Henner D J, Steinberg W
J Bacteriol. 1979 Nov;140(2):555-66. doi: 10.1128/jb.140.2.555-566.1979.
The synthesis of transfer ribonucleic acid (tRNA) was examined during spore formation and spore outgrowth in Bacillus subtilis by two-dimensional polyacrylamide gel electrophoresis of in vivo 32P-labeled RNA. The two-dimensional gel system separated the B. subtilis tRNA's into 32 well-resolved spots, with the relative abundances ranging from 0.9 to 17% of the total. There were several spots (five to six) resolved which were not quantitated due to their low abundance. All of the tRNA species resolved by this gel system were synthesized at every stage examined, including vegetative growth, different stages of sporulation, and different stages of outgrowth. Quantitation of the separated tRNA's showed that in general the tRNA species were present in approximately the same relative abundances at the different developmental periods. tRNA turnover and compartmentation occurring during sporulation were examined by labeling during vegetative growth followed by the addition of excess phosphate to block further 32P incorporation. The two-dimensional gels of these samples showed the same tRNA's seen during vegetative growth, and they were in approximately the same relative abundances, indicating minimal differences in the rates of turnover of individual tRNA's. Vegetatively labeled samples, chased with excess phosphate into mature spores, also showed all of the tRNA species seen during vegetative growth, but an additional five to six minor spots were also observed. These are hypothesized to arise from the loss of 3'-terminal residues from preexisting tRNA's.
通过对体内32P标记RNA进行二维聚丙烯酰胺凝胶电泳,研究了枯草芽孢杆菌孢子形成和孢子萌发过程中转录核糖核酸(tRNA)的合成。二维凝胶系统将枯草芽孢杆菌的tRNA分离成32个分辨率良好的斑点,其相对丰度占总量的0.9%至17%。有几个斑点(五到六个)由于丰度低而未进行定量分析。该凝胶系统分辨出的所有tRNA种类在每个检测阶段均有合成,包括营养生长、孢子形成的不同阶段以及萌发的不同阶段。对分离出的tRNA进行定量分析表明,一般来说,tRNA种类在不同发育时期的相对丰度大致相同。通过在营养生长期间进行标记,然后添加过量磷酸盐以阻止进一步的32P掺入,研究了孢子形成过程中tRNA的周转和区室化。这些样品的二维凝胶显示出与营养生长期间相同的tRNA,且它们的相对丰度大致相同,表明各个tRNA的周转率差异极小。用过量磷酸盐追踪到成熟孢子中的营养标记样品,也显示出营养生长期间所见的所有tRNA种类,但还观察到另外五到六个小斑点。据推测,这些小斑点是由现有tRNA的3'-末端残基丢失产生的。