2002
DOI: 10.1016/s1049-9644(02)00044-0
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Pyrrolnitrin production by Burkholderia cepacia and biocontrol of Rhizoctonia stem rot of poinsettia

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Cited by 69 publications
(36 citation statements)
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“…These results are also in agreement with the earlier studies on extracellular enzyme production (Fridlender et al 1993;McKevitt et al 1989;Ogawa et al 2002). Different strains of Bcc have been reported as the source of a large variety of antifungal compounds, such as cepacin (Parker et al 1984), pyrrolnitrin (Hwang et al 2002), and siderophores (Sokol et al 1992). In our recent research, the higher level of antifungal activity was found in extraction of filter-sterilized culture supernatants of strain JK-SH007 grown in NB medium with ethyl acetate.…”
Section: Discussionsupporting
confidence: 91%
“…These results are also in agreement with the earlier studies on extracellular enzyme production (Fridlender et al 1993;McKevitt et al 1989;Ogawa et al 2002). Different strains of Bcc have been reported as the source of a large variety of antifungal compounds, such as cepacin (Parker et al 1984), pyrrolnitrin (Hwang et al 2002), and siderophores (Sokol et al 1992). In our recent research, the higher level of antifungal activity was found in extraction of filter-sterilized culture supernatants of strain JK-SH007 grown in NB medium with ethyl acetate.…”
Section: Discussionsupporting
confidence: 91%
“…Besides fluorescent pseudomonads, for which Phl þ strains have already been studied in Morens (for example, Stutz et al, 1986;Ramette et al, 2003;Frapolli et al, 2008), it is the case for the Burkholderia spp., for which certain strains produce various antifungal compounds and can antagonize fungal phytopathogens (Hwang et al, 2002;Compant et al, 2008). It applies also to taxa for which biocontrol ability has been less studied, noticeably Azospirillum spp.…”
Section: Discussionmentioning
confidence: 99%
“…Some PGPR decrease or combat the adverse effects of pathogenic microorganisms, by colonizing plants in high population during pathogen attack (Nihorimbere et al 2011). These PGPR are capable of producing antagonistic metabolites such as antibiotics (Compant et al 2005;Haas and Défago 2005), siderophores (RodrÍgueza and Fragaa 1999), HCN (Ahmad et al 2008), phenazines (Pierson and Pierson 2010), pyoluteorin (NowakThompson et al 1999), pyrrolnitrin (Hwang et al 2002). Furthermore, the PGPR must be able to deliver the chemical constituents in right amount, time, and place to effectively combat the adverse effects of pathogenic attack (Lugtenberg and Kamilova 2009).…”
Section: Introductionmentioning
confidence: 99%