RNase G-Dependent Degradation of the eno mRNA Encoding a Glycolysis Enzyme Enolase in Escherichia coli(Microbiology & Fermentation Technology)
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概要
- 論文の詳細を見る
Escherichia coli RNase G, encoded by the rng gene, is involved in the processing of 16S rRNA and degradation of the adhE mRNA encoding a fermentative alcohol dehydrogenase. In a search for the intracellular target RNAs of RNase G other than the 16S rRNA precursor and adhE mRNA, total cellular proteins from rng^+ and rng::cat cells were compared by two-dimensional gel electrophoresis. The amount of enolase encoded by the eno gene reproducibly increased two- to three-fold in the rng::cat mutant strain compared with the rng^+ parent strain. Rifampicin chase experiments showed that the half-life of the eno mRNA was some 3 times longer in the rng::cat mutant than in the wild type. These results indicate that the eno mRNA was a substrate of RNase G in vivo, in addition to 16S rRNA precursor and adhE mRNA.
- 社団法人日本農芸化学会の論文
- 2002-10-23
著者
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Wachi Masaaki
Department of Bioengineering, Tokyo Institute of Technology
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NAGAI Kazuo
Department of Bioengineering, Tokyo Institute of Technology
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Nagai K
Yamanouchi Pharmaceutical Co. Ltd. Tokyo Jpn
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Nagai Kazuo
Department Of Applied Biological Chemistry Chubu University
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Nagai K
Chubu Univ. Aichi Jpn
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Kaga Naoko
Department Of Bioengineering Tokyo Institute Of Technology
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Wachi M
Dep. Of Bioengineering Tokyo Inst. Of Technol.
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Wachi Masaaki
Dep. Of Bioengineering Tokyo Inst. Of Technol.
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Wachi Masaaki
Department Of Bioengineering Graduate School Of Bioscience And Biotechnology Tokyo Institute Of Tech
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UMITSUKI Genryou
Noda Institute for Scientific Research
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Umitsuki Genryou
Research And Development Division Kikkoman Corporation
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