Structure elucidation of a compound overaccumulating in tt4 seeds. A, Differential analysis of wild-type and tt4 LC/ESI(+)-QTOF-MS profiles revealed altered features at m/z 386.183, 387.188, 388.189, and 165.058 coeluting at 7.0 min. These features belong to a single compound mass spectrum due to their chromatogram correlation and are annotated as molecular ion (m/z 386), isotope (m/z 387 and 388), and in-source fragment (m/z 165). Calculation of elemental composition (constraints: 1H, 12C, 16O without limitation, 14N ≤ 5, 32S ≤ 2, even electron state, DBE ≥ −2) yields 10 potential sum formulas for the molecular ion within 15 ppm error. B, The molecular ion is detected by direct infusion ESI(+)-FTICR-MS in fraction I of a tt4 seed extract at m/z 386.18029. Determination of elemental composition applying the same constraints results in a single sum formula within 2 ppm error. C, The molecular ion is collisionally fragmented at different collision energies (15 and 25 eV) by QTOF-MS. Elemental compositions were calculated for each fragment ion and each neutral loss. D, A hypothetical fragmentation scheme is constructed, and substructure information from characteristic fragment ions (m/z 121.017, 4-hydroxybenzoyl) and neutral losses (m/z 59.07 D, C3H9N; m/z 162.05 D, C6H10O5) was combined to a biologically reasonable molecular structure. To further validate the structural assignment, the aglycone of the compound was chemically synthesized. The CID mass spectrum of synthetic 4-hydroxybenzoylcholine shows fragment ions at m/z 165, 121, and 93, as observed in the CID mass spectra of the new compound.