Background: Plant chemical defense can be elicited by signaling chemicals. As yet, the elicitation is mainly known from volatile aboveground signals. Root-secreted belowground signals and their underlying mechanisms are largely unknown. This study examined a root-secreted signaling (-)-loliolide to trigger chemical defense in rice and wheat against pests by means of cocultivation and incubation experiments.
Results: Wild-type Arabidopsis (WT) and its root exudates with (-)-loliolide induced the production of defensive metabolites of rice and wheat and reduced the performance of weeds, pathogens and herbivores, while a carotenoid-deficient mutant (szl1-1) and its root exudates without (-)-loliolide had no similar effects. However, the induction and reduction occurred in the szl1-1 root exudates by (-)-loliolide supplementation with the level equal to that of WT. RNA-sequencing analysis revealed a significant change in the transcript level of defense-related genes in rice exposure to (-)-loliolide. Furthermore, (-)-loliolide enhanced rice resistance against Rhizoctonia solani through changing reactive oxygen species (ROS) system, and mediating jasmonic acid, salicylic acid and abscisic acid biosynthesis.
Conclusion: Root-secreted signaling (-)-loliolide can trigger chemical defense in rice and wheat against their pests. Such perception-dependent chemical defenses provide an intriguing possibility for ecological pest management to increase crop productivity and sustainability. © 2024 Society of Chemical Industry.
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http://dx.doi.org/10.1002/ps.8378 | DOI Listing |
Pest Manag Sci
January 2025
College of Plant Science and Technology, Huazhong Agricultural University, Wuhan, China.
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January 2025
Institute of Virology and Biotechnology, State Key Laboratory for Managing Biotic and Chemical Treats to the Quality and Safety of Agro-Products, Key Laboratory of Biotechnology in Plant Protection of Zhejiang Province, Zhejiang Academy of Agricultural Sciences, Hangzhou 310021, P. R. China.
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January 2025
Research School of Chemistry, Australian National University, Canberra, Australian Capital Territory, Australia.
Drug targeting strategies, such as peptide-drug conjugates (PDCs), have arisen to combat the issue of off-target toxicity that is commonly associated with chemotherapeutic small molecule drugs. Here we investigated the ability of PDCs comprising a human protein-derived cell-penetrating peptide-platelet factor 4-derived internalization peptide (PDIP)-as a targeting strategy to improve the selectivity of camptothecin (CPT), a topoisomerase I inhibitor that suffers from off-target toxicity. The intranuclear target of CPT allowed exploration of PDC design features required for optimal potency.
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January 2025
Department of Mechanical Science and Engineering, The Grainger College of Engineering, University of Illinois Urbana-Champaign, Urbana, IL, USA.
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January 2025
Department of Chemical and Biological Engineering, Northwestern University, Evanston, IL, USA.
Enzyme engineering is limited by the challenge of rapidly generating and using large datasets of sequence-function relationships for predictive design. To address this challenge, we develop a machine learning (ML)-guided platform that integrates cell-free DNA assembly, cell-free gene expression, and functional assays to rapidly map fitness landscapes across protein sequence space and optimize enzymes for multiple, distinct chemical reactions. We apply this platform to engineer amide synthetases by evaluating substrate preference for 1217 enzyme variants in 10,953 unique reactions.
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