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. 1997 Feb;179(4):1135–1142. doi: 10.1128/jb.179.4.1135-1142.1997

A conserved glutamate residue, Glu-257, is important for substrate binding and transport by the Escherichia coli mannitol permease.

C A Saraceni-Richards 1, G R Jacobson 1
PMCID: PMC178809  PMID: 9023195

Abstract

The mannitol permease, or D-mannitol-specific enzyme II of the phosphoenolpyruvate-dependent carbohydrate phosphotransferase system (PTS) of Escherichia coli, both transports and phosphorylates its substrate. Previous analyses of the amino acid sequences of PTS permeases specific for various carbohydrates in different species of bacteria revealed several regions of similarity. The most highly conserved region includes a GIXE motif, in which the glutamate residue is completely conserved among the permeases that contain this motif. The corresponding residue in the E. coli mannitol permease is Glu-257, which is located in a large putative cytoplasmic loop of the transmembrane domain of the protein. We used site-directed mutagenesis to investigate the role of Glu-257. The properties of proteins with mutations at position 257 suggest that a carboxylate side chain at this position is essential for mannitol binding. E257A and E257Q mutant proteins did not bind mannitol detectably, while the E257D mutant could still bind this substrate. Kinetic studies with the E257D mutant protein also showed that a glutamate residue at position 257 of this permease is specifically required for efficient mannitol transport. While the E257D permease phosphorylated mannitol with kinetic parameters similar to those of the wild-type protein, the Vmax for mannitol uptake by this mutant protein is less than 5% that of the wild type. These results suggest that Glu-257 of the mannitol permease and the corresponding glutamate residues of other PTS permeases play important roles both in binding the substrate and in transporting it through the membrane.

