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

被引:20
|
作者
Zhang, Fangmei [1 ,2 ]
Merchant, Austin [3 ]
Zhao, Zhibin [4 ]
Zhang, Yunhui [2 ]
Zhang, Jing [5 ]
Zhang, Qingwen [5 ]
Wang, Qinghua [6 ]
Zhou, Xuguo [3 ]
Li, Xiangrui [2 ,3 ]
机构
[1] Xinyang Agr & Forestry Univ, Henan Prov South Henan Crop Pest Green Prevent &, Xinyang, Peoples R China
[2] Chinese Acad Agr Sci, State Key Lab Biol Plant Dis & Insect Pests, Inst Plant Protect, Beijing, Peoples R China
[3] Univ Kentucky, Dept Entomol, Lexington, KY USA
[4] Chongqing Univ, Coll Bioengn, Minist Educ, Key Lab Biorheol Sci & Technol, Chongqing, Peoples R China
[5] China Agr Univ, Dept Entomol, Beijing, Peoples R China
[6] Chinese Acad Forestry, Key Lab Forest Protect, State Forestry Adm China, Res Inst Forest Ecol Environm & Protect, Beijing, Peoples R China
来源
FRONTIERS IN PHYSIOLOGY | 2020年 / 11卷
关键词
Monochamus alternatus; olfactory; odorant binding protein; fluorescence binding assay; plant volatile; CHEMOSENSORY GENE FAMILIES; LIGAND-BINDING; PHEROMONE-BINDING; SEQUENCE-ANALYSIS; CRYSTAL-STRUCTURE; HOST VOLATILES; EXPRESSION; VECTOR; IDENTIFICATION; ATTRACTION;
D O I
10.3389/fphys.2020.00212
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
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 alpha-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)-(+)-alpha-pinene, (-)-beta-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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页数:10
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