粘虫
几丁质酶
玉米螟
生殖器鳞翅目
夜蛾
生物
杀虫剂
恶二唑虫
有害生物分析
毒理
植物
生物化学
酶
基因
生态学
重组DNA
作者
Qiong Lu,Li‐Ping Xu,Lin Liu,Yong Zhou,Tian Liu,Yongxiang Song,Jianhua Ju,Qing Yang
标识
DOI:10.1021/acs.jafc.1c05385
摘要
Insect group h chitinase is a promising target for designing non-target safe pesticides in that it is exclusively distributed in lepidopteran insects, over 80% of which are agricultural pests. In this work, lynamicin B was discovered to be an inhibitor of OfChi-h, the group h chitinase from the lepidopteran pest Ostrinia furnacalis. Lynamicin B was revealed to competitively inhibit OfChi-h with a Ki value of 8.76 μM and does not significantly inhibit other chitinases. The co-crystal structure of lynamicin B and OfChi-h revealed that the dichloroindolyl group of lynamicin B occupies an unexplored pocket below subsites +1 and +2 of the substrate-binding cleft, which is vital for its selectivity. Feeding experiments demonstrated that lynamicin B exhibited high insecticidal activities against other lepidopteran pests Mythimna separata and Spodoptera frugiperda besides O. furnacalis. Moreover, lynamicin B did not affect Trichogramma ostriniae, a natural enemy of O. furnacalis. This study provides a natural-derived potent pesticide for the control of lepidopteran pests, leaving its natural enemy unaffected.
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