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Functional analysis of orthologous artemisinic aldehyde Δ11(13)-reductase reveals potential artemisinin-producing activity in non-artemisinin-producing Artemisia absinthium

机译:直系同源青蒿醛Δ11(13)-还原酶的功能分析揭示了在非青蒿素生产的苦艾中的潜在青蒿素生产活性

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Artemisinin is the most effective antimalarial compound isolated from Artemisia annua . Artemisinic aldehyde Δ11(13)-reductase (DBR2) catalyzes the reduction of artemisinic aldehyde into dihydroartemisinic aldehyde, switching the pathway towards artemisinin production. Although other Artemisia species cannot produce artemisinin, we found a putative DBR2 ortholog expressed in A. absinthium ( abDBR2 ). We examined the catalytic activity of abDBR2 in vitro and found that it shows comparable activity to that of DBR2 based on the reduction of artemisinic aldehyde into dihydroartemisinic aldehyde. Furthermore, we found that dihydroartemisinic aldehyde was detected in the extract of A. absinthium leaves fed with artemisinic aldehyde, suggesting the presence of active abDBR2 in planta . Our results indicate that A. absinthium may be a potential host for the production of artemisinin through metabolic engineering.
机译:青蒿素是从青蒿中分离出的最有效的抗疟化合物。青蒿醛Δ11(13)-还原酶(DBR2)催化将青蒿醛还原为二氢青蒿醛,从而切换了青蒿素生产的途径。尽管其他蒿属物种无法产生青蒿素,但我们发现了在假山曲霉(abDBR2)中表达的推定DBR2直系同源物。我们在体外检查了abDBR2的催化活性,发现基于青蒿醛还原为二氢青蒿醛,它显示出与DBR2相当的活性。此外,我们发现在饲喂青蒿醛的苦艾叶提取物中检测到二氢青蒿醛,表明植物中存在活性abDBR2。我们的结果表明苦艾酒可能是通过代谢工程生产青蒿素的潜在宿主。

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