Abstract

Strigolactones (SLs), a novel class of plant hormones, are key regulator of plant architecture and mediator of biotic interactions in the rhizosphere. Root-released SLs initiate the establishment of arbuscular mycorrhizal (AM) symbiosis by inducing spore germination and hyphal branching in AM fungi (AMF). However, these compounds also trigger the germination of root parasitic weeds, paving the way for deleterious infestation. Availability of SLs is required for investigating of their functions and also for application in agriculture. However, natural SLs are difficult to synthesize due to their complex structure and cannot be isolated at large scale, as they are released at very low concentrations. Therefore, there is a need for synthetic SL analogs. Recently, we reported on the development of simple SL analogs, methyl phenlactonoates (MPs), which show high SL activity in plants. Here, we investigate the effect of MP1, MP3 and the widely used SL-analog GR24 on AMF spore germination and host root colonization. Our results show that MP1 and MP3 inhibit AMF spore germination, but promote the intra-radical root colonization, both more efficiently than GR24. These results indicate that field application of MP1 and MP3 does not have negative impact on mycorrhizal fungi. In conclusion, our data together with the previously reported simple synthesis, high activity in regulating plant architecture and inducing Striga seed germination, demonstrate the utility of MP1 and MP3 as for field application in combating root parasitic weeds by inducing germination in host's absence.

Highlights

  • Strigolactones (SLs) are a class of plant hormones and signaling molecules with a wide spectrum of activities

  • Root-released SLs initiate the establishment of arbuscular mycorrhizal (AM) symbiosis by inducing spore germination and hyphal branching in AM fungi (AMF)

  • We examined the effect of MP1 and MP3 on the

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Summary

Introduction

Strigolactones (SLs) are a class of plant hormones and signaling molecules with a wide spectrum of activities. The synthesis of SLs is initiated by the b-carotene isomerase (Dwarf, D27) that forms 9-cis-b-carotene from the corresponding all-trans-isomer [28, 29] This is followed by a stereospecific oxidative cleavage reaction that is catalyzed by the carotenoid cleavage dioxygenase 7 (CCD7) and leads to b-ionone and a 9-cis-configured intermediate [28, 30]. Hyphal branching and/or spore germination assays are widely used to assess the activity of SL-analogs on AM fungi [9, 10] These assays only provide insights into their effects during the pre-symbiotic steps of AMF [39], which -during their life cyclethrive in two niches, the rhizosphere and the root. These findings indicate that both compounds may be used for suicidal germination to combat Striga spp without negatively impact the AM symbiotic process

Synthetic strigolactone analogs
Statistical analysis
Results
MP1 and MP3 promote mycorrhizal colonization
Discussion
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