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. 1977 Mar;129(3):1257–1265. doi: 10.1128/jb.129.3.1257-1265.1977

Role of transport systems in amino acid metabolism: leucine toxicity and the branched-chain amino acid transport systems.

S C Quay, T E Dick, D L Oxender
PMCID: PMC235096  PMID: 321421

Abstract

The livR locus, which leads to a trans-recessive derepression of branched-chain amino acid transport and periplasmic branched-chain amino acid-binding proteins, is responsible for greatly increased sensitivity toward growth inhibition by leucine, valine, and serine and, as shown previously, for increased sensitivity toward toxicity by branched-chain amino acid analogues, such as 4-azaleucine or 5',5',5'-trifluoroleucine. These phenotypes are similar to those of relA mutants; however, the livR mutants retain the stringent response of ribonucleic acid synthesis. However, an increase in the rate of transport or in the steady-state intracellular level of amino acids in the livR strain cannot completely account for this sensitivity. The ability of the LIV-I transport system to carry out exchange of pool amino acids for extracellular leucine is a major factor in leucine sensitivity. The previous finding that inhibition of threonine deaminase by leucine contributes to growth inhibition is confirmed by simulating the in vivo conditions using a toluene-treated cell preparation with added amino acids at levels corresponding to the internal pool. The relationship between transport systems and corresponding biosynthetic pathways is discussed and the general principle of a coordination in the regulation of transport and biosynthetic pathways is forwarded. The finding that the LIV-I transport system functions well for amino acid exchange in contrast to the LIV-II system provides another feature that distinguishes these systems in addition to previously described differences in regulation and energetics.

