首页> 美国卫生研究院文献>Journal of Bacteriology >De Novo Biosynthesis of Nicotinamide Adenine Dinucleotide in Escherichia coli: Excretion of Quinolinic Acid by Mutants Lacking Quinolinate Phosphoribosyl Transferase
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De Novo Biosynthesis of Nicotinamide Adenine Dinucleotide in Escherichia coli: Excretion of Quinolinic Acid by Mutants Lacking Quinolinate Phosphoribosyl Transferase

机译:从头生物合成烟酰胺腺嘌呤二核苷酸在大肠杆菌中:缺少喹啉酸酯磷酸核糖基转移酶的突变体对喹啉酸的排泄

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摘要

The excretion of quinolinic acid was studied in growing and resting cells of Escherichia coli K-12 nadC13. Under optimal conditions, this organism could synthesize quinolinic acid in several-fold excess of the amount which would be required for normal growth. The excretion of quinolinic acid was controlled by the concentration of nicotinamide adenine dinucleotide (NAD) precursors available to the organism either during growth or during incubation in dense cell suspensions. These observations suggest that biosynthesis of NAD de novo is regulated by both repression and feedback inhibition. Analogues of niacin which inhibit bacterial growth also inhibited and repressed the synthesis (excretion) of quinolinic acid. The pH optimum for quinolinic acid excretion agreed favorably with the optimum observed for its synthesis in vitro. The rate of quinolinic acid excretion was strongly influenced by the concentration of ribose or glycerol in the medium.
机译:在大肠杆菌K-12 nadC13的生长和静止细胞中研究了喹啉酸的排泄。在最佳条件下,这种生物可以合成喹啉酸,其量是正常生长所需量的几倍。喹啉酸的排泄是通过在致密细胞悬浮液中生长或孵育期间有机体可获得的烟酰胺腺嘌呤二核苷酸(NAD)前体的浓度来控制的。这些观察结果表明,NAD从头的生物合成受阻抑和反馈抑制的调节。烟酸抑制细菌生长的类似物也抑制并抑制了喹啉酸的合成(排泄)。喹啉酸排泄的最适pH值与其体外合成观察到的最适值相吻合。培养基中核糖或甘油的浓度强烈影响喹啉酸的排泄速率。

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