Materials and Reagents

Spatula–smooth narrow tip and smooth glass rod
Plastic Petri dishes (60 x 15 mm) (Corning, catalog number: 351007 )
Plastic container with wet Kimwipes inside for humidity
Paper towel or Kimwipe
Immature pea pods (1.5-2.0 cm in length) grown in sand and clay pots at 65-70 F under greenhouse conditions and freshly harvested (use within 3 h of applying a treatment). Remove calyx and retain briefly in sterile water (Figure 1). Endocarp will be used for the assay (see Note 1 in detail)
Glass vials 30 ml
Candidate elicitor solutions best dissolved in deionized water (For exceptions see Procedure 1)
DMSO
Hexane
95% ethanol

Equipment

Adjustable pipettes (P-200 and P-1000 and corresponding tips)
Flask 500 ml with 5 ml dispenser top or 5 ml pipet for dispensing hexane
Glass beakers, 30 ml
Room temperature dark cabinet space for pathogen or elicitor treatments (as described in step 3b)
UV spectrometer (Shimadzu, model: UV160 )
1 cm Pathlength quartz cuvettes (Sigma-Aldrich, catalog number: C5178 )
Note: This product has been discontinued.

Procedure

Preparation of elicitors
The selection of elicitors is by design open to innovation. Follow the directions of manufactures for solubility procedures. Water soluble compounds dissolved at near neutral pH are preferred. When solubility depends on ethanol, DMSO etc., there must be suitable control applications with only the respective solvent. Incompatible pathogen can be a positive control for an inducer of nonhost resistance. See Note 2 in detail.
Preparation of pod halves
1. Harvest pods and remove calyx as shown in Figure 1. Hold these pods in a sterile deionized water reservoir to keep the tissue moist.
2. Select uniform sized and conditioned pea pods from their water reservoir.
3. Separate the pod halves with a smooth spatula avoiding wounding as much as possible.
4. Fresh weight of pod halves is determined.
5. Lay endocarp (inner) surface layer up in a Petri dish (Figure 1).
  
  Figure 1. Pea endocarp. The inside layer (endocarp) of an immature pea pod is cuticle-free tissue capable of responding rapidly to microbes or elicitor compounds. Right picture shows endocarp tissues treated in an elicitor solution in Petri dishes. Incubation is performed in a plastic container with wet paper towels to maintain humidity.
Application of elicitors
1. Apply 25 µl of elicitor candidate solution and lightly distribute over the entire surface with a glass rod. For the control, apply the same solvent used for dissolving the elicitor.
2. Treated pods are retained in a plastic container with wet paper towels (Figure 1) to maintain humidity and then incubate in the dark or moderate light for up to 24 h.
Extraction and measurement of pisatin
1. Pods are transferred to 30 ml glass vials using forceps and immersed in 5 ml of hexane for 4 h in the dark. Typically, 400 mg fresh weight per 5 ml of hexane.
2. The hexane is decanted off into 30 ml beakers and the hexane evaporated in the air stream of a hood in low light because pisatin is not stable in bright light (typically light strength in the lab is not incandescent).
3. One milliliter of 95% ethanol is added to the residue and read at 309 nm in a cuvette using spectrophotometer.
4. To insure purity, a UV spectrum is measured in the range of 220-320 nm to verify the characteristic pisatin spectrum (Figure 2). See Note 3 in detail.
  
  Figure 2. Pisatin spectrum. UV spectrum in the range of 220-320 nm was run to verify the purity of pisatin.

Data analysis

After subtracting the OD₃₀₉ value of non-treated control, the numbers are converted based on the equation: 1.0 OD₃₀₉ unit = 43.8 µg/ml pisatin in 1 cm pathlength (see Note 4 in detail). Data should be shown with pisatin quantity (µg) per fresh weight of tissues (g). Data obtained should be analyzed using ANOVA followed by Student’s t-test. Difference with P < 0.05 is considered significant.

Notes

The pea endocarp tissue has some potential to condition or partially take up small percentages of insoluble materials in suspension, such as the cell wall fragments released by fungal spores, detected in electron microscope view (Hadwiger et al., 1981).
Effect of elicitors can be compared with that of an incompatible fungal pathogen, e.g., Fusarium solani f.sp. phaseoli (Fsph), which is a pathogen for bean (not for pea). An example result was shown in Figure 3, in which the data show that no detectable pisatin above background in water-treated tissue, and accumulation of pisatin induced by a fungal wall carbohydrate (i.e., chitosan) and by an authentic inducer of nonhost resistance in pea, a fungal pathogen of bean (i.e., Fsph).
Pisatin has been purified from the final step with both thin layer chromatography and mass spectrometry (Teasdale et al., 1974; Seneviratne et al., 2015). The assay is accurate because pisatin only absorbs at 309 nm.
Pisatin in ethanol has a characteristic UV absorption spectrum with two peaks at 286 nm and 309 nm (Figure 2). When pisatin is the only light-absorbing compound in the solution, the ratio OD₃₀₉ to OD₂₈₆ is 1.47 (Cruickshank and Perrin, 1961).

Figure 3. An example result of pisatin measurement. Pisatin was extracted and measured from endocarps (n = 3) after 24 h incubation with water (control), 1 mg/ml chitosan (elicitor), or 4 x 10⁶ spores of Fsph (Fusarium solani f.sp. phaseoli). Data was modified from our previous publication (Hartney et al., 2006). There were statistically significant differences between group means as determined by one-way ANOVA (P < 0.05).

Acknowledgments

This work was partly supported by Biologically-Intensive Agriculture and Organic Farming (BIOAg) grant from the Center for Sustaining Agriculture and Natural Resources (CSANR) at Washington State University. PPNS No. 0740, Department of Plant Pathology, College of Agricultural, Human, and Natural Resource Sciences, Agricultural Research Center, Hatch Project No. WNP01844, Washington State University, Pullman, 99164-6430, USA.

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