Tamura A
J Bacteriol. 1967 Jun;93(6):2009-16. doi: 10.1128/jb.93.6.2009-2016.1967.
In ribonucleic acid (RNA) extracted by phenol and sodium dodecyl sulfate from purified reticulate bodies of meningopneumonitis (MP) organisms, 21S, 16S, and 4S RNA were found by sucrose density gradient sedimentation analysis. When purified reticulate bodies were homogenized by sonic treatment or by treatment with sodium deoxycholate and were fractionated by differential centrifugation, more than 50% of the RNA was recovered in the fraction which was sedimented by centrifugation at 105,000 x g for 2 hr, but not at 13,000 x g for 20 min. From homogenates prepared in this manner, 50S and 30S particles containing RNA were isolated by sucrose density gradient centrifugation. These 50S and 30S particles were also found in lysates of cytoplasmic fractions of infected cells which were labeled by (32)P during 17 to 17.5 hr or 15 to 18 hr after infection. The synthesis of 50S and 30S particles was not inhibited by actinomycin D. When infected cells were homogenized in the presence of 0.01 or 0.02 m MgCl(2), 70S particles were isolated instead of 50S and 30S particles. When dialyzed against low concentrations of MgCl(2), the 70S particles dissociated to 50S and 30S particles. The base ratio of the 70S particles is very similar to that of 16S plus 21S RNA. The characteristics of the 70S, 50S, and 30S particles suggest that these are ribosome particles, similar to bacterial ribosomes.
用苯酚和十二烷基硫酸钠从纯化的脑膜肺炎(MP)病原体网状体中提取的核糖核酸(RNA),通过蔗糖密度梯度沉降分析发现了21S、16S和4S RNA。当通过超声处理或用脱氧胆酸钠处理使纯化的网状体匀浆,并通过差速离心分级分离时,超过50%的RNA在以105,000×g离心2小时沉淀的级分中回收,但在13,000×g离心20分钟时未回收。用这种方法制备的匀浆,通过蔗糖密度梯度离心分离出含有RNA的50S和30S颗粒。在感染后17至17.5小时或15至18小时用(32)P标记的感染细胞胞质级分的裂解物中也发现了这些50S和30S颗粒。50S和30S颗粒的合成不受放线菌素D的抑制。当在0.01或0.02 m MgCl(2)存在下将感染细胞匀浆时,分离出的是70S颗粒而不是50S和30S颗粒。当用低浓度的MgCl(2)透析时,70S颗粒解离为50S和30S颗粒。70S颗粒的碱基比率与16S加21S RNA的碱基比率非常相似。70S、50S和30S颗粒的特征表明,这些是核糖体颗粒,类似于细菌核糖体。