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. 1980 Aug;143(2):726–730. doi: 10.1128/jb.143.2.726-730.1980

Regulation of fatty acid degradation in Escherichia coli: dominance studies with strains merodiploid in gene fadR.

R W Simons, K T Hughes, W D Nunn
PMCID: PMC294351  PMID: 7009562

Abstract

Strains stably merodiploid in the 25-min region of the chromosome of Escherichia coli were constructed and used in dominance tests between various wild-type and mutant alleles of the fadR gene. Whereas the monoploid fadR+ and fadR strains were inducible and constitutive, respectively, for the enzymes involved in fatty acid degradation (fad), merodiploids with at least one fadR+ allele were inducible. This observation was true whether the fadR+ allele resided on the main chromosome or on the episome. These results show that fadR+ is trans dominant to fadR, and they are consistent with the proposal that the fadR gene product is a repressor protein. Complementation tests were also performed by constructing 24 merodiploids harboring fadR alleles on both the main chromosome and the episome. All of these fadR/fadR diploids were able to utilize the noninducing substrate decanoate as sole carbon source, suggesting that only one polypeptide is encoded by the fadR gene.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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