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Characterization of MaltOBP1, a Minus-C Odorant-Binding Protein, From the Japanese Pine Sawyer Beetle, Monochamus alternatus Hope (Coleoptera: Cerambycidae)

Insect Odorant-Binding Proteins (OBPs) play crucial roles in the discrimination, binding and transportation of odorants. Herein, the full-length cDNA sequence of Minus-C OBP1 (MaltOBP1) from the Japanese pine sawyer beetle, Monochamus alternatus, was cloned by 3′ and 5′ RACE-PCR and analyzed. The re...

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Autores principales: Zhang, Fangmei, Merchant, Austin, Zhao, Zhibin, Zhang, Yunhui, Zhang, Jing, Zhang, Qingwen, Wang, Qinghua, Zhou, Xuguo, Li, Xiangrui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7138900/
https://www.ncbi.nlm.nih.gov/pubmed/32296339
http://dx.doi.org/10.3389/fphys.2020.00212
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author Zhang, Fangmei
Merchant, Austin
Zhao, Zhibin
Zhang, Yunhui
Zhang, Jing
Zhang, Qingwen
Wang, Qinghua
Zhou, Xuguo
Li, Xiangrui
author_facet Zhang, Fangmei
Merchant, Austin
Zhao, Zhibin
Zhang, Yunhui
Zhang, Jing
Zhang, Qingwen
Wang, Qinghua
Zhou, Xuguo
Li, Xiangrui
author_sort Zhang, Fangmei
collection PubMed
description Insect Odorant-Binding Proteins (OBPs) play crucial roles in the discrimination, binding and transportation of odorants. Herein, the full-length cDNA sequence of Minus-C OBP1 (MaltOBP1) from the Japanese pine sawyer beetle, Monochamus alternatus, was cloned by 3′ and 5′ RACE-PCR and analyzed. The results showed that MaltOBP1 contains a 435 bp open reading frame (ORF) that encodes 144 amino acids, including a 21-amino acid signal peptide at the N-terminus. The matured MaltOBP1 protein possesses a predicted molecular weight of about 14 kDa and consists of six α-helices, creating an open binding pocket, and two disulfide bridges. Immunoblotting results showed that MaltOBP1 was most highly expressed in antennae in both sexes, followed by wings and legs. Fluorescence assays demonstrated that MaltOBP1 protein exhibited high binding affinity with (R)-(+)-α-pinene, (−)-β-pinene, trans-caryophyllene, (R)-(+)-limonene and (–)-verbenone, which are the main volatile compounds of the pine tree. Our combined results suggest that MaltOBP1 plays a role in host seeking behavior in M. alternatus.
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spelling pubmed-71389002020-04-15 Characterization of MaltOBP1, a Minus-C Odorant-Binding Protein, From the Japanese Pine Sawyer Beetle, Monochamus alternatus Hope (Coleoptera: Cerambycidae) Zhang, Fangmei Merchant, Austin Zhao, Zhibin Zhang, Yunhui Zhang, Jing Zhang, Qingwen Wang, Qinghua Zhou, Xuguo Li, Xiangrui Front Physiol Physiology Insect Odorant-Binding Proteins (OBPs) play crucial roles in the discrimination, binding and transportation of odorants. Herein, the full-length cDNA sequence of Minus-C OBP1 (MaltOBP1) from the Japanese pine sawyer beetle, Monochamus alternatus, was cloned by 3′ and 5′ RACE-PCR and analyzed. The results showed that MaltOBP1 contains a 435 bp open reading frame (ORF) that encodes 144 amino acids, including a 21-amino acid signal peptide at the N-terminus. The matured MaltOBP1 protein possesses a predicted molecular weight of about 14 kDa and consists of six α-helices, creating an open binding pocket, and two disulfide bridges. Immunoblotting results showed that MaltOBP1 was most highly expressed in antennae in both sexes, followed by wings and legs. Fluorescence assays demonstrated that MaltOBP1 protein exhibited high binding affinity with (R)-(+)-α-pinene, (−)-β-pinene, trans-caryophyllene, (R)-(+)-limonene and (–)-verbenone, which are the main volatile compounds of the pine tree. Our combined results suggest that MaltOBP1 plays a role in host seeking behavior in M. alternatus. Frontiers Media S.A. 2020-04-01 /pmc/articles/PMC7138900/ /pubmed/32296339 http://dx.doi.org/10.3389/fphys.2020.00212 Text en Copyright © 2020 Zhang, Merchant, Zhao, Zhang, Zhang, Zhang, Wang, Zhou and Li. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Zhang, Fangmei
Merchant, Austin
Zhao, Zhibin
Zhang, Yunhui
Zhang, Jing
Zhang, Qingwen
Wang, Qinghua
Zhou, Xuguo
Li, Xiangrui
Characterization of MaltOBP1, a Minus-C Odorant-Binding Protein, From the Japanese Pine Sawyer Beetle, Monochamus alternatus Hope (Coleoptera: Cerambycidae)
title Characterization of MaltOBP1, a Minus-C Odorant-Binding Protein, From the Japanese Pine Sawyer Beetle, Monochamus alternatus Hope (Coleoptera: Cerambycidae)
title_full Characterization of MaltOBP1, a Minus-C Odorant-Binding Protein, From the Japanese Pine Sawyer Beetle, Monochamus alternatus Hope (Coleoptera: Cerambycidae)
title_fullStr Characterization of MaltOBP1, a Minus-C Odorant-Binding Protein, From the Japanese Pine Sawyer Beetle, Monochamus alternatus Hope (Coleoptera: Cerambycidae)
title_full_unstemmed Characterization of MaltOBP1, a Minus-C Odorant-Binding Protein, From the Japanese Pine Sawyer Beetle, Monochamus alternatus Hope (Coleoptera: Cerambycidae)
title_short Characterization of MaltOBP1, a Minus-C Odorant-Binding Protein, From the Japanese Pine Sawyer Beetle, Monochamus alternatus Hope (Coleoptera: Cerambycidae)
title_sort characterization of maltobp1, a minus-c odorant-binding protein, from the japanese pine sawyer beetle, monochamus alternatus hope (coleoptera: cerambycidae)
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7138900/
https://www.ncbi.nlm.nih.gov/pubmed/32296339
http://dx.doi.org/10.3389/fphys.2020.00212
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