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!align=left |Citation | |||
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'''No author listed''' (1993) Relative expression of the products of glyoxylate bypass operon: contributions of transcription and translation. ''J. Bacteriol.'' '''175''':4572-5 | |||
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!align=left |Abstract | |||
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Although the genes of the aceBAK operon are expressed from the same promoter, the relative cellular levels of their products are approximately 0.3:1:0.003. Gene and operon fusions with lacZ were constructed to characterize this differential expression. The upshift in expression between aceB and aceA resulted from differences in translational efficiency. In contrast, inefficient translation and premature transcriptional termination contributed to the downshift in expression between aceA and aceK. Premature transcriptional termination occurred within aceK and appears to result from inefficient translation. Deletion of repetitive extragenic palindromic elements between aceA and aceK had little effect on the relative expression of these genes. Rather, the sequences responsible for inefficient expression of aceK lie within the aceK ribosome binding site. | |||
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!align=left |Links | |||
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[http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=8331088 PubMed] [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC204903 PMC204903] | |||
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| | !align=left |Keywords | ||
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|- | Base Sequence; Binding Sites; Escherichia coli/genetics; Escherichia coli/metabolism; Gene Expression; Genes, Bacterial; Glyoxylates/metabolism; Isocitrate Lyase/biosynthesis; Isocitrate Lyase/genetics; Isocitrate Lyase/metabolism; Kinetics; Malate Synthase/biosynthesis; Malate Synthase/genetics; Malate Synthase/metabolism; Molecular Sequence Data; Oligodeoxyribonucleotides; Operon; Promoter Regions, Genetic; Protein Biosynthesis; Protein-Serine-Threonine Kinases/biosynthesis; Protein-Serine-Threonine Kinases/genetics; Protein-Serine-Threonine Kinases/metabolism; Recombinant Fusion Proteins/metabolism; Ribosomes/metabolism; Transcription, Genetic; beta-Galactosidase/genetics; beta-Galactosidase/metabolism | ||
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==Significance {{HelpIcon|Help:Literature}} == | ==Significance {{HelpIcon|Help:Literature}} == | ||
{{LitSignificance}} | {{LitSignificance}} | ||
Revision as of 19:45, 1 September 2013
| Citation |
No author listed (1993) Relative expression of the products of glyoxylate bypass operon: contributions of transcription and translation. J. Bacteriol. 175:4572-5 |
|---|---|
| Abstract |
Although the genes of the aceBAK operon are expressed from the same promoter, the relative cellular levels of their products are approximately 0.3:1:0.003. Gene and operon fusions with lacZ were constructed to characterize this differential expression. The upshift in expression between aceB and aceA resulted from differences in translational efficiency. In contrast, inefficient translation and premature transcriptional termination contributed to the downshift in expression between aceA and aceK. Premature transcriptional termination occurred within aceK and appears to result from inefficient translation. Deletion of repetitive extragenic palindromic elements between aceA and aceK had little effect on the relative expression of these genes. Rather, the sequences responsible for inefficient expression of aceK lie within the aceK ribosome binding site. |
| Links | |
| Keywords |
Base Sequence; Binding Sites; Escherichia coli/genetics; Escherichia coli/metabolism; Gene Expression; Genes, Bacterial; Glyoxylates/metabolism; Isocitrate Lyase/biosynthesis; Isocitrate Lyase/genetics; Isocitrate Lyase/metabolism; Kinetics; Malate Synthase/biosynthesis; Malate Synthase/genetics; Malate Synthase/metabolism; Molecular Sequence Data; Oligodeoxyribonucleotides; Operon; Promoter Regions, Genetic; Protein Biosynthesis; Protein-Serine-Threonine Kinases/biosynthesis; Protein-Serine-Threonine Kinases/genetics; Protein-Serine-Threonine Kinases/metabolism; Recombinant Fusion Proteins/metabolism; Ribosomes/metabolism; Transcription, Genetic; beta-Galactosidase/genetics; beta-Galactosidase/metabolism |
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Annotations
| Gene product | Qualifier | GO ID | GO term name | Evidence Code | with/from | Aspect | Notes | Status |
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