PMID:8331088: Difference between revisions

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<span style = 'font-size: large'> '''Chung, T, Resnik, E, Stueland, C and LaPorte, DC'''  (1993) Relative expression of the products of glyoxylate bypass operon: contributions of transcription and translation.''J. Bacteriol.'' '''175''':4572-5</span>
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!align=left  |Citation
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'''Chung, T, Resnik, E, Stueland, C and LaPorte, DC'''  (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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[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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|{{TableHeadingColor}} |'''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.
!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
|{{TableHeadingColor}} nowrap |'''Links''' ||  [http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=8331088 PubMed]
 
[http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pubmed&pubmedid=8331088 Full text]
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==Annotations {{HelpIcon|Help:Literature}}==
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!|Gene product!!Qualifier!!GO ID!!GO term name!!Evidence Code!!with/from!!Aspect!!Notes!!Status
 
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==EcoliWiki Links {{HelpIcon|Help:Literature}} ==
==EcoliWiki Links {{HelpIcon|Help:Literature}} ==

Latest revision as of 04:53, 15 September 2013

Citation

Chung, T, Resnik, E, Stueland, C and LaPorte, DC (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

PubMed PMC204903

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

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