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For the quantifcation of targeted plant hormones and related compounds,
20-mg (fresh weight) portions of separately harvested roots and shoots were
weighed into 2-mL plastic microtubes (Eppendorf) and frozen in liquid nitrogen. To minimize the risk of false-positive detections, possible background
levels of analytes were subtracted from measured sample values. Therefore,
in the blank controls, 1 mL of extraction buffer containing a mixture of stable
isotopically labeled IS also was purifed. Before extraction, three 3-mm ceriastabilized zirconium oxide beads (Next Advance) were added to each sample. A mixture of stable, isotopically labeled IS was added to validate the
method and enable the precise quantifcation of endogenous levels of targetedcompounds. The amounts of IS ranged from 0.4 to 50 pmol per sample (precise amounts are listed in Supplemental Table S3). Frozen plant material was
extracted in 1 mL of ice-cold 50% aqueous (v/v) ACN using an MM 301vibration mill (Retsch) operating at a frequency of 27 Hz for 5 min. Samples were
then sonicated for 3 min at 4¡ãC using a Transsonic T310 ultrasonicator with an
ice block-flled bathtub (Elma) and subsequently extracted using a Stuart SB3
benchtop laboratory rotator (Bibby Scientifc) for 30 min at 4¡ãC. After centrifugation (10 min, 36,670 g, and 4¡ãC; Beckman Avanti 30), the supernatant was
transferred to clean plastic microtubes. Samples were further purifed according to the scheme shown in Figure 1D.

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