Cooperativity of stabilized mRNA and enhanced translation activity in the cell-free system

被引:18
作者
Kitaoka, Y
Nishimura, N
Niwano, M
机构
[1] Biotechnology Research Laboratory, Kobe Steel Ltd. 5-5, Kobe 651-22, Takatsuka-dai 1-chome, Nishi-ku
关键词
cell-free protein synthesis; ribosome; mRNA degradation; nucleotide triphosphates;
D O I
10.1016/0168-1656(96)01389-2
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Detailed analysis of cell-free translation, coupled transcription-translation in static conditions and a continuous how system based on E. coli S30 extracts was performed. Degradation of template mRNA was the predominant trigger to terminate the protein synthesis. In a coupled system, mRNA was preserved by repeated transcription whereas the starvation of nucleotide triphosphates led to the termination of protein synthesis in less than 1 h. In the CFCF system, NTP was held at the level of initial concentration and therefore did not arrest the translation for 15 h. The accurate coupling of transcriptional rate and translational rate was also crucial to enhance the efficiency of protein synthesis.
引用
收藏
页码:1 / 8
页数:8
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