首页> 美国卫生研究院文献>Journal of Bacteriology >Screening of Environmental DNA Libraries for the Presence of Genes Conferring Na+(Li+)/H+ Antiporter Activity on Escherichia coli: Characterization of the Recovered Genes and the Corresponding Gene Products
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Screening of Environmental DNA Libraries for the Presence of Genes Conferring Na+(Li+)/H+ Antiporter Activity on Escherichia coli: Characterization of the Recovered Genes and the Corresponding Gene Products

机译:筛选环境DNA库中是否存在赋予大肠杆菌Na +(Li +)/ H +反转运蛋白活性的基因:回收基因和相应基因产物的表征

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摘要

Environmental DNA libraries prepared from three different soils were screened for genes conferring Na+(Li+)/H+ antiporter activity on the antiporter-deficient Escherichia coli strain KNabc. The presence of those genes was verified on selective LK agar containing 7.5 mM LiCl. Two positive E. coli clones were obtained during the initial screening of 1,480,000 recombinant E. coli strains. Both clones harbored a plasmid (pAM1 and pAM3) that conferred a stable Li+-resistant phenotype. The insert of pAM2 (1,886 bp) derived from pAM1 contained a gene (1,185 bp) which encodes a novel Na+/H+ antiporter belonging to the NhaA family. The insert of pAM3 harbored the DNA region of E. coli K-12 containing nhaA, nhaR, and gef. This region is flanked by highly conserved insertion elements. The sequence identity with E. coli decreased significantly outside of the insertion sequence elements, indicating that the unknown organism from which the insert of pAM3 was cloned is different from E. coli. The products of the antiporter genes located on pAM2 and pAM3 revealed functional homology to NhaA of E. coli and enabled the antiporter-deficient E. coli mutant to grow on solid media in the presence of up to 450 mM NaCl or 250 mM LiCl at pH 8.0. The Na+/H+ antiporter activity in everted membrane vesicles that were derived from the E. coli strains KNabc/pAM2 and KNabc/pAM3 showed a substantial increase between pHs 7 and 8.5. The maximal activity was observed at pHs 8.3 and 8.6, respectively. The Kmvalues of both antiporters for Na+ were approximately 10-fold higher than the values for Li+.
机译:筛选从三种不同土壤制备的环境DNA文库中是否存在赋予Na + (Li + )/ H + 反向转运蛋白活性的基因大肠杆菌菌株KNabc。在含有7.5 mM LiCl的选择性LK琼脂上验证了这些基因的存在。在初步筛选1,480,000重组大肠杆菌菌株期间获得了两个阳性大肠杆菌克隆。两个克隆都带有一个质粒(pAM1和pAM3),该质粒具有稳定的Li + 耐药表型。源自pAM1的pAM2的插入片段(1,886 bp)包含一个基因(1,185 bp),该基因编码属于NhaA家族的新型Na + / H + 反转运蛋白。 pAM3的插入片段包含E.coli K-12的DNA区域,其中包含nhaA,nhaR和gef。该区域的侧面是高度保守的插入元件。在插入序列元件之外,与大肠杆菌的序列同一性显着降低,这表明克隆了pAM3插入物的未知生物不同于大肠杆菌。位于pAM2和pAM3上的反转运蛋白基因产物显示出与大肠杆菌NhaA的功能同源性,并使反转运蛋白缺陷型大肠杆菌突变体能够在pH高达450 mM NaCl或250 mM LiCl的固体培养基上生长8.0。从大肠杆菌菌株KNabc / pAM2和KNabc / pAM3衍生的外翻膜囊泡中的Na + / H + 反向转运蛋白活性在pH值7和7之间显着增加。 8.5。在pH 8.3和8.6分别观察到最大活性。 Na + 的两个反转运蛋白的Km值大约比Li + 的Km值高10倍。

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