首页> 外文期刊>FEMS Microbiology Letters >Identification of Pantoea ananatis gene encoding membrane pyrroloquinoline quinone (PQQ)-dependent glucose dehydrogenase and pqqABCDEFoperon essential for PQQ biosynthesis
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Identification of Pantoea ananatis gene encoding membrane pyrroloquinoline quinone (PQQ)-dependent glucose dehydrogenase and pqqABCDEFoperon essential for PQQ biosynthesis

机译:泛膜编码吡咯并喹啉醌(PQQ)的葡萄糖脱氢酶和PqqABCDEFoperon对PQQ生物合成必不可少的泛酸基因的鉴定。

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Pantoea ananatis accumulates gluconate during aerobic growth in the presence of glucose. Computer analysis of the P. ananatis SC17(0) sequenced genome revealed an ORF encoding a homologue (named gcd) of the mGDH (EC 1.1.99.17) apoenzyme from Escherichia coli and a putative pyrroloquinoline quinone (PQQ) biosynthetic operon homologous to pqqABCDEF from Klebsiella pneumoniae. Construction of Δgcd and Δpqq mutants of P. ananatis confirmed the proposed functions of these genetic elements. The P. ananatis pqqABCDEF was cloned in vivo and integrated into the chromosomes of P. ananatis and E. coli according to the Dual In/Out strategy. Introduction of a second copy of pqqABCDEF to P. ananatis SC17(0) doubled the accumulation of PQQ. Integration of the operon into E. coli MG1655ΔptsGΔmanXY restored the growth of bacteria on glucose. The obtained data show the essential role of pqqABCDEF in PQQ biosynthesis in P. ananatis and E. coli. We propose that the cloned operon could be useful for an efficient phosphoenolpyruvate-independent glucose consumption pathway due to glucose oxidation and construction of E. coli strains with the advantage of phosphoenolpyruvate-derived metabolite production.
机译:在有葡萄糖的情况下,无氧细菌在有氧生长过程中会积累葡萄糖酸盐。对香蕉假单胞菌SC17(0)测序基因组的计算机分析显示,ORF编码来自大肠杆菌的mGDH(EC 1.1.99.17)脱辅酶的同源物(命名为gcd)和与来自pqqABCDEF同源的推定的吡咯并喹啉醌(PQQ)生物合成操纵子肺炎克雷伯菌。菠萝假单胞菌的Δgcd和Δpqq突变体的构建证实了这些遗传元件的拟议功能。根据双重输入/输出策略,将P. ananatis pqqABCDEF体内克隆并整合到P. ananatis和大肠杆菌的染色体中。将pqqABCDEF的第二个副本引入到菠萝假单胞菌SC17(0)中,使PQQ的积累增加了一倍。操纵子整合到大肠杆菌MG1655ΔptsGΔmanXY中可恢复细菌在葡萄糖上的生长。所获得的数据表明pqqABCDEF在凤梨假单胞菌和大肠杆菌的PQQ生物合成中起着至关重要的作用。我们提出,由于葡萄糖氧化和大肠杆菌菌株的构建,利用磷酸烯醇丙酮酸衍生的代谢产物的优势,克隆的操纵子可用于有效的磷酸烯醇丙酮酸非依赖性葡萄糖消耗途径。

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