pythium aphanidermatum (PA), Fusarium oxysporum f.sp. radicis-lycopersici (FORL) and Fusarium solani (FS)) using sole carbon source utilisation in order to develop effective biocontrol strategies against these pathogens. Aliquots of 150 µL of the mycelial suspension were inoculated in each well of GN2 microtitre plates. On the basis of average well colour development and number of positive wells, the pathogens were divided into two groups, (i) PA and FORL and (ii) PC, PCP and FS. Group (i) was characterised by a short lag-phase, a rapid exponential phase involving almost all carbon sources offered and a long stationary phase, while group (ii) had a more extended lag-phase and a slower utilisation rate of the carbon sources offered. The three isolates in group (ii) differed significantly during their exponential phase. The lowest utilisation rate of carbon sources and number of sources utilised was found for PCP. Of the major group of carbon sources, six carbohydrates, three carboxylic acids and four amino acids were rapidly used by all isolates tested at an early stage. The carbon sources gentibiose, α-D-glucose, maltose, sucrose, D-trehalose, L-aspartic acid, L-glutamic acid, L-proline persisted to the end of the exponential phase.Moreover, similarities between the metabolic profiles of the tested pathogen and the those of the resident microflora could also be found. These findings are of great importance as regards the role of the resident microflora in the biocontrol. |
format | Text |
id | pubmed-2656775 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Bentham Open |
record_format | MEDLINE/PubMed |
spelling | pubmed-26567752009-03-17 Utilisation of Carbon Sources by Pythium, Phytophthora and Fusarium Species as Determined by Biolog(®) Microplate Assay Khalil, Sammar Alsanius, Beatrix W Open Microbiol J Article This study examined the metabolic activity of pure cultures of five root pathogens commonly found in closed hydroponic cultivation systems (Phytophthora cryptogea (PC), Phytophthora capsici (PCP), Pythium aphanidermatum (PA), Fusarium oxysporum f.sp. radicis-lycopersici (FORL) and Fusarium solani (FS)) using sole carbon source utilisation in order to develop effective biocontrol strategies against these pathogens. Aliquots of 150 µL of the mycelial suspension were inoculated in each well of GN2 microtitre plates. On the basis of average well colour development and number of positive wells, the pathogens were divided into two groups, (i) PA and FORL and (ii) PC, PCP and FS. Group (i) was characterised by a short lag-phase, a rapid exponential phase involving almost all carbon sources offered and a long stationary phase, while group (ii) had a more extended lag-phase and a slower utilisation rate of the carbon sources offered. The three isolates in group (ii) differed significantly during their exponential phase. The lowest utilisation rate of carbon sources and number of sources utilised was found for PCP. Of the major group of carbon sources, six carbohydrates, three carboxylic acids and four amino acids were rapidly used by all isolates tested at an early stage. The carbon sources gentibiose, α-D-glucose, maltose, sucrose, D-trehalose, L-aspartic acid, L-glutamic acid, L-proline persisted to the end of the exponential phase.Moreover, similarities between the metabolic profiles of the tested pathogen and the those of the resident microflora could also be found. These findings are of great importance as regards the role of the resident microflora in the biocontrol. Bentham Open 2009-01-15 /pmc/articles/PMC2656775/ /pubmed/19294012 http://dx.doi.org/10.2174/1874285800903010009 Text en © Khalil and Alsanius; Licensee Bentham Open. http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited. |
spellingShingle | Article Khalil, Sammar Alsanius, Beatrix W Utilisation of Carbon Sources by Pythium, Phytophthora and Fusarium Species as Determined by Biolog(®) Microplate Assay |
title | Utilisation of Carbon Sources by Pythium, Phytophthora and Fusarium Species as Determined by Biolog(®) Microplate Assay |
title_full | Utilisation of Carbon Sources by Pythium, Phytophthora and Fusarium Species as Determined by Biolog(®) Microplate Assay |
title_fullStr | Utilisation of Carbon Sources by Pythium, Phytophthora and Fusarium Species as Determined by Biolog(®) Microplate Assay |
title_full_unstemmed | Utilisation of Carbon Sources by Pythium, Phytophthora and Fusarium Species as Determined by Biolog(®) Microplate Assay |
title_short | Utilisation of Carbon Sources by Pythium, Phytophthora and Fusarium Species as Determined by Biolog(®) Microplate Assay |
title_sort | utilisation of carbon sources by pythium, phytophthora and fusarium species as determined by biolog(®) microplate assay |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2656775/ https://www.ncbi.nlm.nih.gov/pubmed/19294012 http://dx.doi.org/10.2174/1874285800903010009 |
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