Abstract
Isolation and characterization of mutants of Escherichia coli that beta-oxidize fatty acids at normal rates, but which divide very slowly when grown on fatty acids, are described. These mutants grow normally on other carbon sources. By growth on oleate, experiments with radioactive precursors showed that the rates of incorporation into ribonucleic acid, protein, and cell wall were comparable to those observed with the parent, whereas the rate of incorporation into phospholipids was slightly decreased. Under these conditions the rate of incorporation of 32P-orthophosphate into deoxyribonucleic acid was low. On the other hand, by growth on oleate, neither gross mass increase in the different macromolecules nor loss of viability was observed, whereas in the presence of inducer the derepression of the lac operon enzymes occurred. Therefore, extensive turnover of the macromolecules is involved when these mutants are grown on fatty acids. Studies of the crypticity and of the binding of 1-anilino-8-naphthalene sulfonate show differences in membrane structure between the mutants and the constitutive parent. Properties of these mutants, which are affected in the process of cellular division, are discussed.
Full text
PDF











Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Cronan J. E., Jr, Ray T. K., Vagelos P. R. Selection and characterization of an E. coli mutant defective in membrane lipid biosynthesis. Proc Natl Acad Sci U S A. 1970 Mar;65(3):737–744. doi: 10.1073/pnas.65.3.737. [DOI] [PMC free article] [PubMed] [Google Scholar]
- DAVIS B. D., MINGIOLI E. S. Mutants of Escherichia coli requiring methionine or vitamin B12. J Bacteriol. 1950 Jul;60(1):17–28. doi: 10.1128/jb.60.1.17-28.1950. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hsu C. C., Fox C. F. Induction of the lactose transport system in a lipid-synthesis-defective mutant of Escherichia coli. J Bacteriol. 1970 Aug;103(2):410–416. doi: 10.1128/jb.103.2.410-416.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Klein K., Steinberg R., Fiethen B., Overath P. Fatty acid degradation in Escherichia coli. An inducible system for the uptake of fatty acids and further characterization of old mutants. Eur J Biochem. 1971 Apr;19(3):442–450. doi: 10.1111/j.1432-1033.1971.tb01334.x. [DOI] [PubMed] [Google Scholar]
- LENNOX E. S. Transduction of linked genetic characters of the host by bacteriophage P1. Virology. 1955 Jul;1(2):190–206. doi: 10.1016/0042-6822(55)90016-7. [DOI] [PubMed] [Google Scholar]
- LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
- Lazdunski C., Shapiro B. M. Isolation and some properties of cell envelope altered mutants of Escherichia coli. J Bacteriol. 1972 Aug;111(2):495–498. doi: 10.1128/jb.111.2.495-498.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
- MONOD J., COHEN-BAZIRE G., COHN M. Sur la biosynthèse de la beta-galactosidase (lactase) chez Escherichia coli; la spécificité de l'induction. Biochim Biophys Acta. 1951 Nov;7(4):585–599. doi: 10.1016/0006-3002(51)90072-8. [DOI] [PubMed] [Google Scholar]
- McClure W. O., Edelman G. M. Fluorescent probes for conformational states of proteins. I. Mechanism of fluorescence of 2-p-toluidinylnaphthalene-6-sulfonate, a hydrophobic probe. Biochemistry. 1966 Jun;5(6):1908–1919. doi: 10.1021/bi00870a018. [DOI] [PubMed] [Google Scholar]
- Moses R. E., Richardson C. C. Replication and repair of DNA in cells of Escherichia coli treated with toluene. Proc Natl Acad Sci U S A. 1970 Oct;67(2):674–681. doi: 10.1073/pnas.67.2.674. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Overath P., Pauli G., Schairer H. U. Fatty acid degradation in Escherichia coli. An inducible acyl-CoA synthetase, the mapping of old-mutations, and the isolation of regulatory mutants. Eur J Biochem. 1969 Feb;7(4):559–574. [PubMed] [Google Scholar]
- Overath P., Raufuss E. M. The induction of the enzymes of fatty acid degradation in Escherichia coli. Biochem Biophys Res Commun. 1967 Oct 11;29(1):28–33. doi: 10.1016/0006-291x(67)90535-9. [DOI] [PubMed] [Google Scholar]
- ROODYN D. B., MANDEL H. G. A simple membrane fractionation method for determining the distribution of radioactivity in chemical fractions of Bacillus cereus. Biochim Biophys Acta. 1960 Jun 17;41:80–88. doi: 10.1016/0006-3002(60)90371-1. [DOI] [PubMed] [Google Scholar]
- Samuel D., Ailhaud G. Comparative aspects of fatty acid activation in Escherichia coli and Clostridium butyricum. FEBS Lett. 1969 Feb;2(4):213–216. doi: 10.1016/0014-5793(69)80022-0. [DOI] [PubMed] [Google Scholar]
- Schwarz U., Asmus A., Frank H. Autolytic enzymes and cell division of Escherichia coli. J Mol Biol. 1969 May 14;41(3):419–429. doi: 10.1016/0022-2836(69)90285-x. [DOI] [PubMed] [Google Scholar]
- Shapiro B. M., Siccardi A. G., Hirota Y., Jacob F. On the process of cellular division in Escherichia coli. Membrane prtein alterations associated with mutations affecting the initiation of DNA synthesis. J Mol Biol. 1970 Aug 28;52(1):75–89. doi: 10.1016/0022-2836(70)90178-6. [DOI] [PubMed] [Google Scholar]
- TZUR R., SHAPIRO B. DEPENDENCE OF MICROSOMAL LIPID SYNTHESIS ON ADDED PROTEIN. J Lipid Res. 1964 Oct;5:542–547. [PubMed] [Google Scholar]
- Taketa K., Pogell B. M. The effect of palmityl coenzyme A on glucose 6-phosphate dehydrogenase and other enzymes. J Biol Chem. 1966 Feb 10;241(3):720–726. [PubMed] [Google Scholar]
- Weeks G., Shapiro M., Burns R. O., Wakil S. J. Control of fatty acid metabolism. I. Induction of the enzymes of fatty acid oxidation in Escherichia coli. J Bacteriol. 1969 Feb;97(2):827–836. doi: 10.1128/jb.97.2.827-836.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
