Regulation and Over-expression of the fnr Gene of Escherichia coli
- 1 December 1987
- journal article
- research article
- Published by Microbiology Society in Microbiology
- Vol. 133 (12) , 3279-3288
- https://doi.org/10.1099/00221287-133-12-3279
Abstract
The fnr gene of Escherichia coli encodes a transcriptional activator (FNR) which is required for the expression of a number of genes involved in anaerobic respiratory pathways. From the study of a translational fusion of fnr to the gene for .beta.-galactosidase (lacZ) it has been concluded that the fnr gene is expressed under both aerobic and anaerobic conditions and is subject to autoregulation and repression by glucose, particularly during anaerobic growth. These findings imply that during anaerobiosis the FNR protein adopts an active conformation, in which it functions both as a repressor of the fnr gene and as an activator of fnr-dependent genes. Sequences in the 5'' non-coding region of fnr which could be involved in autoregulation are discussed. The fnr coding region was cloned into an expression vector which has allowed an amplification of FNR synthesis such that it accounts for about 2% of total cell protein. The ability to over-produce FNR in this way should be very useful for future biochemical studies.This publication has 23 references indexed in Scilit:
- Amplification and Product Identification of the fnr gene of Escherichia cokiMicrobiology, 1982
- Nucleotide Sequence Coding for the Flavoprotein Subunit of the Fumarate Reductase of Escherichia coliEuropean Journal of Biochemistry, 1982
- A dot-immunobinding assay for monoclonal and other antibodiesAnalytical Biochemistry, 1982
- A reliable method for the recovery of DNA fragments from agarose and acrylamide gelsAnalytical Biochemistry, 1981
- “Western Blotting”: Electrophoretic transfer of proteins from sodium dodecyl sulfate-polyacrylamide gels to unmodified nitrocellulose and radiographic detection with antibody and radioiodinated protein AAnalytical Biochemistry, 1981
- A method for sequencing single-stranded cloned DNA in both directionsBioscience Reports, 1981
- In vitro gene fusions that join an enzymatically active beta-galactosidase segment to amino-terminal fragments of exogenous proteins: Escherichia coli plasmid vectors for the detection and cloning of translational initiation signalsJournal of Bacteriology, 1980
- The Chromosomal Location and Pleiotropic Effects of Mutations of the nirA+ Gene of Escherichia coli k12: The Essential Role of nirA+ in Nitrite Reduction and in Other Anaerobic Redox ReactionsJournal of General Microbiology, 1978
- A mutation leading to the total lack of nitrite reductase activity in Escherichia coli K 12Molecular Genetics and Genomics, 1978
- Mutants of Escherichia coli K12 Unable to use Fumarate as an Anaerobic Electron AcceptorJournal of General Microbiology, 1976