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产气气杆菌的镁缺乏。II. 核酸合成速率及其测量方法。

Magnesium starvation of Aerobacter aerogenes. II. Rates of nucleic acid synthesis and methods for their measurement.

作者信息

Kennell D, Kotoulas A

出版信息

J Bacteriol. 1967 Jan;93(1):345-56. doi: 10.1128/jb.93.1.345-356.1967.

Abstract

The rates of synthesis of Aerobacter aerogenes nucleic acids were estimated during incubation of the bacteria in a Mg(++)-free medium. Deoxyribonucleic acid (DNA) synthesized during Mg(++) starvation, or in the preceding exponential growth, remained acid-precipitable for 2.5 hr before breaking down to acid-soluble products during a period of many hours. Rates of DNA synthesis were calculated by correcting the net amounts of DNA per milliliter to values that would have appeared had there been no decay. After the first few hours, this rate was constant, the amount of DNA present at the start of Mg(++) starvation being synthesized every 130 min. Rates of synthesis of total ribonucleic acid (RNA) were established in two ways: (i) by measurements of the incorporation of exogeneous uracil and glucose carbon into RNA, and (ii) by the accumulation of transfer RNA (tRNA), since this component is stable during Mg(++) starvation. After the first few hours, this rate was constant, the amount of RNA present at the start of Mg(++) starvation being synthesized about every 120 min. Fractionation by gradient centrifugation revealed that at all times of starvation the ratio of newly synthesized tRNA-rRNA was the same as it was during exponential growth. Furthermore, newly synthesized ribosomal RNA (rRNA) became a part of polysomal structures. Thus, in the absence of Mg(++), DNA, tRNA, and rRNA were synthesized in the same relative proportions as during exponential growth, at rates close to one-half the instantaneous rates of synthesis in the bacteria growing exponentially at the start of starvation.

摘要

在无镁(Mg++)培养基中培养产气气杆菌期间,对其核酸合成速率进行了估算。在镁(Mg++)饥饿期间或之前的指数生长期合成的脱氧核糖核酸(DNA),在分解为酸溶性产物之前的数小时内,可酸沉淀2.5小时。DNA合成速率是通过将每毫升DNA的净含量校正为若无降解时本应出现的值来计算的。最初几个小时后,该速率保持恒定,镁(Mg++)饥饿开始时存在的DNA量每130分钟合成一次。总核糖核酸(RNA)的合成速率通过两种方式确定:(i)通过测量外源尿嘧啶和葡萄糖碳掺入RNA的情况,以及(ii)通过转运RNA(tRNA)的积累,因为该组分在镁(Mg++)饥饿期间是稳定的。最初几个小时后,该速率保持恒定,镁(Mg++)饥饿开始时存在的RNA量大约每120分钟合成一次。通过梯度离心分级分离表明,在饥饿的所有时间里,新合成的tRNA-rRNA比例与指数生长期相同。此外,新合成的核糖体RNA(rRNA)成为多核糖体结构的一部分。因此,在无镁(Mg++)的情况下,DNA、tRNA和rRNA以与指数生长期相同的相对比例合成,其速率接近饥饿开始时指数生长细菌瞬时合成速率的一半。

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