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Identification of Novel Polyphenolic Inhibitors of Shikimate Dehydrogenase (AroE)

机译:新型Shikimate脱氢酶(AroE)多酚抑制剂的鉴定

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Shikimate dehydrogenase (AroE) is an attractive target for herbicides and antimicrobial agents due to its conserved and essential nature in plants, fungi, and bacteria. Here, we have performed an in vitro screen using a collection of more than 5500 compounds and identified 24 novel inhibitors of AroE from Pseudomonas putida. The IC_(50) values for the two most potent inhibitors we identified, epigallocatechin gallate (EGCG) and epicatechin gallate (ECG), were 3.0 ± 0.2 μM and 3.7 ± 0.5 μM, respectively. Based on the high level of structural conservation between AroE orthologs, we predicted that the identified compounds would also inhibit AroE enzymes from other organisms. Consistent with this hypothesis, we found that EGCG and ECG inhibit the AroE domain of the bifunctional dehydroquinate dehydratase-shikimate dehydrogenase (DHQ-SDH) from Arabidopsis thaliana with IC_(50) values of 2.1 ± 0.3 μM and 2.0 ± 0.2 μM, respectively.
机译:Shikimate脱氢酶(AroE)由于在植物,真菌和细菌中的保守和必要性质而成为除草剂和抗菌剂的诱人靶标。在这里,我们使用了5500多种化合物进行了体外筛选,并从恶臭假单胞菌中鉴定了24种新型AroE抑制剂。我们确定的两种最有效的抑制剂表没食子儿茶素没食子酸酯(EGCG)和表儿茶素没食子酸酯(ECG)的IC_(50)值分别为3.0±0.2μM和3.7±0.5μM。基于AroE直系同源物之间的高水平结构保守性,我们预测所鉴定的化合物也将抑制其他生物的AroE酶。与此假设相符,我们发现EGCG和ECG抑制了拟南芥双功能脱氢奎宁脱水酶-shi草酸脱氢酶(DHQ-SDH)的AroE域,IC_(50)值分别为2.1±0.3μM和2.0±0.2μM。

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