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Description
  • Strigolactones are new plant hormones that induce germination of parasitic weed seeds, inhibit shoot branching, and are branching factors for AM fungi. Structureactivity relationships provide insight into their mode of action and give a model substrate for designing new active analogs.Strigolactones (SLs) constitute a new class of plant hormones which are active as germination stimulants for seeds of parasitic weeds of Striga, Orobanche, and Pelipanchi spp, in hyphal branching of arbuscular mycorrhizal (AM) fungi and as inhibitors of shoot branching. In this review, the focus is on molecular features of these SLs. The occurrence of SLs in root exudates of host plants is described. The naming protocol for SL according to the International Union of Pure and Applied Chemistry (IUPAC) rules and the oat a glance' method is explained. The total synthesis of some natural SLs is described with details for all eight stereoisomers of strigol. The problems encountered with assigning the correct structure of natural SLs are analyzed for orobanchol, alectrol, and solanacol. The structureactivity relationship of SLs as germination stimulants leads to the identification of the bioactiphore of SLs. Together with a tentative mechanism for the mode of action, a model has been derived that can be used to design and prepare active SL analogs. This working model has been used for the preparation of a series of new SL analogs such as Nijmegen-1, and analogs derived from simple ketones, keto enols, and saccharine. The serendipitous finding of SL mimics which are derived from the D-ring in SLs (appropriately substituted butenolides) is reported. For SL mimics, a mode of action is proposed as well. Recent new results support this proposal. The stability of SLs and SL analogs towards hydrolysis is described and some details of the mechanism of hydrolysis are discussed as well.
  • Strigolactones are new plant hormones that induce germination of parasitic weed seeds, inhibit shoot branching, and are branching factors for AM fungi. Structureactivity relationships provide insight into their mode of action and give a model substrate for designing new active analogs.Strigolactones (SLs) constitute a new class of plant hormones which are active as germination stimulants for seeds of parasitic weeds of Striga, Orobanche, and Pelipanchi spp, in hyphal branching of arbuscular mycorrhizal (AM) fungi and as inhibitors of shoot branching. In this review, the focus is on molecular features of these SLs. The occurrence of SLs in root exudates of host plants is described. The naming protocol for SL according to the International Union of Pure and Applied Chemistry (IUPAC) rules and the oat a glance' method is explained. The total synthesis of some natural SLs is described with details for all eight stereoisomers of strigol. The problems encountered with assigning the correct structure of natural SLs are analyzed for orobanchol, alectrol, and solanacol. The structureactivity relationship of SLs as germination stimulants leads to the identification of the bioactiphore of SLs. Together with a tentative mechanism for the mode of action, a model has been derived that can be used to design and prepare active SL analogs. This working model has been used for the preparation of a series of new SL analogs such as Nijmegen-1, and analogs derived from simple ketones, keto enols, and saccharine. The serendipitous finding of SL mimics which are derived from the D-ring in SLs (appropriately substituted butenolides) is reported. For SL mimics, a mode of action is proposed as well. Recent new results support this proposal. The stability of SLs and SL analogs towards hydrolysis is described and some details of the mechanism of hydrolysis are discussed as well. (en)
Title
  • Structure and Activity of Strigolactones: New Plant Hormones with a Rich Future
  • Structure and Activity of Strigolactones: New Plant Hormones with a Rich Future (en)
skos:prefLabel
  • Structure and Activity of Strigolactones: New Plant Hormones with a Rich Future
  • Structure and Activity of Strigolactones: New Plant Hormones with a Rich Future (en)
skos:notation
  • RIV/61989592:15310/13:33148311!RIV14-MSM-15310___
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(ED0007/01/01)
http://linked.open...iv/cisloPeriodika
  • 1
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 108376
http://linked.open...ai/riv/idVysledku
  • RIV/61989592:15310/13:33148311
http://linked.open...riv/jazykVysledku
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  • structure-activity relationship; strigolactones; plant hormones; inhibition shoot branching; hyphal branching AM fungi; germination stimulant (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • GB - Spojené království Velké Británie a Severního Irska
http://linked.open...ontrolniKodProRIV
  • [79E7A5B03980]
http://linked.open...i/riv/nazevZdroje
  • Molecular Plant
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...vavai/riv/projekt
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 6
http://linked.open...iv/tvurceVysledku
  • Pospíšil, Tomáš
  • Zwanenburg, Binne
http://linked.open...ain/vavai/riv/wos
  • 000314117100009
issn
  • 1674-2052
number of pages
http://bibframe.org/vocab/doi
  • 10.1093/mp/sss141
http://localhost/t...ganizacniJednotka
  • 15310
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