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Selected References

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

  1. AMES G. F. UPTAKE OF AMINO ACIDS BY SALMONELLA TYPHIMURIUM. Arch Biochem Biophys. 1964 Jan;104:1–18. doi: 10.1016/s0003-9861(64)80028-x. [DOI] [PubMed] [Google Scholar]
  2. Anderson J. J., Quay S. C., Oxender D. L. Mapping of two loci affecting the regulation of branched-chain amino acid transport in Escherichia coli K-12. J Bacteriol. 1976 Apr;126(1):80–90. doi: 10.1128/jb.126.1.80-90.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. BOREK E., RYAN A., ROCKENBACH J. Nucleic acid metabolism in relation to the lysogenic phenomenon. J Bacteriol. 1955 Apr;69(4):460–467. doi: 10.1128/jb.69.4.460-467.1955. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Calhoun D. H. Threonine deaminase from Escherichia coli: feedback-hypersensitive enzyme from a genetic regulatory mutant. J Bacteriol. 1976 Apr;126(1):56–63. doi: 10.1128/jb.126.1.56-63.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Cosloy S. D., McFall E. L-Serine-sensitive mutants of Escherichia coli K-12. J Bacteriol. 1970 Sep;103(3):840–841. doi: 10.1128/jb.103.3.840-841.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. De Felice M., Guardiola J., Lamberti A., Iaccarino M. Escherichia coli K-12 mutants altered in the transport systems for oligo- and dipeptides. J Bacteriol. 1973 Nov;116(2):751–756. doi: 10.1128/jb.116.2.751-756.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. De Felice M., Guardiola J., Malorni M. C., Klopotowski T., Iaccarino M. Regulation of the pool size of valine in Escherichia coli K-12. J Bacteriol. 1974 Dec;120(3):1058–1067. doi: 10.1128/jb.120.3.1058-1067.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. EIDLIC L., NEIDHARDT F. C. ROLE OF VALYL-SRNA SYNTHETASE IN ENZYME REPRESSION. Proc Natl Acad Sci U S A. 1965 Mar;53:539–543. doi: 10.1073/pnas.53.3.539. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. FREUNDLICH M., BURNS R. O., UMBARGER H. E. Control of isoleucine, valine, and leucine biosynthesis. I. Multivalent repression. Proc Natl Acad Sci U S A. 1962 Oct 15;48:1804–1808. doi: 10.1073/pnas.48.10.1804. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Fiil N., Friesen J. D. Isolation of "relaxed" mutants of Escherichia coli. J Bacteriol. 1968 Feb;95(2):729–731. doi: 10.1128/jb.95.2.729-731.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. HORVATH I., GADO I. POSSIBLE CAUSES OF LEUCINE INHIBITION IN ESCHERICHIA COLI K-12 GAMMA-28. Acta Microbiol Acad Sci Hung. 1965;12:103–107. [PubMed] [Google Scholar]
  12. Harrison L. I., Christensen H. N., Handlogten M. E., Oxender D. L., Quay S. C. Transport of L-4-azaleucine in Escherichia coli. J Bacteriol. 1975 Jun;122(3):957–965. doi: 10.1128/jb.122.3.957-965.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Jackson J., Williams L. S., Umbarger H. E. Regulation of synthesis of the branched-chain amino acids and cognate aminoacyl-transfer ribonucleic acid synthetases of Escherichia coli: a common regulatory element. J Bacteriol. 1974 Dec;120(3):1380–1386. doi: 10.1128/jb.120.3.1380-1386.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. KJELDGAARD N. O., MAALOE O., SCHAECHTER M. The transition between different physiological states during balanced growth of Salmonella typhimurium. J Gen Microbiol. 1958 Dec;19(3):607–616. doi: 10.1099/00221287-19-3-607. [DOI] [PubMed] [Google Scholar]
  15. Kane J. F. Metabolic interlock: mediation of interpathway regulation by divalent cations. Arch Biochem Biophys. 1975 Oct;170(2):452–460. doi: 10.1016/0003-9861(75)90140-x. [DOI] [PubMed] [Google Scholar]
  16. Kashket E. R., Wong P. T. The intracellular pH of Escherichia coli. Biochim Biophys Acta. 1969 Oct 14;193(1):212–214. doi: 10.1016/0005-2736(69)90074-1. [DOI] [PubMed] [Google Scholar]
  17. LEAVITT R. I., UMBARGER H. E. Isoleucine and valine metabolism in Escherichia coli. XI. Valine inhibition of the growth of Escherichia coli strain K-12. J Bacteriol. 1962 Mar;83:624–630. doi: 10.1128/jb.83.3.624-630.1962. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. 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]
  19. Levinthal M., Williams L. S., Umbarger H. E. Role of threonine deaminase in the regulation of isoleucine and valine biosynthesis. Nat New Biol. 1973 Nov 21;246(151):65–68. doi: 10.1038/newbio246065a0. [DOI] [PubMed] [Google Scholar]
  20. Lin E. C. The genetics of bacterial transport systems. Annu Rev Genet. 1970;4:225–262. doi: 10.1146/annurev.ge.04.120170.001301. [DOI] [PubMed] [Google Scholar]
  21. NEIDHARDT F. C. Properties of a bacterial mutant lacking amino acid control of RNA synthesis. Biochim Biophys Acta. 1963 Mar 26;68:365–379. doi: 10.1016/0006-3002(63)90158-6. [DOI] [PubMed] [Google Scholar]
  22. Neidhardt F. C., Bloch P. L., Smith D. F. Culture medium for enterobacteria. J Bacteriol. 1974 Sep;119(3):736–747. doi: 10.1128/jb.119.3.736-747.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Quay S. C., Kline E. L., Oxender D. L. Role of leucyl-tRNA synthetase in regulation of branched-chain amino-acid transport. Proc Natl Acad Sci U S A. 1975 Oct;72(10):3921–3924. doi: 10.1073/pnas.72.10.3921. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Quay S. C., Oxender D. L. Regulation of branched-chain amino acid transport in Escherichia coli. J Bacteriol. 1976 Sep;127(3):1225–1238. doi: 10.1128/jb.127.3.1225-1238.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Quay S. C., Oxender D. L., Tsuyumu S., Umbarger H. E. Separate regulation of transport and biosynthesis of leucine, isoleucine, and valine in bacteria. J Bacteriol. 1975 Jun;122(3):994–1000. doi: 10.1128/jb.122.3.994-1000.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Rahmanian M., Claus D. R., Oxender D. L. Multiplicity of leucine transport systems in Escherichia coli K-12. J Bacteriol. 1973 Dec;116(3):1258–1266. doi: 10.1128/jb.116.3.1258-1266.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Rogerson A. C., Freundlich M. Control of isoleucine, valine and leucine biosynthesis. 8. Mechanism of growth inhibition by leucine in relaxed and stringent strains of Escherichia coli K-12. Biochim Biophys Acta. 1970 Apr 14;208(1):87–98. doi: 10.1016/0304-4165(70)90051-6. [DOI] [PubMed] [Google Scholar]
  28. Templeton B. A., Savageau M. A. Transport of biosynthetic intermediates: regulation of homoserine and threonine uptake in Escherichia coli. J Bacteriol. 1974 Oct;120(1):114–120. doi: 10.1128/jb.120.1.114-120.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Tomich P. K., Chiu C. S., Wovcha M. G., Greenberg G. R. Evidence for a complex regulating the in vivo activities of early enzymes induced by bacteriophage T4. J Biol Chem. 1974 Dec 10;249(23):7613–7622. [PubMed] [Google Scholar]
  30. Vonder Haar R. A., Umbarger H. E. Isoleucine and valine metabolism in Escherichia coli. XIX. Inhibition of isoleucine biosynthesis by glycyl-leucine. J Bacteriol. 1972 Oct;112(1):142–147. doi: 10.1128/jb.112.1.142-147.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]

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