Abstract
The expression of the glyoxylate shunt enzymes is required for growth of Escherichia coli on acetate or fatty acids as a sole carbon source. The genes for the two unique enzymes of the glyoxylate shunt, aceA and aceB, are located at 90 min on the E. coli K-12 genetic map. Polar mutations in the aceB gene eliminate aceA gene function, suggesting that these genes constitute an operon and the direction of transcription is from aceB to aceA. Mu d (Ap lac) fusions with the aceA gene have been constructed to study the regulation of the ace operon. Expression of the ace operon is under the transcriptional control of two genes: the iclR gene, which maps near the ace operon, and the fadR gene, which maps at 25 min, and is also involved in the regulation of the fatty acid degradation (fad) regulon. Merodiploid studies demonstrated that both the iclR and fadR genes regulate the glyoxylate shunt in a trans-dominant manner.
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Selected References
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- Bachmann B. J., Low K. B. Linkage map of Escherichia coli K-12, edition 6. Microbiol Rev. 1980 Mar;44(1):1–56. doi: 10.1128/mr.44.1.1-56.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brice C. B., Kornberg H. L. Genetic control of isocitrate lyase activity in Escherichia coli. J Bacteriol. 1968 Dec;96(6):2185–2186. doi: 10.1128/jb.96.6.2185-2186.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Casadaban M. J., Cohen S. N. Lactose genes fused to exogenous promoters in one step using a Mu-lac bacteriophage: in vivo probe for transcriptional control sequences. Proc Natl Acad Sci U S A. 1979 Sep;76(9):4530–4533. doi: 10.1073/pnas.76.9.4530. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kleckner N., Roth J., Botstein D. Genetic engineering in vivo using translocatable drug-resistance elements. New methods in bacterial genetics. J Mol Biol. 1977 Oct 15;116(1):125–159. doi: 10.1016/0022-2836(77)90123-1. [DOI] [PubMed] [Google Scholar]
- Lakshmi T. M., Helling R. B. Acetate metabolism in Escherichia coli. Can J Microbiol. 1978 Feb;24(2):149–153. doi: 10.1139/m78-027. [DOI] [PubMed] [Google Scholar]
- Low K. B. Escherichia coli K-12 F-prime factors, old and new. Bacteriol Rev. 1972 Dec;36(4):587–607. doi: 10.1128/br.36.4.587-607.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lowry O. H., Carter J., Ward J. B., Glaser L. The effect of carbon and nitrogen sources on the level of metabolic intermediates in Escherichia coli. J Biol Chem. 1971 Nov;246(21):6511–6521. [PubMed] [Google Scholar]
- MUNKRES K. D., RICHARDS F. M. THE PURIFICATION AND PROPERTIES OF NEUROSPORA MALATE DEHYDROGENASE. Arch Biochem Biophys. 1965 Mar;109:466–479. doi: 10.1016/0003-9861(65)90391-7. [DOI] [PubMed] [Google Scholar]
- Maloy S. R., Bohlander M., Nunn W. D. Elevated levels of glyoxylate shunt enzymes in Escherichia coli strains constitutive for fatty acid degradation. J Bacteriol. 1980 Aug;143(2):720–725. doi: 10.1128/jb.143.2.720-725.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Maloy S. R., Nunn W. D. Role of gene fadR in Escherichia coli acetate metabolism. J Bacteriol. 1981 Oct;148(1):83–90. doi: 10.1128/jb.148.1.83-90.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Maloy S. R., Nunn W. D. Selection for loss of tetracycline resistance by Escherichia coli. J Bacteriol. 1981 Feb;145(2):1110–1111. doi: 10.1128/jb.145.2.1110-1111.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McEntee K. Genetic analysis of the Escherichia coli K-12 srl region. J Bacteriol. 1977 Dec;132(3):904–911. doi: 10.1128/jb.132.3.904-911.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nunn W. D., Simons R. W., Egan P. A., Maloy S. R. Kinetics of the utilization of medium and long chain fatty acids by mutant of Escherichia coli defective in the fadL gene. J Biol Chem. 1979 Sep 25;254(18):9130–9134. [PubMed] [Google Scholar]
- Pauli G., Overath P. ato Operon: a highly inducible system for acetoacetate and butyrate degradation in Escherichia coli. Eur J Biochem. 1972 Sep 25;29(3):553–562. doi: 10.1111/j.1432-1033.1972.tb02021.x. [DOI] [PubMed] [Google Scholar]
- Simons R. W., Egan P. A., Chute H. T., Nunn W. D. Regulation of fatty acid degradation in Escherichia coli: isolation and characterization of strains bearing insertion and temperature-sensitive mutations in gene fadR. J Bacteriol. 1980 May;142(2):621–632. doi: 10.1128/jb.142.2.621-632.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Simons R. W., Hughes K. T., Nunn W. D. Regulation of fatty acid degradation in Escherichia coli: dominance studies with strains merodiploid in gene fadR. J Bacteriol. 1980 Aug;143(2):726–730. doi: 10.1128/jb.143.2.726-730.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
- VANDERWINKEL E., LIARD P., RAMOS F., WIAME J. M. Genetic control of the regulation of isocitritase and malate synthase in Escherichia coli K 12. Biochem Biophys Res Commun. 1963 Jul 18;12:157–162. doi: 10.1016/0006-291x(63)90254-7. [DOI] [PubMed] [Google Scholar]
- VOGEL H. J., BONNER D. M. Acetylornithinase of Escherichia coli: partial purification and some properties. J Biol Chem. 1956 Jan;218(1):97–106. [PubMed] [Google Scholar]
- Vanderwinkel E., De Vlieghere M. Physiologie et génétique de l'isocitritase et des malate synthases chez Escherichia coli. Eur J Biochem. 1968 Jun;5(1):81–90. doi: 10.1111/j.1432-1033.1968.tb00340.x. [DOI] [PubMed] [Google Scholar]
- Vinopal R. T., Fraenkel D. G. Phenotypic suppression of phosphofructokinase mutations in Escherichia coli by constitutive expression of the glyoxylate shunt. J Bacteriol. 1974 Jun;118(3):1090–1100. doi: 10.1128/jb.118.3.1090-1100.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wegener W. S., Furmanski P., Ajl S. J. Selection of mutants constitutive for several glyoxylate condensing enzymes during growth on valeric acid. Biochim Biophys Acta. 1967 Aug 8;144(1):34–50. [PubMed] [Google Scholar]
