首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Cloning and expression of the gene cluster encoding key proteins involved in acetyl-CoA synthesis in Clostridium thermoaceticum: CO dehydrogenase the corrinoid/Fe-S protein and methyltransferase.
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Cloning and expression of the gene cluster encoding key proteins involved in acetyl-CoA synthesis in Clostridium thermoaceticum: CO dehydrogenase the corrinoid/Fe-S protein and methyltransferase.

机译:在热乙酸梭菌中编码与乙酰辅酶A合成有关的关键蛋白的基因簇的克隆和表达:CO脱氢酶类rinrin / Fe-S蛋白和甲基转移酶。

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摘要

Acetogenic bacteria fix CO or CO2 by a pathway of autotrophic growth called the acetyl-CoA (or Wood) pathway. Key enzymes in the pathway are a methyltransferase, a corrinoid/Fe-S protein, a disulfide reductase, and a carbon monoxide dehydrogenase. This manuscript describes the isolation of the genes that code for the methyltransferase, the two subunits of the corrinoid/Fe-S protein, and the two subunits of carbon monoxide dehydrogenase. These five genes were found to be clustered within an approximately 10-kilobase segment on the Clostridium thermoaceticum genome. The proteins were expressed at up to 5-10% of Escherichia coli cell protein, and isopropyl beta-D-thiogalactopyranoside had no effect on the levels of expression, implying that the C. thermoaceticum inserts contained transcriptional and translational signals that were recognized by E. coli. The methyltransferase is expressed in E. coli in a fully active dimeric form with a specific activity and heat stability similar to the enzyme expressed in C. thermoaceticum. However, both the corrinoid/Fe-S protein and carbon dioxide dehydrogenase, although expressed in high amounts and with identical subunit molecular weights in E. coli, are inactive and less heat stable than are the native enzymes from C. thermoaceticum.
机译:产乙酸细菌通过自养生长途径(称为乙酰辅酶A(或木材)途径)固定CO或CO2。该途径中的关键酶是甲基转移酶,类corrinoid / Fe-S蛋白,二硫键还原酶和一氧化碳脱氢酶。该手稿描述了编码甲基转移酶,类corrinoid / Fe-S蛋白的两个亚基以及一氧化碳脱氢酶的两个亚基的基因的分离。发现这五个基因聚集在热乙酸梭状芽胞杆菌基因组的大约10个碱基的片段内。这些蛋白质最多可表达大肠杆菌细胞蛋白质的5-10%,而异丙基β-D-硫代半乳糖吡喃糖苷对表达水平没有影响,这表明嗜热梭状芽胞杆菌插入物含​​有被E识别的转录和翻译信号。大肠杆菌甲基转移酶以完全活性的二聚体形式在大肠杆菌中表达,其特异性活性和热稳定性类似于在热乙酸梭菌中表达的酶。然而,尽管在大肠杆菌中表达量高且亚单位分子量相同,但类corrinoid / Fe-S蛋白和二氧化碳脱氢酶均比来自热乙酸梭菌的天然酶无活性且热稳定性较差。

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