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首页> 外文期刊>Plant physiology >Study of the 3-hydroxy eicosanoyl-coenzyme A dehydratase and (E)-2,3 enoyl-coenzyme a reductase involved in acyl-coenzyme a elongation in etiolated leek seedlings
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Study of the 3-hydroxy eicosanoyl-coenzyme A dehydratase and (E)-2,3 enoyl-coenzyme a reductase involved in acyl-coenzyme a elongation in etiolated leek seedlings

机译:韭菜幼苗中3-羟基二十碳酰基辅酶A脱水酶和(E)-2,3-烯酰基辅酶a还原酶参与酰基辅酶伸长的研究

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(R,S)-[1- superior 1 superior 4C]3-Hydroxy eicosanoyl-coenzyme A (CoA) has been chemically synthesized to study the 3-hydroxy acyl-CoA dehydratase involved in the acyl-CoA elongase of etiolated leek (Allium porrum L.) seedling microsomes. 3-Hydroxy eicosanoyl-CoA (3-OH C20:0-CoA) dehydration led to the formation of (E)-2,3 eicosanoyl-CoA, which has been characterized. Our kinetic studies have determined the optimal conditions of the dehydration and also resolved the stereospecificity requirement of the dehydratase for (R)-3-OH C20:0-CoA. Isotopic dilution experiments showed that 3-hydroxy acyl-CoA dehydratase had a marked preference for (R)3-OH C20:0-CoA. Moreover, the very-long-chain synthesis using (R)-3-OH C20:0-CoA isomer and [2- superior 1 superior 4C]malonyl-CoA was higher than that using the (S) isomer, whatever the malonyl-CoA and the 3-OH C20:0-CoA concentrations. We have also used [1- superior 1 superior 4C]3-OH C20:0-CoA to investigate the reductant requirement of the enoyl-CoA reductase of the acyl-CoA elongase complex. In the presence of NADPH, [1- superior 1 superior 4C]3-OH C20:0-CoA conversion was stimulated. Aside from the product of dehydration, i.e. (E)-2,3 eicosanoyl-CoA, we detected eicosanoyl-CoA resulting from the reduction of (E)-2,3 eicosanoyl-CoA. When we replaced NADPH with NADH, the eicosanoyl-CoA was 8- to 10-fold less abundant. Finally, in the presence of malonyl-CoA and NADPH or NADH, [1- superior 1 superior 4C]3-OH C20: 0-CoA led to the synthesis of very-long-chain fatty acids. This synthesis was measured using [1- superior 1 superior 4C]3-OH C20:0-CoA and malonyl-CoA or (E)-2,3 eicosanoyl-CoA and [2- superior 1 superior 4C]malonyl-CoA. In both conditions and in the presence of NADPH, the acyl-CoA elongation activity was about 60 nmol mg superior - superior 1 h superior - superior 1, which is the highest ever reported for a plant system.
机译:(R,S)-[1-高级1高级4C] 3-羟基二十碳酰辅酶A(CoA)已被化学合成以研究参与黄化韭菜的酰基-CoA延长酶的3-羟基酰基-CoA脱水酶porum L.)幼苗微粒体。 3-羟基二十烷酰基-CoA(3-OH C20:0-CoA)脱水导致形成(E)-2,3-二十烷酰基-CoA,已被表征。我们的动力学研究确定了脱水的最佳条件,并解决了脱水酶对(R)-3-OH C20:0-CoA的立体定向性要求。同位素稀释实验表明,3-羟基酰基-CoA脱水酶对(R)3-OH C20:0-CoA具有明显的偏爱。此外,无论丙二酰基-丙二酰基-丙二酰基-丙二酰基-(C):0-CoA异构体和[2-高级1高级4C]丙二酰基-CoA的超长链合成均高于使用(S)异构体的长链。 CoA和3-OH C20:0-CoA浓度。我们还使用了[1-优1优4C] 3-OH C20:0-CoA来研究酰基-CoA延长酶复合物的烯酰-CoA还原酶的还原剂要求。在NADPH存在下,刺激了[1-高级1高级4C] 3-OH C20:0-CoA转化。除了脱水产物即(E)-2,3二十碳酰基-CoA,我们还检测到由于(E)-2,3二十碳酰基-CoA的还原而产生的二十碳酰基-CoA。当我们用NADH代替NADPH时,二十碳酰辅酶A的丰度降低了8到10倍。最后,在丙二酰辅酶A和NADPH或NADH的存在下,[1-高级1高级4C] 3-OH C20:0-CoA导致了非常长链脂肪酸的合成。使用[1-高级1高级4C] 3-OH C20:0-CoA和丙二酰基-CoA或(E)-2,3二十碳酰基-CoA和[2-高级1高级4C]丙二酰基-CoA测量该合成。在两种条件下以及在存在NADPH的情况下,酰基辅酶A的延伸活性均优越约60 nmol mg-优越1 h-优越1,这是植物系统报道的最高值。

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