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. 1970 Mar;101(3):948–958. doi: 10.1128/jb.101.3.948-958.1970

Properties of the Inducible Hydroxyproline Transport System of Pseudomonas putida

Rosa M Gryder 1, Elijah Adams 1
PMCID: PMC250415  PMID: 5438054

Abstract

Features of the transport system for hydroxyproline in a strain of Pseudomonas putida were studied. A mutant, lacking hydroxyproline-2 epimerase and unable to metabolize hydroxy-l-proline, was shown to transport and accumulate this compound after induction. Both entry and exit rates were examined, and kinetic constants for the reaction were determined. Increasing the induction time from 0.5 to 3 hr increased the entry rate three- to fourfold but had only a small and variable effect on the exit rate. Entry followed saturation kinetics. For hydroxy-l-proline, the Km and Vmax values were found to be 3 × 10−5m and 6 μmoles per g (dry weight) per min, respectively. The Km and Vmax for the epimer allohydroxy-d-proline were 10−3m and 0.1 μmole per g (dry weight) per min. Entry rates into “loaded” and “unloaded” cells were found to be the same. Exit was shown to be first order over the range of internal substrate concentrations measured. Exit rates were measured by several different methods and found to be independent of external substrate concentration. The first-order exit rate constant was computed to be 0.23 min−1. Several metabolic inhibitors were examined for their effect on transport. The inhibitory action of N-ethyl maleimide was shown to be greatly reduced if cells were allowed to accumulate hydroxy-l-proline before exposure to the inhibitor. A number of other amino acids interfered with the transport of hydroxy-l-proline; the greatest effect was produced by l-alanine and l-proline.

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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. Alvarado F. Transport of sugars and amino acids in the intestine: evidence for a common carrier. Science. 1966 Feb 25;151(3713):1010–1013. doi: 10.1126/science.151.3713.1010. [DOI] [PubMed] [Google Scholar]
  3. BARRETT J. T., LARSON A. D., KALLIO R. E. The nature of the adaptive lag of Pseudomonas fluorescens toward citrate. J Bacteriol. 1953 Feb;65(2):187–192. doi: 10.1128/jb.65.2.187-192.1953. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. BIBB W. R., STRAUGHN W. R. INDUCIBLE TRANSPORT SYSTEM FOR CITRULLINE IN STREPTOCOCCUS FAECALIS. J Bacteriol. 1964 Apr;87:815–822. doi: 10.1128/jb.87.4.815-822.1964. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. BRITTEN R. J., McCLURE F. T. The amino acid pool in Escherichia coli. Bacteriol Rev. 1962 Sep;26:292–335. doi: 10.1128/br.26.3.292-335.1962. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. BURROUS S. E., DEMOSS R. D. STUDIES ON TRYPTOPHAN PERMEASE IN ESCHERICHIA COLI. Biochim Biophys Acta. 1963 Aug 6;73:623–637. doi: 10.1016/0006-3002(63)90332-9. [DOI] [PubMed] [Google Scholar]
  7. COHEN G. N., MONOD J. Bacterial permeases. Bacteriol Rev. 1957 Sep;21(3):169–194. doi: 10.1128/br.21.3.169-194.1957. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Fox C. F., Kennedy E. P. Specific labeling and partial purification of the M protein, a component of the beta-galactoside transport system of Escherichia coli. Proc Natl Acad Sci U S A. 1965 Sep;54(3):891–899. doi: 10.1073/pnas.54.3.891. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Gryder R. M., Adams E. Inducible degradation of hydroxyproline in Pseudomonas putida: pathway regulation and hydroxyproline uptake. J Bacteriol. 1969 Jan;97(1):292–306. doi: 10.1128/jb.97.1.292-306.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. HORECKER B. L., THOMAS J., MONOD J. Galactose transport in Escherichia coli. I. General properties as studied in a galactokinaseless mutant. J Biol Chem. 1960 Jun;235:1580–1585. [PubMed] [Google Scholar]
  11. HORECKER B. L., THOMAS J., MONOD J. Galactose transport in Escherichia coli. II. Characteristics of the exit process. J Biol Chem. 1960 Jun;235:1586–1590. [PubMed] [Google Scholar]
  12. Halpern Y. S., Even-Shoshan A. Properties of the glutamate transport system in Escherichia coli. J Bacteriol. 1967 Mar;93(3):1009–1016. doi: 10.1128/jb.93.3.1009-1016.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. INUI Y., AKEDO H. AMINO ACID UPTAKE BY ESCHERICHIA COLI GROWN IN PRESENCE OF AMINO ACIDS. EVIDENCE FOR REPRESSIBILITY OF AMINO ACID UPTAKE. Biochim Biophys Acta. 1965 Jan 25;94:143–152. doi: 10.1016/0926-6585(65)90018-x. [DOI] [PubMed] [Google Scholar]
  14. KOCH A. L. THE ROLE OF PERMEASE IN TRANSPORT. Biochim Biophys Acta. 1964 Jan 27;79:177–200. doi: 10.1016/0926-6577(64)90050-6. [DOI] [PubMed] [Google Scholar]
  15. KOGUT M., PODOSKI E. P. Oxidative pathways in a fluorescent Pseudomonas. Biochem J. 1953 Dec;55(5):800–811. doi: 10.1042/bj0550800. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Lessie T., Neidhardt F. C. Adenosine triphosphate-linked control of Pseudomonas aeruginosa glucose-6-phosphate dehydrogenase. J Bacteriol. 1967 Apr;93(4):1337–1345. doi: 10.1128/jb.93.4.1337-1345.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Lyon R. H., Rogers P., Hall W. H., Lichtein H. C. Inducible glutamate transport in Mycobacteria and its relation to glutamate oxidation. J Bacteriol. 1967 Jul;94(1):92–100. doi: 10.1128/jb.94.1.92-100.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. ROTMAN B., GUZMAN R. Transport of galactose from the inside to the outside of Escherichia coli. Pathol Biol. 1961 Apr;9:806–810. [PubMed] [Google Scholar]
  19. Ring K. Die induktion des aktiven Transportes neutraler Amino-säuren bei Streptomyces hydrogenans. Biochim Biophys Acta. 1969 Jul 15;183(2):375–393. doi: 10.1016/0005-2736(69)90094-7. [DOI] [PubMed] [Google Scholar]
  20. Ruiz-Amil M., Aparicio M. L., Canovas J. L. Regulation of the synthesis of glyceraldehyde-3-phosphate dehydrogenase in Pseudomonas putida. FEBS Lett. 1969 Apr;3(1):65–67. doi: 10.1016/0014-5793(69)80098-0. [DOI] [PubMed] [Google Scholar]
  21. Schwencke J., Magaña-Schwencke N. Derepression of a proline transport system in Saccharomyces chevalieri by nitrogen starvation. Biochim Biophys Acta. 1969 Mar 11;173(2):302–312. doi: 10.1016/0005-2736(69)90113-8. [DOI] [PubMed] [Google Scholar]
  22. Wiley W. R., Matchett W. H. Tryptophan transport in Neurospora crassa. II. Metabolic control. J Bacteriol. 1968 Mar;95(3):959–966. doi: 10.1128/jb.95.3.959-966.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]

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