Summary
E. coli wild type bacteria display sensitivity towards serine. A selection medium is described which allows selection of serine resistant mutants. One such mutant is described which presents pleiotropic alterations: it exhibits a thermosensitive growth pattern, alteration in the metabolism of the pppGpp and ppGpp nucleotides, cAMP intracellular level alteration, extreme sensitivity to 2-ketobutyric acid and a defect in the phosphotransferases permeation system. A conjecture explaining these apparently unrelated defects supposes that serine metabolism interferes via phosphoenol pyruvate with a cytoplasmic control of membrane activity (the mutant would be defective in the coupling between membrane and the protein responsible for its cytoplasmic control) and that 2-ketobutyrate is an effector of this activity.
Similar content being viewed by others
Abbreviations
- smg:
-
serine+methionine+glycine (addition to the growth medium)
- IPTG:
-
isopropyl-β-D thiogalactoside (lactose operon inducer)
References
Alföldi, L., Kerekes, E.: Neutralization of the amino acid sensitivity of RCrel Escherichia coli. Biochim. Biophys. Acta 91, 155–157 (1964)
Bachmann, B.J., Low, K.B., Taylor, A.L.: Recalibrated linkage map of Escherichia coli K12. Bacteriol. Rev. 40, 116–167 (1976)
Boer, H.A. De, Bakker, A.J., Weyer, W.J., Gruber, M.: The role of energy generating processes in the degradation of guanosine tetraphosphate, ppGpp, in Escherichia coli. Biochim. Biophys. Acta 432, 361–368 (1976)
Cashel, M.: The control of ribonucleic acid synthesis in Escherichia coli. IV. Relevance of unusual phosphorylated compounds from aminoacid starved stringent strains. J. Biol. Chem. 244, 3133–3141 (1969)
Chao, L.: Gene expression in stringent and relaxed strains of Escherichia coli during aminoacid starvation. Biochem. Biophys. Res. Commun. 77, 42–49 (1977)
Clarke, L., Carbon, J.: A colony bank containing synthetic Col E1 hybrid plasmids representative of the entire E. coli genome. Cell 9, 91–99 (1976)
Danchin, A.: A new technique for selection of sensitive and auxotrophic mutants of E. coli: isolation of a strain sensitive to an excess of one carbon metabolites. Mol. Gen. Genet. 150, 293–299 (1977)
Danchin, A.: Is a metabolic control for the doubling of the macromolecule synthesizing machinery possible? Biochimie 61, 45–50
Fiil, N.P., Willumsen, B.M., Friesen, J.D., Von Meyerburg, K.: Interaction of alleles of the relA, relC and spoT genes in E. coli: analysis of the interconversion of GTP, ppGpp and pppGpp. Mol. Gen. Genet. 150, 87–101 (1977)
Gallant, J., Palmer, L., Pao, C.C.: Anamalous synthesis of ppGpp in growing cells. Cell 11, 181–185 (1977)
Grodzicker, T., Arditti, R.R., Eisen, H.: Establishment of repression by lambdoid phage in catabolite achivator protein and adenylate cyclase mutants of Escherichia coli. Proc. Natl. Acad. Sci. U.S.A. 69, 366–370 (1972)
Hansen, M.T., Pato, M.L., Molin, S., Fiil, N.P., Meyenburg, K. Von: Simple downshifts and resulting lack of correlation between ppGpp pool size and ribonucleic acid accumulation. J. Bacteriol. 122, 585–591 (1975)
Ishiguro, E.E., Ramey, W.D.: Involvment of the relA gene product and feedback inhibition in the regulation of UDP-N-Acetylmuramyl peptide synthesis in Escherichia coli. J. Bacteriol. 135, 766–774 (1978)
Isono, K., Kitakawa, M.: Cluster of ribosomal protein genes in Escherichia coli containing genes for proteins S6, S18 and L9. Proc. Natl. Acad. Sci. U.S.A. 75, 6163–6167 (1978)
Lazzarini, R., Cashel, M., Gallant, J.: On the regulation of guanosine tetraphosphate levels in stringent and relaxed strains of Escherichia coli. J. Biol. Chem. 246, 4381–4385 (1971)
Low, K.B.: Rapid mapping of conditional and auxotrophic mutations in Escherichia coli K12. J. Bacteriol. 113, 798–812 (1973)
Miller, J.H.: Experiments in molecular genetics. New York: Cold Spring Harbour Laboratory 1974
Pardee, A.B., Jacob, F., Monod, J.: Genetic control and cytoplasmic expression of “inductibility” in the synthesis of β-galactosidase by Escherichia coli. J. Mol. Biol. 1, 165–178 (1959)
Postma, P.W., Roseman, S.: The bacterial phosphoenolpyruvate sugar phosphotransferase system. Biochim. Biophys. Acta 457, 213–257 (1976)
Rhoads, D.B., Epstein, W.: Energy coupling to net K+ transport in Escherichia coli. J. Biol. Chem. 352, 1394–1401 (1977)
Saier, M.H., Jr., Feucht, B.U.: Coordinate regulation of adenylate cyclase and carbohydrate permeases by the phosphoenol pyruvate: sugar phosphotransferase system in Salmonella typhimurium. J. Biol. Chem. 250, 7078–7080 (1975)
Saier, M.H., Jr.: Bacterial phosphoenol pyruvate: sugar phosphotransferase systems: structural, functional and evolutionary interrelationships. Bacteriol. Rev. 41, 856–871 (1977)
Shaw, L., Grau, F., Kaback, H.R., Hang, J.S., Walsh, C.T.: Vinylglycolate resistance in Escherichia coli. J. Bacteriol. 121, 1047–1055 (1975)
Somerville, C.R., Ahmed, A.: Mutants of Escherichia coli defective in the degradation of guanosine 5′ triphosphate 3′ diphosphate (pppGpp). Mol. Gen. Genet. 169, 315–323 (1979)
Wash, C.T., Kaback, H.R.: Vinylglycolic acid: an inactivator of the phosphoenol pyruvate — phosphate transferase system in Escherichia coli. J. Biol. Chem. 248, 5456–5462 (1973)
Winslow, R.M.: A consequence of the rel gene during a glucose to lactate downshift in Escherichia coli. J. Biol. Chem. 246, 4872–4877 (1971)
Uzan, M., Danchin, A.: A rapid test for the relA - mutation in E. coli. Biochem. Biophys. Res. Commun. 69, 751–758 (1976)
Uzan, M., Danchin, A.: Correlation between the serine sensitivity and the derepressibility of the ilv genes in Escherichia coli relA- mutants. Mol. Gen. Genet. 165, 21–30 (1978)
Author information
Authors and Affiliations
Additional information
Communicated by G. O'Donovan
Rights and permissions
About this article
Cite this article
Danchin, A., Dondon, L. Serine sensitivity of Escherichia coli K 12: Partial characterization of a serine resistant mutant that is extremely sensitive to 2-ketobutyrate. Molec. Gen. Genet. 178, 155–164 (1980). https://doi.org/10.1007/BF00267224
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00267224