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Oxidative phosphorylation in Escherichia coli K 12. Mutations affecting magnesium ion- or calcium ion-stimulated adenosine triphosphatase

机译:大肠杆菌K 12中的氧化磷酸化。影响镁离子或钙离子刺激的腺苷三磷酸酶的突变。

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p1. Two mutants of iEscherichia coli/i K 12 were isolated which, although able to grow on glucose, are unable to grow with succinate or d-lactate as the sole source of carbon. 2. Genetic mapping of these mutants showed that they both contain a mutation in a gene (designated iuncA/i) mapping at about minute 73.5 on the iE. coli/i chromosome. 3. The iuncA/isup-/sup alleles were transferred by bacteriophage-mediated transduction into another strain of iE. coli/i and the transductants compared with the parent strain to determine the nature of the biochemical lesion in the mutants. 4. The mutants gave low aerobic growth yields when grown on limiting concentrations of glucose, but oxidase activities in membranes from both the mutants and the normal strain were similar. 5. Measurement of P/O ratios with d-lactate as substrate indicated that a mutation in the iuncA/i gene causes uncoupling of phosphorylation associated with electron transport. 6. Determination of the Mgsup2+/sup,Casup2+/sup-stimulated adenosine triphosphatase activities in the mutant and normal strains indicated that the iuncA/i gene is probably the structural gene for Mgsup2+/sup,Casup2+/sup-stimulated adenosine triphosphatase. 7. Mgsup2+/sup,Casup2+/sup-stimulated adenosine triphosphatase therefore appears to be essential for oxidative phosphorylation in iE. coli/i./p
机译:> 1。分离出两个大肠杆菌K 12突变体,尽管它们能够在葡萄糖上生长,但不能以琥珀酸或d-乳酸作为唯一碳源生长。 2.这些突变体的遗传图谱显示,它们都包含一个基因(命名为 uncA )中的突变,该基因位于 E上大约73.5分钟。大肠染色体。 3. uncA -等位基因通过噬菌体介导的转导转移至另一株 E。大肠杆菌和转导子与亲本菌株进行比较,以确定突变体中生化病变的性质。 4.当在有限的葡萄糖浓度下生长时,突变体的需氧生长量较低,但是突变体和正常菌株的膜中的氧化酶活性相似。 5.以d-乳酸盐为底物的P / O比的测量表明, uncA 基因的突变引起与电子运输有关的磷酸化的解偶联。 6.在突变体和正常菌株中Mg 2 + ,Ca 2 + 刺激的腺苷三磷酸酶活性的测定表明 uncA 基因是可能是Mg 2 + ,Ca 2 + 刺激的腺苷三磷酸酶的结构基因。 7.因此,Mg 2 + ,Ca 2 + 刺激的腺苷三磷酸酶似乎对 E的氧化磷酸化至关重要。大肠杆菌

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