Probing strigolactone perception mechanisms with rationally designed small-molecule agonists stimulating germination of root parasitic weeds
The development of potent strigolactone (SL) agonists as suicidal germination inducers could be a useful strategy for controlling root parasitic weeds, but uncertainty about the SL perception mechanism impedes real progress. Here we describe small-molecule agonists that efficiently stimulate Phelipa...
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Veröffentlicht in: | Nature communications 2022-07, Vol.13 (1), p.3987-3987, Article 3987 |
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Sprache: | eng |
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Zusammenfassung: | The development of potent strigolactone (SL) agonists as suicidal germination inducers could be a useful strategy for controlling root parasitic weeds, but uncertainty about the SL perception mechanism impedes real progress. Here we describe small-molecule agonists that efficiently stimulate
Phelipanchce aegyptiaca
, and
Striga hermonthica
, germination in concentrations as low as 10
−8
to 10
−17
M. We show that full efficiency of synthetic SL agonists in triggering signaling through the
Striga
SL receptor, ShHTL7, depends on the receptor-catalyzed hydrolytic reaction of the agonists. Additionally, we reveal that the stereochemistry of synthetic SL analogs affects the hydrolytic ability of ShHTL7 by influencing the probability of the privileged conformations of ShHTL7. Importantly, an alternative ShHTL7-mediated hydrolysis mechanism, proceeding via nucleophilic attack of the NE2 atom of H246 to the 2′C of the D-ring, is reported. Together, our findings provide insight into SL hydrolysis and structure-perception mechanisms, and potent suicide germination stimulants, which would contribute to the elimination of the noxious parasitic weeds.
Strigolactone agonists could potentially help control noxious weeds by promoting suicidal germination. Here the authors describe a series of small molecule agonists that stimulate germination via the
Striga
ShHTL7 receptor and show that stereochemistry and hydrolysis-independent signalling mediate potency. |
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ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/s41467-022-31710-9 |