Figures & data
![Figure 1. Illustration of the double-phase solid–liquid medium preparation and plant culture. (a) 1 – cover; 2 – flask; 3 and 4 – WPMS medium with perlite at the top. (b and c) 3 and 4 – WPMS medium with perlite facing down, 5 – WPML, 6 – plantlet; and 7 – root (Patent INPI N° 105239).](/cms/asset/af903b5b-2b78-4d96-b20f-59be010b0444/tjpi_a_831489_f0001_oc.jpg)
![Figure 2. Co-culture of Pinus pinea plantlets with Pisolithus arhizus mycelium in a double-phase medium (a), negative controls: pine plantlet without fungus (b), and fungal mycelium alone (c).](/cms/asset/f0d88db1-b7c0-466e-9ef0-ad178ef3f085/tjpi_a_831489_f0002_oc.jpg)
![Figure 3. HPLC–UV chromatograms of the liquid medium sample collected from the co-culture of P. pinea plantlet inoculated with P. arhizus on day 2 (a) and liquid medium sample collected from P. pinea microshoots without fungal inoculation on day 2 (b). Peak at Rt 11.50 min corresponds to the unknown compound (UC).](/cms/asset/65a91d24-ed08-49c7-b0a2-f32874e3a010/tjpi_a_831489_f0003_oc.jpg)
![Figure 4. HPLC–UV chromatograms of samples from the co-culture of P. pinea plantlet and P. arhizus collected on day 2 spiked with IAA (a), rutin (b), and IBA (c). Peaks at Rt 11.84, 11.44, and 11.58 min correspond to the unknown compound (UC).](/cms/asset/a37186fd-8fa2-4a98-b110-907353b3f6e7/tjpi_a_831489_f0004_oc.jpg)
![Figure 5. DAD total scan (a) and total ion current (b) chromatograms of the P. pinea/P. arhizus co-culture medium samples collected at day 2. UV (a), full MS (b), and MS2 of the m/z 321 ion (c) spectra of the unknown compound (UC) in the P. pinea/P. arhizus co-culture sample collected on day 2. (b) Chemical structure of o-coumaric acid.](/cms/asset/96d2f7cd-8596-4c47-91c8-5fe0b812034e/tjpi_a_831489_f0005_oc.jpg)
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