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The Mechanism of the Tyrosine Transporter TyrP Supports a Proton Motive Tyrosine Decarboxylation Pathway in Lactobacillus brevis

Wolken, Wout A. M., Lucas, Patrick M., Lonvaud-Funel, Aline, Lolkema, Juke S.·2006·Journal of Bacteriology

Abstract

The tyrosine decarboxylase operon of Lactobacillus brevis IOEB9809 contains, adjacent to the tyrosine decarboxylase gene, a gene for TyrP, a putative tyrosine transporter. The two genes potentially form a proton motive tyrosine decarboxylation pathway. The putative tyrosine transporter gene of L. brevis was expressed in Lactococcus lactis and functionally characterized using right-side-out membranes. The transporter very efficiently catalyzes homologous tyrosine-tyrosine exchange and heterologous exchange between tyrosine and its decarboxylation product tyramine. Tyrosine-tyramine exchange was shown to be electrogenic. In addition to the exchange mode, the transporter catalyzes tyrosine uniport but at a much lower rate. Analysis of the substrate specificity of the transporter by use of a set of 19 different tyrosine substrate analogues showed that the main interactions between the protein and the substrates involve the amino group and the phenyl ring with the para hydroxyl group. The carboxylate group that is removed in the decarboxylation reaction does not seem to contribute to the affinity of the protein for the substrates significantly. The properties of the TyrP protein are those typical for precursor-product exchangers that operate in proton motive decarboxylation pathways. It is proposed that tyrosine decarboxylation in L. brevis results in proton motive force generation by an indirect proton pumping mechanism.

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Research works printed but not linked: 29

