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首页> 外文期刊>Journal of Bioscience and Bioengineering >Cloning, sequencing and expression analysis of a gene encoding alcohol oxidase in Paenibacillus sp. AIU 311
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Cloning, sequencing and expression analysis of a gene encoding alcohol oxidase in Paenibacillus sp. AIU 311

机译:Paenibacillus sp。中编码乙醇氧化酶的基因的克隆,测序和表达分析。 AIU 311

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摘要

We have cloned a gene encoding an alcohol oxidase (AOD) specific to aldehyde alcohols from Paenibacillus sp. AIU 311. The AOD gene contains an open reading frame consisting of 618 nucleotides corresponding to 205 amino acid residues. The deduced amino acid sequence exhibits a high similarity to that of manganese superoxide dismutases (SODs). We expressed the cloned gene as an active product in Escherichia coli BL21 cells. The productivity (total units per culture broth volume) of the recombinant AOD expressed in E. coli BL21 is 26,000-fold higher than that of AOD in Paenibacillus sp. AIU 311. The recombinant AOD also exhibits aldehyde alcohol oxidase activity and SOD activity. The recombinant cells described in this study have utility for the production of glyoxal from glycolaldehyde.
机译:我们已经克隆了一种编码来自Paenibacillus sp。的醛醇的醇氧化酶(AOD)的基因。 AIU 311. AOD基因包含一个开放阅读框,该框架由对应于205个氨基酸残基的618个核苷酸组成。推导的氨基酸序列与锰超氧化物歧化酶(SODs)具有高度相似性。我们将克隆的基因表达为大肠杆菌BL21细胞中的活性产物。在大肠杆菌BL21中表达的重组AOD的生产力(每培养液总体积单位)比Paenibacillus sp。中的AOD的生产力高26,000倍。 AIU 311.重组AOD还表现出醛醇氧化酶活性和SOD活性。这项研究中描述的重组细胞可用于由乙醇醛生产乙二醛。

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