首页> 外文期刊>Journal of Bioscience and Bioengineering >Identification of the Gene Encoding a NAD(P)H-Flavin Oxidoreductase Coupling with Dibenzothiophene (DBT)-Desulfurizing Enzymes from the DBT-Nondesulfurizing Bacterium Paenibacillus polymyxa A-1
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Identification of the Gene Encoding a NAD(P)H-Flavin Oxidoreductase Coupling with Dibenzothiophene (DBT)-Desulfurizing Enzymes from the DBT-Nondesulfurizing Bacterium Paenibacillus polymyxa A-1

机译:从DBT非脱硫细菌多粘芽孢杆菌A-1中编码NAD(P)H-黄酮氧化还原酶与二苯并噻吩(DBT)-脱硫酶偶联的基因的鉴定

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摘要

The gene encoding NAD(P)-H-flavin oxidoreductase (flavin reductase), which couples efficiently with dibenzothiophene (DBT)-desulfurizing monooxygenases of Rhodococci, was cloned from a DBT-non-desulfurizing bacterium Paenibacillus polymyxa A-1 in Escherichia coli, and designated as flv. Cell-free extracts from the recombinant exhibited a flavin reductase activity about forty times higher than that of the E. coli carrying the vector DNA only. Nucleotide sequence analysis reveals that the gene product consists of 208 amino acids and showed about 27%, 32% and 21% identity in amino acid sequence with FRase I, the major flavin reductase of Vibrio fischeri, the NADH dehydrogenase of Thermus thermophilus and several members of the nitroreductase family, respectively. The coexpression of flv with tow kinds of desulfurizing genes, dszABC and tdsABC, in E. coli enhanced the rate of DBT degradation by about 10 and 5 times as high as in the case without flv, respectively.
机译:从非脱硫DBT细菌多粘杆菌A-1中分离出编码NAD(P)-H-黄素氧化还原酶(黄素还原酶)的基因,该基因与红球菌的二苯并噻吩(DBT)脱硫单加氧酶有效偶联。并指定为flv。来自重组体的无细胞提取物显示出黄素还原酶活性,比仅携带载体DNA的大肠杆菌的黄素还原酶活性高约40倍。核苷酸序列分析表明,该基因产物由208个氨基酸组成,与FRase I,费氏弧菌的主要黄素还原酶,嗜热栖热菌的NADH脱氢酶和几个成员在氨基酸序列上具有约27%,32%和21%的同一性。分别为硝基还原酶家族的成员。 flv与两种脱硫基因dszABC和tdsABC在大肠杆菌中的共表达使DBT降解速率分别比没有flv的情况高约10倍和5倍。

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