  1. Abe, K., H. Hayashi, and P. C. Maloney. 1996. Exchange of aspartate and alanine. Mechanism for development of a proton-motive force in bacteria. J. Biol. Chem. 271 : 3079-3084. · DOI
  2. 10.1128/JB.184.11.2906-2913.2002 · DOI
  3. Abe, K., Z. S. Ruan, and P. C. Maloney. 1996. Cloning, sequencing, and expression in Escherichia coli of OxlT, the oxalate:formate exchange protein of Oxalobacter formigenes. J. Biol. Chem. 271 : 6789-6793. · DOI
  4. Anantharam, V., M. J. Allison, and P. C. Maloney. 1989. Oxalate:formate exchange. The basis for energy coupling in Oxalobacter. J. Biol. Chem. 264 : 7244-7250. · DOI
  5. Bandell, M., V. Ansanay, N. Rachidi, S. Dequin, and J. S. Lolkema. 1997. Membrane potential generating malate (MleP) and citrate (CitP) transporters of lactic acid bacteria are homologous proteins. Substrate specificity of the 2-hydroxy-carboxylate transporter family. J. Biol. Chem. 272 : 18140-18146. · DOI
  6. Bandell, M., and J. S. Lolkema. 1999. Stereoselectivity of the membrane potential generating citrate (CitP) and malate (MleP) transporters of lactic acid bacteria. Biochemistry 38 : 10352-10360. · DOI
  7. Bandell, M., and J. S. Lolkema. 2000. Arg425 of the citrate transporter CitP is responsible for high affinity binding of di- and tricarboxylates. J. Biol. Chem. 275 : 39130-39136. · DOI
  8. Busch, W., and M. H. Saier, Jr. 2004. The IUBMB-endorsed transporter classification system. Mol. Biotechnol. 27 : 253-262. · DOI
  9. 10.1128/AEM.68.7.3537-3544.2002 · DOI · Paper page
  10. 10.1128/aem.62.10.3662-3667.1996 · DOI
  11. Fernández, M., D. M. Linares, and M. A. Alvarez. 2004. Sequencing of the tyrosine decarboxylase cluster of Lactococcus lactis IPLA 655 and the development of a PCR method for detecting tyrosine decarboxylating lactic acid bacteria. J. Food Prot. 67 : 2521-2529. · DOI
  12. 10.1128/jb.179.10.3362-3364.1997 · DOI
  13. Kuipers, O. P., M. M. Beerthuyzen, R. J. Siezen, and W. M. De Vos. 1993. Characterization of the nisin gene cluster nisABTCIPR of Lactococcus lactis. Requirement of expression of the nisA and nisI genes for development of immunity. Eur. J. Biochem. 216 : 281-291. · DOI
  14. Kunji, E. R., I. Mierau, A. Hagting, B. Poolman, and W. N. Konings. 1996. The proteolytic systems of lactic acid bacteria. Antonie Leeuwenhoek 70 : 187-221. · DOI
  15. Kunji, E. R. S., D. J. Slotboom, and B. Poolman. 2003. Lactococcus lactis as host for overproduction of functional membrane proteins. Biochim. Biophys. Acta 1610 : 97-108. · DOI
  16. Lolkema, J. S., B. Poolman, and W. N. Konings. 1996. Secondary transporters and metabolic energy generation in bacteria, p. 229-260. In W. N. Konings, H. R. Kaback, and J. S. Lolkema (ed.), Handbook of biophysics. Elsevier Science, Amsterdam, The Netherlands.
  17. Lonvaud-Funel, A. 2001. Biogenic amines in wines: role of lactic acid bacteria. FEMS Microbiol. Lett. 199 : 9-13. · DOI · Paper page
  18. Lucas, P., and A. Lonvaud-Funel. 2002. Purification and partial gene sequence of the tyrosine decarboxylase of Lactobacillus brevis IOEB 9809. FEMS Microbiol. Lett. 211 : 85-89. · DOI
  19. Lucas, P., J. Landete, M. Coton, E. Coton, and A. Lonvaud-Funel. 2003. The tyrosine decarboxylase operon of Lactobacillus brevis IOEB 9809: characterization and conservation in tyramine-producing bacteria. FEMS Microbiol. Lett. 229 : 65-71. · DOI · Paper page
  20. 10.1128/AEM.71.3.1417-1424.2005 · DOI
  21. Marty-Teysset, C., J. S. Lolkema, P. Schmitt, C. Divies, and W. N. Konings. 1995. Membrane potential generating transport of citrate and malate catalyzed by the citP gene product of Leuconostoc mesenteroides. J. Biol. Chem. 270 : 25370-25376. · DOI
  22. 10.1128/jb.175.10.2864-2870.1993 · DOI
  23. 10.1128/jb.149.2.733-738.1982 · DOI
  24. 10.1128/jb.173.19.6030-6037.1991 · DOI
  25. Silla Santos, M. H. 1996. Biogenic amines: their importance in food. Int. J. Food Microbiol. 29 : 213-231. · DOI · Paper page
  26. 10.1128/MMBR.69.4.665-695.2005 · DOI
  27. Soksawatmaekhin, W., A. Kuraishi, K. Sakata, K. Kashiwagi, and K. Igarashi. 2004. Excretion and uptake of cadaverine by CadB and its physiological functions in Escherichia coli. Mol. Microbiol. 51 : 1401-1412. · DOI
  28. 10.1128/am.29.6.807-813.1975 · DOI · Paper page
  29. 10.1128/jb.177.10.2863-2869.1995 · DOI

Metadata

Authors
Wolken, W. A. M., Lucas, P. M., Lonvaud-Funel, A., & Lolkema, J. S.
Venue
Journal of Bacteriology
Published
2006-03-15
Volume
188
Issue
6
Pages
2198-2206
ISSN
  • 0021-9193
  • 1098-5530
Cited by
84
References
0
Language
en

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CoChat. (2026). Citation check: The Mechanism of the Tyrosine Transporter TyrP Supports a Proton Motive Tyrosine Decarboxylation Pathway in Lactobacillus brevis. https://app.cochat.ai/papers/10.1128/jb.188.6.2198-2206.2006
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Wolken, W. A. M., Lucas, P. M., Lonvaud-Funel, A., & Lolkema, J. S. (2006). The Mechanism of the Tyrosine Transporter TyrP Supports a Proton Motive Tyrosine Decarboxylation Pathway in Lactobacillus brevis. Journal of Bacteriology. https://doi.org/10.1128/jb.188.6.2198-2206.2006

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