• 제목/요약/키워드: Carboxylesterase

검색결과 42건 처리시간 0.015초

서양종(西洋種)꿀벌의 살충제분해효소에 관(關)한 연구(硏究) (Enzyme Activities of a Honeybee(Apis mellifera L.) Associated with the Degradation of Some Insecticides)

  • 서용택;심재한
    • Applied Biological Chemistry
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    • 제31권3호
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    • pp.241-248
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    • 1988
  • 서양종(西洋種) 꿀벌(Apis mellifera L)에 대(對)한 살충제의 독성(毒性) 및 해독능력(解毒能力)을 조사(調査)하고 농약한계사용량(農藥限界使用量) 결정(決定)에 기여(寄與)하기 위하여 7가지 대표적(代表的)인 살충제의 꿀벌에 대한 독성(毒性)및 해독효소(解毒酵素)의 활성(活性)을 조사(調査)하였다. 효소활성(酵素活性)은 해독효소(解毒酵素)로 알려진 microsomal oxidases, glutathione S-transferases, esterases 와 DDT-dehydrochlorinase를 조사(調査)했고 성충(成?)일별의 중장(中腸)을 사용(使用)하여 측정(測定)하였다. $LC_{50}$치(値)의 측정결과(測定決果) 공시(供試) 살충제중(殺?劑中) DDT가 58ppm으로 독성(毒性)이 가장 낮았고 EPN이 1.61ppm으로 독성(毒性)이 가장 강(强)했다. 준치사농도(準致死濃度)의 농약(農藥)이 성충(成?)일벌의 microsomal oxidase에 미치는 영향은 malathion 및 permethrin 처리(處理)가 aldrin epoxidase 활성(活性)을 저해(沮害)시켰고 N-demethylase 활성(活性)은 diazinon 처리구(處理區)에서 증대(增大)되었다. Ghtathione S-transferarse(DCNB conjugation) 활성(活性)은 diazinon과 permethrin 처리구(處理區)에서 증대(增大)되었다. Esterase는 malathion 및 permethrin 처리구(處理區)에서 ${\alpha}-NA$ esterase활성(活性)의 저해(沮害)를 보였고 diazinon처리구(處理區)에서 carboxylesterase활성(活性)이 증대(增大)되었으며 AChE 활성(活性)은 거의 영향(影響)이 없었다. DDT-dehy drochlorinase활성(活性)은 carbaryl 및 permethrin 처리구(處理區)에서 증대(增大)되었다.

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Amino acid, fatty acid, and carbohydrate metabolomic profiles with ginsenoside-induced insecticidal efficacy against Ostrinia furnacalis (Guenee)

  • Liu, Shuangli;Wang, Xiaohui;Zhang, Rui;Song, Mingjie;Zhang, Nanqi;Li, Wanying;Wang, Yingping;Xu, Yonghua;Zhang, Lianxue
    • Journal of Ginseng Research
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    • 제44권4호
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    • pp.544-551
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    • 2020
  • Background: Previous studies have shown the insecticidal efficacy of ginsenosides. In the present study, we aimed to investigate the metabolic mechanism related to the inhibitory effect of panaxadiol saponins (PDSs) against the Asian corn borer Ostrinia furnacalis (Guenee). Methods: Third instar larvae of O. furnacalis were fed normal diets with different concentrations of PDSs for 4 days. The consumption index, relative growth rate, approximate digestibility, and conversion of ingested and digested food were recorded. A targeted gas chromatographye-mass spectrometry assay was performed to detect the profiles of amino acids, fatty acids, and carbohydrates in larvae of O. furnacalis. In addition, the activity of detoxification-related enzymes was determined. Results and Conclusions: PDSs decreased the consumption index, relative growth rate, approximate digestibility, and conversion of ingested and digested food in the 3rd instar larvae of O. furnacalis in a dose-dependent manner. PDSs decreased 15 free amino acids, 16 free fatty acids, and 5 carbohydrates and increased the levels of palmitoleic acid, palmitic acid, and 9-octadecenoic acid in the 3rd instar larvae. The activity of detoxification-related enzymes, such as acetylcholinesterase, glutathione S-transferase, cytochrome P450, carboxylesterase, trehalase, acid phosphatase, and alkaline phosphatase, was reduced in a dose-dependent manner in the 3rd instar larvae exposed to PDSs. These data confirmed the inhibitory effect of PDSs against growth, food utilization, and detoxification in the 3rd instar larvae of O. furnacalis and the potential for using PDSs as an efficient tool for insect pest management for O. furnacalis larvae.