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Differential expression of gap and pgk genes within the gap operon of Zymomonas mobilis
- Source :
- Journal of bacteriology. 171(12)
- Publication Year :
- 1989
-
Abstract
- In Zymomonas mobilis, the genes encoding glyceraldehyde-3-phosphate dehydrogenase (GAP) and phosphoglycerate kinase (PGK) are encoded in an operon that is transcribed from tandem promoters. The promoter-proximal gap gene is expressed at six- to ninefold higher levels than the pgk gene from chromosomal genes and from multiple copies of plasmid-borne genes. Two dominant transcripts were identified. The smaller, most abundant transcript contained primarily the gap message, whereas the larger, less abundant message contained both genes. The ratio of message levels for gap and pgk was calculated to be 5:1 and is sufficient to account for the observed differences in levels of GAP and PGK. The differences in message abundance are proposed to result from either transcriptional attenuation or preferential degradation of the 3' region encoding pgk. Increases in gene dosage were accompanied by one-third the expected increase in enzymatic activity on the basis of estimates of copy number, consistent with the presence of a limiting, positive regulatory factor. However, GAP and PGK expressions were not reduced from the chromosome in recombinants that contained multiple copies of the gap operon with inactive genes.
- Subjects :
- Transcription, Genetic
Operon
Restriction Mapping
Gene Expression
Biology
Microbiology
Gene dosage
Plasmid
Escherichia coli
Transcriptional attenuation
RNA, Messenger
Cloning, Molecular
Molecular Biology
Gene
Gap gene
Genetics
Phosphoglycerate kinase
Bacteria
Ethanol
Glyceraldehyde-3-Phosphate Dehydrogenases
Nucleic Acid Hybridization
Promoter
Molecular biology
Blotting, Southern
Phosphoglycerate Kinase
Genes, Bacterial
Multigene Family
Glycolysis
Plasmids
Research Article
Subjects
Details
- ISSN :
- 00219193
- Volume :
- 171
- Issue :
- 12
- Database :
- OpenAIRE
- Journal :
- Journal of bacteriology
- Accession number :
- edsair.doi.dedup.....dba013bee1bdbb237ed924547e5fe2da