Journal
PHYTOCHEMISTRY
Volume 137, Issue -, Pages 123-131Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.phytochem.2017.02.010
Keywords
Maize (Zea mays); Strigolactones; Zealactone; Striga hermonthica (Orobanchaceae); Seed germination; UHPLC-MS-MS; Prep-HPLC-MS; NMR
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In the root exudate and root extracts of maize hybrid cv NK Falkone seven putative strigolactones were detected using UPLC-TQ-MS-MS. All seven compounds displayed MS-MS-fragmentation common for strigolactones and particularly the presence of a fragment of m/z 97 Da, which may indicate the presence of the so-called D-ring, suggests they are strigolactones. The levels of all these putative strigolactones increased upon phosphate starvation and decreased upon fluridone (carotenoid biosynthesis inhibitor) treatment, both of which are a common response for strigolactones. All seven compounds were subsequently isolated with prep-HPLC-MS. They all exhibited Srriga hermonthica seed germination inducing activity just as the synthetic strigolactone analog CR24. The structure of two of the seven compounds was elucidated by NMR spectroscopy as: methyl (2E,3E)-4-(3,3-dimethyl-5-oxo-2-(prop-1-en-2-yl)tetrahydrofuran-2-yl)-2-(((4-methyl-5-oxo-2,5-dihydrofuran-2-yl)oxy)methylene)but-3-enoate (two diastereomers 1a and 2b). Strigolactones (1a/b) are closely related to the methyl ester of carlactonoic acid (MeCLA) and heliolactone. However, they contain a unique 4,4-dimethyltetrahydrofuran-2-one motif as the A-ring instead of the classical (di)methylcyclohexene. Because these compounds were isolated from maize (Zea mays) we called them zealactone la and lb. The implications of this discovery for our view on strigolactones and their biosynthesis are discussed. (C) 2017 Elsevier Ltd. All rights reserved.
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