Elucidation of Antifungal Metabolites Produced by Pseudomonas aurantiaca IB5-10 with Broad-Spectrum Antifungal Activity

Antifungal metabolites were isolated from a culture of Pseudomonas aurantiaca IBS-10. Chemical structures of the metabolites were elucidated as phenazine-1-carboxylic acid (PCA; 1), 2-hydroxyphenazine (2-OH-PHZ; 2), and cyclo-(L-Pro-L-Val; 3), respectively, based on spectroscopic methods. Among them...

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Published inJournal of microbiology and biotechnology Vol. 22; no. 3; pp. 326 - 330
Main Authors Park, G.K., Yeungnam University, Gyeongsan, Republic of Korea, Lim, J.H., Yeungnam University, Gyeongsan, Republic of Korea, Kim, S.D., Yeungnam University, Gyeongsan, Republic of Korea, Shim, S.H., Yeungnam University, Gyeongsan, Republic of Korea
Format Journal Article
LanguageEnglish
Published Seoul Korean Society for Applied Microbiology 01.03.2012
한국미생물·생명공학회
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ISSN1017-7825
1738-8872
DOI10.4014/jmb.1106.06042

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Summary:Antifungal metabolites were isolated from a culture of Pseudomonas aurantiaca IBS-10. Chemical structures of the metabolites were elucidated as phenazine-1-carboxylic acid (PCA; 1), 2-hydroxyphenazine (2-OH-PHZ; 2), and cyclo-(L-Pro-L-Val; 3), respectively, based on spectroscopic methods. Among them, 3 was isolated for the first time from this strain. The antifungal activities of 1-3 were evaluated against a variety of plant pathogens. To the best of our knowledge, the antifungal activities of 3 against plant fungal pathogens have been evaluated for the first time in this work. PCA (1) showed the most potent antifungal activities against Phytophthora capsici, Rhizoctonia solani AG-1(IA), and Pythium ultimum with MICs (㎍/ml) of less than 1.0, 1.3, and 2.0, respectively. On the other hand, 2-OH-PHZ (2) showed potent antifungal activity against R. solani AG-1(IA) with the MIC (㎍/ml) of 2.0, whereas it showed moderate antifungal activity against P. ultimum with the MIC (㎍/ml) of 50.0. In addition, 3 showed antifungal activity against only R. solani AG-1(IA).
Bibliography:2013000102
A50
G704-000169.2012.22.3.016
ISSN:1017-7825
1738-8872
DOI:10.4014/jmb.1106.06042