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Ribonucleic Acid and Protein Synthesis During Germination of Myxococcus xanthus Myxospores

机译:粘线球菌粘孢萌发过程中的核糖核酸和蛋白质合成

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摘要

Ribonucleic acid (RNA) and protein synthesis during myxospore germination were examined. When RNA synthesis was inhibited more than 90% by either actinomycin D (Act D) or rifampin, germination was prevented. The data were consistent with the interpretation that rifampin did not interfere with protein synthesis in any way other than by inhibition of messenger RNA formation. Act D concentrations as high as 20 μg/ml did not totally inhibit RNA synthesis. In the presence of 8 μg of Act D/ml, germinating myxospores synthesized transfer RNA, 16S RNA, and 23S RNA. Evidence was presented which indicated that messenger RNA was also synthesized early in the germination period both in the presence and absence of 8 μg of Act D/ml. One explanation for the escape synthesis of RNA in germinating myxospores is that Act D exerts a differential effect on the transcription of larger versus smaller cistrons, the latter having a lower probability of binding Act D. We have found that in the presence of 8 μg of Act D/ml, escape RNA synthesis in myxospores was 25% for 23S RNA, 55% for 16S RNA, and more than 90% for 4S RNA. We have shown that germination of myxospores requires both RNA and protein synthesis during the first 25 to 35 min in germination medium. This finding does not support the earlier suggestion by Ramsey and Dworkin that a stable germination messenger RNA is required for germination of the myxospores of Myxococcus xanthus.
机译:检查了粘孢子萌发过程中的核糖核酸(RNA)和蛋白质合成。当放线菌素D(Act D)或利福平抑制RNA合成超过90%时,发芽被阻止。数据与利福平除了抑制信使RNA形成外不以任何方式干扰蛋白质合成的解释一致。 Act D浓度高达20μg/ ml不能完全抑制RNA合成。在存在8μgAct D / ml的情况下,发芽的粘孢子合成了转移RNA,16S RNA和23S RNA。提出的证据表明,在存在和不存在8μgAct D / ml的情况下,信使RNA也在萌发期的早期合成。 RNA在发芽的粘孢子中逃逸合成的一种解释是,Act D对较大的顺反子和较小的顺反子的转录具有不同的作用,而顺反子的结合概率较低。我们发现存在8μg的顺反子D / ml,粘孢子中的逃逸RNA合成对于23S RNA是25%,对于16S RNA是55%,对于4S RNA是超过90%。我们已经显示,在萌发培养基中的最初25到35分钟内,粘孢子的萌发需要RNA和蛋白质合成。该发现不支持Ramsey和Dworkin的早期建议,即需要稳定的发芽信使RNA才能使黄色粘球菌的粘孢子萌发。

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