首页> 美国卫生研究院文献>Biochemical Journal >The control of ribonucleic acid synthesis in bacteria. Polymerization rates for ribonucleic acids in amino acid-starved relaxed and stringent auxotrophs of Escherichia coli
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The control of ribonucleic acid synthesis in bacteria. Polymerization rates for ribonucleic acids in amino acid-starved relaxed and stringent auxotrophs of Escherichia coli

机译:细菌中核糖核酸合成的控制。大肠杆菌缺乏氨基酸的松弛和严格营养缺陷型中核糖核酸的聚合速率

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摘要

Polymerization rates of newly formed chains of various RNA fractions were measured in Escherichia coli CP78 (RCstr) and CP79 (RCrel) multiple amino acid auxotrophs, deprived of four amino acids essential for growth. Immediately after the onset of severe amino acid deprivation, in RCstr strains the rate of labelling of RNA by exogenous nucleotide bases was greatly diminished. At first, the initiation of new RNA chains declined faster than the rate of polymerization in RCstr organisms, but as starvation proceeded the rate of polymerization was eventually lowered to about 10% of that found during normal growth. In strain CP79 (RCrel), on the other hand, chain-polymerization rates were unaffected by amino acid withdrawal. Artificial depletion of the intracellular purine nucleotide pools in RCstr or RCrel strains by trimethoprim, before the onset of amino acid deprivation, showed that in the RCstr, but not the RCrel strain, amino acid withdrawal gave rise to an inability of the cells to utilize exogenously supplied purine or pyrimidine bases for RNA synthesis. During a prolonged starvation, the observed 100-fold decrease in the total rate of incorporation of exogenous nucleotide bases into the RNA of RCstr organisms was ascribed to a combination of a tenfold decrease in the overall rate of RNA chain polymerization, at least a fivefold decrease in the ability of the cells to utilize exogenous bases and a preferential inhibition of initiation of stable RNA chains. None of these changes occurred in the corresponding RCrel strain.
机译:在大肠杆菌CP78(RC str )和CP79(RC rel )多氨基酸营养缺陷型(缺少四个氨基酸)中测量了各种RNA组分新形成的链的聚合速率。对增长至关重要。在严重的氨基酸剥夺开始后,立即在RC str 菌株中外源核苷酸碱基对RNA的标记率大大降低。首先,新RNA链的起始下降速度快于RC str 生物的聚合速率,但是随着饥饿的进行,聚合速率最终降低到正常生长过程中的约10%。另一方面,在CP79菌株(RC rel )中,链聚合速率不受氨基酸撤除的影响。在氨基酸剥夺开始之前,甲氧苄啶对RC str 或RC rel 菌株中的细胞内嘌呤核苷酸池进行了人工耗竭,这表明RC str < / sup>,而不是RC rel 菌株,氨基酸撤离导致细胞无法利用外源提供的嘌呤或嘧啶碱基进行RNA合成。在长期饥饿中,观察到的外源核苷酸碱基掺入RC str 生物的RNA的总速率下降了100倍,这归因于RNA总体速率下降了10倍链聚合,细胞利用外源碱基的能力至少降低了五倍,并且优先抑制了稳定RNA链的启动。这些变化均未在相应的RC rel 菌株中发生。

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