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Mono- and di-thiocarbamate inhibition studies of the δ-carbonic anhydrase TweCAδ from the marine diatom Thalassiosira weissflogii

机译:海洋硅藻Thalassiosira weissflogii的δ-碳酸酐酶TweCAδ的单硫代和二硫代氨基甲酸酯抑制研究

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摘要

The inhibition of the δ-class carbonic anhydrase (CAs, EC 4.2.1.1) from the diatom Thalassiosira weissflogii, TweCAδ, was investigated using a panel of 36 mono- and di-thiocarbamates chemotypes that have recently been shown to inhibit mammalian and pathogenic CAs belonging to the α- and β-classes. TweCAδ was not significantly inhibited by most of such compounds (KI values above 20 µM). However, some aliphatic, heterocyclic, and aromatic mono and di-thiocarbamates inhibited TweCAδ in the low micromolar range. For some compounds incorporating the piperazine ring, TweCAδ was effectively inhibited (KIs from 129 to 791 nM). The most effective inhibitors identified in this study were 3,4-dimethoxyphenyl-ethyl-mono-thiocarbamate (KI of 67.7 nM) and the R-enantiomer of the nipecotic acid di-thiocarbamate (KI of 93.6 nM). Given that the activity and inhibition of this class of enzyme have received limited attention until now, this study provides new molecular probes and information for investigating the role of δ-CAs in the carbon fixation processes in diatoms, which are responsible for significant amounts of CO2 taken from the atmosphere by these marine organisms.
机译:使用一组36种单硫代和二硫代氨基甲酸酯化学型研究了硅藻Thalassiosira weissflogiiTweCAδ对δ级碳酸酐酶(CAs,EC 4.2.1.1)的抑制作用,这些化合物最近被证明可以抑制哺乳动物和致病性CAs。属于α和β类。大多数此类化合物(KI值高于20 µM)并未显着抑制TweCAδ。但是,一些脂族,杂环和芳族单和二硫代氨基甲酸酯在低微摩尔范围内抑制TweCAδ。对于某些掺入哌嗪环的化合物,TweCAδ被有效抑制(KIs从129至791 nM)。在这项研究中鉴定出的最有效的抑制剂是3,4-二甲氧基苯基-乙基-单-硫代氨基甲酸酯(KI为67.7MnM)和乳酸酸二硫代氨基甲酸酯的R-对映体(KI为93.6 nM)。鉴于到目前为止,这类酶的活性和抑制作用一直受到关注,本研究为研究δ-CA在硅藻碳固定过程中的作用提供了新的分子探针和信息,而硅藻负责大量的CO2。这些海洋生物从大气中提取的。

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