Collection of Xylem Exudates from the Model Plant Arabidopsis and the Crop Plant Soybean

Materials and Reagents

1. 1.5 mL tube (BIO-BIK, catalog number: ST-0150F)

2. Plastic square dish (140 mm × 100 mm, height 18 mm/EIKEN, catalog number: AW2000)

3. Plastic Petri dish (ø 85 mm, height 20 mm/EIKEN, catalog number: AP2310)

4. Razor blade (FEATHER, FA-10)

5. Micropipette [Nichiryo, catalog number: 00-NPX2-2 (0.1–2 µL)]

6. Arabidopsis seeds

7. Ethanol (FUJIFILM Wako, catalog number: 057-00451)

8. Tween 20 (MP Biomedicals, catalog number: 194841)

9. Sodium hypochlorite solution (FUJIFILM Wako, catalog number: 197-02206)

10. Murashige and Skoog (MS) plant salt mixture (FUJIFILM Wako, catalog number: 392-00591)

11. Gamborg’s vitamin solution 1,000× (Sigma-Aldrich, catalog number: G1019)

12. Sucrose (FUJIFILM Wako, catalog number: 196-00015)

13. Agar (FUJIFILM Wako, catalog number: 016-11875)

14. Culture media (100 mL) (see Recipes)

Equipment

1. Growth chamber (Nippon Medical & Chemical Instruments, model: LH-241S)

Procedure

1. Place Arabidopsis seeds in 1.5 mL tubes.

2. Add 1 mL of 70% ethanol and wash the seeds for 1 min.

3. Remove the ethanol solution.

4. Add 1 mL of H₂O, 10 µL of 10% Tween 20, and 50 µL of sodium hypochlorite solution and mix using a vortex mixer.

5. Wash the seeds for 15 min by gently inverting the tubes.

6. Remove the solution and rinse the seeds five times with sterilized water.

7. Sow the seeds in plastic Petri dishes with culture media (see Recipes).

8. Incubate at 4 °C for three days.

9. Cover the dishes with aluminum foil to grow seedlings in darkness and incubate at 23 °C for five days.

10. Remove the aluminum foil. At this stage, the seedlings are etiolated with elongated hypocotyls (Figure 1A). Note that further darkness affects seedling viability.

11. Grow the seedlings under a 10 h light/14 h dark cycle at 23 °C for five days. The cotyledons will become green (Figure 1B).

12. Transfer the Arabidopsis seedlings to plastic square dishes with culture media [with or without 1% sucrose (see Notes 1)] on a clean bench.

13. Place the dishes vertically and incubate the plants under a 10 h light [100 µmol/m²s photosynthetic photon flux density (PPFD)]/14 h dark cycle at 23 °C for 14 days (Figure 1C).

14. Cut the hypocotyls with a razor blade (Figure 1D). Within 20–40 min, xylem exudates will form droplets on the cut surface of the cotyledon (Figure 1E).

15. Wipe the first droplets with soft paper to avoid contamination of phloem sap and then collect the droplets with a micropipette. The droplets can be sampled at approximately 30 min intervals.

16. Store the collected exudates at -80 °C.

    
    

    
    Figure 1. Collection of xylem exudates from Arabidopsis. (A) Arabidopsis seedlings at five days after germination (DAG), grown under dark conditions. (B) Arabidopsis seedlings at 10 DAG, incubated under a light/dark cycle for five days. (C) Arabidopsis plants at 24 DAG. (D) Arabidopsis hypocotyls are cut with a razor blade. (E) and (F) Xylem exudates form droplets on the cut surface of hypocotyls, and these droplets are collected with a micropipette. Each droplet is indicated by a triangle.

Notes

1. In our study (Okamoto et al., 2022a), because the target peptide gene responds to low-carbon conditions, Arabidopsis was cultured without sucrose from 10–24 DAG. The exudate was collected for 4 h, and approximately 320 µL of exudate was obtained from 360 plants. Application of sucrose to the culture medium increases the yield of xylem exudates.

2. The amount of xylem exudates obtained from Arabidopsis is too small to conduct proteomics analysis (approximately 1 µL/plant), so the purpose of analyzing Arabidopsis xylem exudate should be the detection of interesting (target) molecule(s).

3. To conduct a comprehensive analysis, a larger amount of xylem exudates must be collected from larger plants (see Part II).

Recipes

1. Culture media (100 mL)

   Reagent	Final concentration	Amount
   Murashige and Skoog (MS) salt mixture	1/2×	0.23 g
   Sucrose	1 or 0% (w/v)	1 or 0 g
   Gamborg’s vitamin solution 1,000×	1×	100 µL

   Adjust the pH to 5.7 and add 0.8 g agar; then, autoclave the solution for 20 min at 121 °C.

   
   

Part II. Collection of xylem exudates from soybean

Materials and Reagents

1. Soybean seeds

2. 50 mL centrifuge tubes (Labcon, catalog number: 3181-345)

3. Plastic square dish (140 mm × 100 mm, height 18 mm/EIKEN, catalog number: AW2000)

4. Silicon tube [select a tube whose inner diameter is fitted to or slightly larger than (less than 1 mm larger) the cut stems. In the case of soybean, the diameter of the lower internodes is 4–7 mm approximately seven weeks after germination. The length of the tube depends on the length of the flat needle or micropipette tip. When the flat needle described below was used, we cut the tube into approximately 8 cm lengths [AsOne, catalog number: 6-586-12 (4 mm i.d.), 6-586-17 (5 mm i.d.), 6-586-20 (6 mm i.d.), and 6-586-25 (7 mm i.d.)]

