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Discrimination of Oviposition Deterrent Volatile ?-Ionone by Odorant-Binding Proteins 1 and 4 in the Whitefly Bemisia tabaci.


ABSTRACT: : The whitefly, Bemisia tabaci, is an important invasive economic pest of agricultural crops worldwide. ?-ionone has a significant oviposition repellent effect against B. tabaci, but the olfactory molecular mechanism of this insect for recognizing ?-ionone is unclear. To clarify the binding properties of odorant-binding proteins (OBPs) with ?-ionone, we performed gene cloning, evolution analysis, bacterial expression, fluorescence competitive binding assay, and molecular docking to study the binding function of OBP1 and OBP4 on ?-ionone. The results showed that after the OBP1 and OBP4 proteins were recombined, the compound ?-ionone exhibited a reduction in the fluorescence binding affinity to <50%, with a dissociation constant of 5.15 and 3.62 ?M for OBP1 and OBP4, respectively. Our data indicate that ?-ionone has high affinity for OBP1 and OBP4, which play a crucial role in the identification of oviposition sites in B. tabaci. The findings of this study suggest that whiteflies employ ?-ionone compound in the selection of the suitable egg-laying sites on host plants during the oviposition behavior.

SUBMITTER: Li F 

PROVIDER: S-EPMC6843521 | biostudies-literature | 2019 Oct

REPOSITORIES: biostudies-literature

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Discrimination of Oviposition Deterrent Volatile β-Ionone by Odorant-Binding Proteins 1 and 4 in the Whitefly <i>Bemisia tabaci</i>.

Li Fengqi F   Li Du D   Dewer Youssef Y   Qu Cheng C   Yang Zhen Z   Tian Jiahui J   Luo Chen C  

Biomolecules 20191003 10


<b>:</b> The whitefly, <i>Bemisia</i><i>tabaci</i>, is an important invasive economic pest of agricultural crops worldwide. β-ionone has a significant oviposition repellent effect against <i>B.</i><i>tabaci</i>, but the olfactory molecular mechanism of this insect for recognizing β-ionone is unclear. To clarify the binding properties of odorant-binding proteins (OBPs) with β-ionone, we performed gene cloning, evolution analysis, bacterial expression, fluorescence competitive binding assay, and m  ...[more]

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