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Organic Chemistry (Note)

Ability of plant pathogenic fungi Gibberella fujikuroi and Fusarium commune to react with airborne methyl jasmonate

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Pages 1650-1654 | Received 11 Mar 2019, Accepted 23 Apr 2019, Published online: 15 May 2019

Figures & data

Figure 1. Biosynthetic pathway of jasmonic acid (octadecanoid pathway).

Figure 1. Biosynthetic pathway of jasmonic acid (octadecanoid pathway).

Figure 2. Evaluation of (+)-cis-OPDA, JA-Ile, and JA in G. fujikuroi. The fungus was treated with airborne MeJA-d5. The endogenous amounts of (+)-cis-OPDA, JA-Ile and JA were analyzed by UPLC-MS/MS with MRM in negative mode. (a) The presence of (+)-cis-OPDA. Upper panel: The peak derived from [17,17,18,18,18-2H5] (+)-cis-OPDA (internal standard) was monitored by selecting m/z 296.37 as the pseudomolecular ion and m/z 170.99 as the transition ion. Lower panel: The peak derived from (+)-cis-OPDA (endogenous compound) was monitored by selecting m/z 291.37 as the pseudomolecular ion and m/z 164.99 as the transition ion; (b) The evaluation of endogenous amounts of (+)-cis-OPDA; (c) The evaluation of endogenous amounts of JA-Ile; (d) The evaluation of endogenous amounts of JA; (e) The presence of [2,2,5,5,7-2H5] JA derived from deuterium-labeled MeJA. Upper panel: The peak derived from [2,2,5,5,7-2H5] JA was monitored by selecting m/z 214.00 as the pseudomolecular ion and m/z 60.71 as the transition ion. Lower panel: The peak derived from JA (endogenous compound) was monitored by selecting m/z 209.00 as the pseudomolecular ion and m/z 58.71 as the transition ion. Each value is represented by the mean ± SD of five independent replicates. Welch’s test, **p< 0.01, *p< 0.05. x) originated from the acetone extract (100 mL).

Figure 2. Evaluation of (+)-cis-OPDA, JA-Ile, and JA in G. fujikuroi. The fungus was treated with airborne MeJA-d5. The endogenous amounts of (+)-cis-OPDA, JA-Ile and JA were analyzed by UPLC-MS/MS with MRM in negative mode. (a) The presence of (+)-cis-OPDA. Upper panel: The peak derived from [17,17,18,18,18-2H5] (+)-cis-OPDA (internal standard) was monitored by selecting m/z 296.37 as the pseudomolecular ion and m/z 170.99 as the transition ion. Lower panel: The peak derived from (+)-cis-OPDA (endogenous compound) was monitored by selecting m/z 291.37 as the pseudomolecular ion and m/z 164.99 as the transition ion; (b) The evaluation of endogenous amounts of (+)-cis-OPDA; (c) The evaluation of endogenous amounts of JA-Ile; (d) The evaluation of endogenous amounts of JA; (e) The presence of [2,2,5,5,7-2H5] JA derived from deuterium-labeled MeJA. Upper panel: The peak derived from [2,2,5,5,7-2H5] JA was monitored by selecting m/z 214.00 as the pseudomolecular ion and m/z 60.71 as the transition ion. Lower panel: The peak derived from JA (endogenous compound) was monitored by selecting m/z 209.00 as the pseudomolecular ion and m/z 58.71 as the transition ion. Each value is represented by the mean ± SD of five independent replicates. Welch’s test, **p< 0.01, *p< 0.05. x) originated from the acetone extract (100 mL).

Figure 3. Evaluation of JA in F. commune. The fungus was treated with airborne MeJA-d5. The endogenous amounts of JA were analyzed by UPLC-MS/MS with MRM in negative mode. (a) The evaluation of endogenous amounts of JA; (b) The presence of [2,2,5,5,7-2H5] JA derived from deuterium-labeled MeJA. Upper panel: The peak derived from [2,2,5,5,7-2H5] JA was monitored by selecting m/z 214.00 as the pseudomolecular ion and m/z 60.71 as the transition ion. Lower panel: The peak derived from JA (endogenous compound) was monitored by selecting m/z 209.00 as the pseudomolecular ion and m/z 58.71 as the transition ion. Each value is represented by the mean ± SD of five independent replicates. Welch’s test, **p< 0.01, *p < 0.05. x) originated from the acetone extract (100 mL).

Figure 3. Evaluation of JA in F. commune. The fungus was treated with airborne MeJA-d5. The endogenous amounts of JA were analyzed by UPLC-MS/MS with MRM in negative mode. (a) The evaluation of endogenous amounts of JA; (b) The presence of [2,2,5,5,7-2H5] JA derived from deuterium-labeled MeJA. Upper panel: The peak derived from [2,2,5,5,7-2H5] JA was monitored by selecting m/z 214.00 as the pseudomolecular ion and m/z 60.71 as the transition ion. Lower panel: The peak derived from JA (endogenous compound) was monitored by selecting m/z 209.00 as the pseudomolecular ion and m/z 58.71 as the transition ion. Each value is represented by the mean ± SD of five independent replicates. Welch’s test, **p< 0.01, *p < 0.05. x) originated from the acetone extract (100 mL).
Supplemental material

Rishni_funji_JA_supplementfigures.pdf

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