5. Plastic pot (ø 150 mm, height 127 mm)

6. Garden shears

7. Flat needle (AsOne, catalog number: 1-2752-01)

8. 5 mL syringe (TERUMO, catalog number: SS-05SZ)

9. Ethanol (FUJIFILM Wako, catalog number: 057-00451)

10. Vermiculite

11. Clay

12. Nutrition solution for soybean (1 L) (see Recipes)

Equipment

1. Greenhouse or growth chamber (Nippon Medical & Chemical Instruments, model: LH-411PFQDT-SP)

2. Centrifuge (Kubota, model: 2410)

Procedure

1. Place seeds (less than 25 mL to facilitate washes) in 50 mL centrifuge tubes and add approximately 40 mL of 70% ethanol to wash the seeds by inverting gently for 1 min.

2. Rinse the seeds with distilled water five times.

3. Place soft wet paper on plastic square dishes and arrange the seeds on the paper (approximately 25 seeds/dish) (Figure 2A).

4. Cover the seeds with wet, soft paper and place a lid on the dishes to maintain higher humidity (Figure 2B).

5. Incubate the seeds in the square dishes under a 16 h light (200 µmol/m²s PPFD)/8 h dark cycle at 23 °C for two days.

6. Select healthy seedlings (e.g., relatively long roots, greening cotyledon) and transplant them into vermiculite in plastic pots.

7. Place the pots in a growth chamber [16 h light (900 µmol/m²s PPFD)/8 h dark, 23 °C, and humidity not controlled] or greenhouse and supply a sufficient amount of nutrition solution. The frequency of solution application depends on the plant age, conditions, and weather (in the case of a greenhouse).

8. Approximately seven weeks after germination, cut the hypocotyls or lower internodes (first or second internodes from hypocotyls) with garden shears (Figure 2C, D). The hypocotyls and the lower internodes are too hard to cut with a razor blade.

9. Wash the cut surface with distilled water by dripping water on the surface.

10. Allow the cut stem to leak exudates for 20 min to avoid contamination from phloem sap.

11. Wipe the cut surface and the side of the stem with soft paper and wrap the stem just beneath the cut surface with clay (make a clay ring around the stem) (Figure 2E). Note that the droplets on the side of the stem prevent clay from sticking to the stem; therefore, the droplets need to be completely wiped off.

12. Place and press a silicon tube into the clay to avoid leakage of xylem exudates (Figure 2F). The gap between the stem and tube should be sealed with clay.

13. Collect xylem exudates using a syringe with a flat needle or micropipette. The exudates can be sampled at 20–30 min intervals.

14. Clay particles sometimes contaminate the exudates. To remove them from the xylem exudates, centrifuge at 2,600 × g for 10 min (and optimally at 4 °C) and transfer the supernatant to a new tube.

15. Store the xylem exudates at -80 °C.

    
    

    
    Figure 2. Collection of xylem exudates from soybean. (A) Soybean seeds were arranged on soft wet paper in a plastic square dish. (B) The seeds were covered with wet paper, and a lid was placed on the dishes. (C) Lower internodes (1^st or 2^nd internodes from the bottom) of soybean. The plants were grown in a growth chamber (PPFD = 900 µmol/m²s). (D) Hypocotyl or lower internodes were cut with garden shears. (E) The stem just beneath the cut surface was wrapped with clay. (F) A silicon tube is pressed onto the cut stem, and xylem exudates accumulate in the tube. (G) From cutting the internodes to the fitting of a tube (C–F), it takes less than 1 min per plant, so this method is applicable to collecting xylem exudates from a large number of plants for comprehensive analysis.

Notes

1. A larger quantity of exudates will be obtained when plants are cultured in a greenhouse rather than in a growth chamber.

2. Under greenhouse conditions, approximately 60 mL of xylem exudate was obtained from 12 soybean plants (45 DAG) during the five hours after cutting the stems (approximately 5 mL/plant).

3. The yield of xylem exudates can decrease under stressed conditions, such as low-N and salt stress conditions. In our case, when soybean plants were cultured under a low-N (1.2 mM NH₄NO₃) condition for the last five days, approximately 20 mL of xylem exudate was obtained from 11 soybean plants in five hours. When soybean plants were cultured with the nutrition solution containing 50 mM NaCl for the last five days, no xylem exudates were obtained.

4. This method can be applied to various dicot plants. Under greenhouse conditions, approximately 120 mL of xylem exudate was obtained from 14 tomato (Solanum lycopersicum) plants (45 DAG) during the five hours after cutting the stems (approximately 8.6 mL/plant), and seven endogenous peptides were identified (Okamoto et al., 2022b).

Recipes

1. Nutrition solution for soybean (1 L)

   Reagent	Final concentration	Amount
   NH4NO3	6.0 mM	480 mg
   CaCl2·2H2O	1.8 mM	262 mg
   MgSO4·7H2O	1.0 mM	245 mg
   KH2PO4	0.8 mM	108.8 mg
   K2SO4	0.28 mM	49.6 mg
   Fe(III)-EDTA	0.1 mM	43.9 mg
   MnSO4·5H2O	5.9 µM	1.43 mg
   H3BO3	4.0 µM	0.25 mg
   CuSO4·5H2O	1.0 µM	0.25 mg
   ZnSO4·7H2O	0.87 µM	0.25 mg
   Na2MoO4·2H2O	0.21 µM	0.05 mg
   CoCl2·6H2O	0.13 µM	0.03 mg

   The reagents are dissolved in desalted water, and total volume is adjusted to 1 L.

   The pH is adjusted to 6.0.

Acknowledgments

These procedures are based on Okamoto et al. (2022a) and Okamoto et al. (2015). This work was supported by JST PRESTO (JPMJPR17Q2 to S.O.) and the MEXT Leading Initiative for Excellent Young Researchers (to S.O.).

Competing interests

The authors declare no competing interests.

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