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Truncation Mutants Highlight a Critical Role for the N- and C-termini of the Spirulina Δ6 Desaturase in Determining Regioselectivity

机译:截短突变体突出了螺旋藻Δ6去饱和酶的N和C末端在确定区域选择性中的关键作用

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The results of our previous study on heterologous expression in Escherichia coli of the gene desD, which encodes Spirulina Δ6 desaturase, showed that co-expression with an immediate electron donor—either cytochrome b 5 or ferredoxin—was required for the production of GLA (γ-linolenic acid), the product of the reaction catalyzed by Δ6 desaturase. Since a system for stable transformation of Spirulina is not available, studies concerning Spirulina-enzyme characterization have been carried out in heterologous hosts. In this present study, the focus is on the role of the enzyme’s N- and C-termini, which are possibly located in the cytoplasmic phase. Truncated enzymes were expressed in E. coli by employing the pTrcHisA expression system. The truncation of the N- and C-terminus by 10 (N10 and C10) and 30 (N30 and C30) amino acids, respectively, altered the enzyme’s regioselective mode from one that measures from a preexisting double bond to that measuring from the methyl end of the substrate.
机译:我们先前对编码螺旋藻Δ6去饱和酶的desD基因在大肠杆菌中异源表达的研究结果表明,与直接电子供体(细胞色素b 5 或铁氧还蛋白)共表达是由Δ6去饱和酶催化的反应产物GLA(γ-亚麻酸)所必需的。由于没有用于螺旋藻稳定转化的系统,因此已经在异源宿主中进行了关于螺旋藻酶表征的研究。在本研究中,重点是酶的N末端和C末端的作用,它们可能位于细胞质期。通过使用pTrcHisA表达系统,截短的酶在大肠杆菌中表达。 N端和C端分别被10个(N10和C10)和30个(N30和C30)氨基酸截短,改变了该酶的区域选择性模式,从先前存在的双键改变为甲基末端基板的

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