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Selected References

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  1. Begley G. S., Hansen D. E., Jacobson G. R., Knowles J. R. Stereochemical course of the reactions catalyzed by the bacterial phosphoenolpyruvate:glucose phosphotransferase system. Biochemistry. 1982 Oct 26;21(22):5552–5556. doi: 10.1021/bi00265a026. [DOI] [PubMed] [Google Scholar]
  2. Bradford M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976 May 7;72:248–254. doi: 10.1006/abio.1976.9999. [DOI] [PubMed] [Google Scholar]
  3. Briggs C. E., Khandekar S. S., Jacobson G. R. Structure/function relationships in the Escherichia coli mannitol permease: identification of regions important for membrane insertion, substrate binding and oligomerization. Res Microbiol. 1992 Feb;143(2):139–149. doi: 10.1016/0923-2508(92)90003-7. [DOI] [PubMed] [Google Scholar]
  4. Chen Z. J., Parent L., Maniatis T. Site-specific phosphorylation of IkappaBalpha by a novel ubiquitination-dependent protein kinase activity. Cell. 1996 Mar 22;84(6):853–862. doi: 10.1016/s0092-8674(00)81064-8. [DOI] [PubMed] [Google Scholar]
  5. Deng W. P., Nickoloff J. A. Site-directed mutagenesis of virtually any plasmid by eliminating a unique site. Anal Biochem. 1992 Jan;200(1):81–88. doi: 10.1016/0003-2697(92)90280-k. [DOI] [PubMed] [Google Scholar]
  6. Elferink M. G., Driessen A. J., Robillard G. T. Functional reconstitution of the purified phosphoenolpyruvate-dependent mannitol-specific transport system of Escherichia coli in phospholipid vesicles: coupling between transport and phosphorylation. J Bacteriol. 1990 Dec;172(12):7119–7125. doi: 10.1128/jb.172.12.7119-7125.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Grisafi P. L., Scholle A., Sugiyama J., Briggs C., Jacobson G. R., Lengeler J. W. Deletion mutants of the Escherichia coli K-12 mannitol permease: dissection of transport-phosphorylation, phospho-exchange, and mannitol-binding activities. J Bacteriol. 1989 May;171(5):2719–2727. doi: 10.1128/jb.171.5.2719-2727.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Jacobson G. R. Interrelationships between protein phosphorylation and oligomerization in transport and chemotaxis via the Escherichia coli mannitol phosphotransferase system. Res Microbiol. 1992 Jan;143(1):113–116. doi: 10.1016/0923-2508(92)90040-u. [DOI] [PubMed] [Google Scholar]
  9. Jacobson G. R., Lee C. A., Saier M. H., Jr Purification of the mannitol-specific enzyme II of the Escherichia coli phosphoenolpyruvate:sugar phosphotransferase system. J Biol Chem. 1979 Jan 25;254(2):249–252. [PubMed] [Google Scholar]
  10. Jacobson G. R., Saraceni-Richards C. The Escherichia coli mannitol permease as a model for transport via the bacterial phosphotransferase system. J Bioenerg Biomembr. 1993 Dec;25(6):621–626. doi: 10.1007/BF00770249. [DOI] [PubMed] [Google Scholar]
  11. Khandekar S. S., Jacobson G. R. Evidence for two distinct conformations of the Escherichia coli mannitol permease that are important for its transport and phosphorylation functions. J Cell Biochem. 1989 Feb;39(2):207–216. doi: 10.1002/jcb.240390212. [DOI] [PubMed] [Google Scholar]
  12. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  13. Lee C. A., Saier M. H., Jr Mannitol-specific enzyme II of the bacterial phosphotransferase system. III. The nucleotide sequence of the permease gene. J Biol Chem. 1983 Sep 10;258(17):10761–10767. [PubMed] [Google Scholar]
  14. Lengeler J. W., Titgemeyer F., Vogler A. P., Wöhrl B. M. Structures and homologies of carbohydrate: phosphotransferase system (PTS) proteins. Philos Trans R Soc Lond B Biol Sci. 1990 Jan 30;326(1236):489–504. doi: 10.1098/rstb.1990.0027. [DOI] [PubMed] [Google Scholar]
  15. Lengeler J. W., Vogler A. P. Molecular mechanisms of bacterial chemotaxis towards PTS-carbohydrates. FEMS Microbiol Rev. 1989 Jun;5(1-2):81–92. doi: 10.1016/0168-6445(89)90011-9. [DOI] [PubMed] [Google Scholar]
  16. Lolkema J. S., Dijkstra D. S., Robillard G. T. Mechanics of solute translocation catalyzed by enzyme IImtl of the phosphoenolpyruvate-dependent phosphotransferase system of Escherichia coli. Biochemistry. 1992 Jun 23;31(24):5514–5521. doi: 10.1021/bi00139a013. [DOI] [PubMed] [Google Scholar]
  17. Lolkema J. S., Dijkstra D. S., ten Hoeve-Duurkens R. H., Robillard G. T. Interaction between the cytoplasmic and membrane-bound domains of enzyme IImtl of the Escherichia coli phosphoenolpyruvate-dependent phosphotransferase system. Biochemistry. 1991 Jul 9;30(27):6721–6726. doi: 10.1021/bi00241a013. [DOI] [PubMed] [Google Scholar]
  18. Lolkema J. S., Dijkstra D. S., ten Hoeve-Duurkens R. H., Robillard G. T. The membrane-bound domain of the phosphotransferase enzyme IImtl of Escherichia coli constitutes a mannitol translocating unit. Biochemistry. 1990 Nov 27;29(47):10659–10663. doi: 10.1021/bi00499a012. [DOI] [PubMed] [Google Scholar]
  19. Lolkema J. S., ten Hoeve-Duurkens R. H., Dijkstra D. S., Robillard G. T. Mechanistic coupling of transport and phosphorylation activity by enzyme IImtl of the Escherichia coli phosphoenolpyruvate-dependent phosphotransferase system. Biochemistry. 1991 Jul 9;30(27):6716–6721. doi: 10.1021/bi00241a012. [DOI] [PubMed] [Google Scholar]
  20. Manayan R., Tenn G., Yee H. B., Desai J. D., Yamada M., Saier M. H., Jr Genetic analyses of the mannitol permease of Escherichia coli: isolation and characterization of a transport-deficient mutant which retains phosphorylation activity. J Bacteriol. 1988 Mar;170(3):1290–1296. doi: 10.1128/jb.170.3.1290-1296.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Mandel M., Higa A. Calcium-dependent bacteriophage DNA infection. J Mol Biol. 1970 Oct 14;53(1):159–162. doi: 10.1016/0022-2836(70)90051-3. [DOI] [PubMed] [Google Scholar]
  22. Meadow N. D., Fox D. K., Roseman S. The bacterial phosphoenolpyruvate: glycose phosphotransferase system. Annu Rev Biochem. 1990;59:497–542. doi: 10.1146/annurev.bi.59.070190.002433. [DOI] [PubMed] [Google Scholar]
  23. Pas H. H., Meyer G. H., Kruizinga W. H., Tamminga K. S., van Weeghel R. P., Robillard G. T. 31phospho-NMR demonstration of phosphocysteine as a catalytic intermediate on the Escherichia coli phosphotransferase system EIIMtl. J Biol Chem. 1991 Apr 15;266(11):6690–6692. [PubMed] [Google Scholar]
  24. Pas H. H., Robillard G. T. S-phosphocysteine and phosphohistidine are intermediates in the phosphoenolpyruvate-dependent mannitol transport catalyzed by Escherichia coli EIIMtl. Biochemistry. 1988 Aug 9;27(16):5835–5839. doi: 10.1021/bi00416a002. [DOI] [PubMed] [Google Scholar]
  25. Pas H. H., ten Hoeve-Duurkens R. H., Robillard G. T. Bacterial phosphoenolpyruvate-dependent phosphotransferase system: mannitol-specific EII contains two phosphoryl binding sites per monomer and one high-affinity mannitol binding site per dimer. Biochemistry. 1988 Jul 26;27(15):5520–5525. doi: 10.1021/bi00415a020. [DOI] [PubMed] [Google Scholar]
  26. Postma P. W., Lengeler J. W., Jacobson G. R. Phosphoenolpyruvate:carbohydrate phosphotransferase systems of bacteria. Microbiol Rev. 1993 Sep;57(3):543–594. doi: 10.1128/mr.57.3.543-594.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Ruijter G. J., van Meurs G., Verwey M. A., Postma P. W., van Dam K. Analysis of mutations that uncouple transport from phosphorylation in enzyme IIGlc of the Escherichia coli phosphoenolpyruvate-dependent phosphotransferase system. J Bacteriol. 1992 May;174(9):2843–2850. doi: 10.1128/jb.174.9.2843-2850.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Saier M. H., Jr, Reizer J. Proposed uniform nomenclature for the proteins and protein domains of the bacterial phosphoenolpyruvate: sugar phosphotransferase system. J Bacteriol. 1992 Mar;174(5):1433–1438. doi: 10.1128/jb.174.5.1433-1438.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Simoni R. D., Roseman S., Saier M. H., Jr Sugar transport. Properties of mutant bacteria defective in proteins of the phosphoenolpyruvate: sugar phosphotransferase system. J Biol Chem. 1976 Nov 10;251(21):6584–6597. [PubMed] [Google Scholar]
  30. Stephan M. M., Jacobson G. R. Membrane disposition of the Escherichia coli mannitol permease: identification of membrane-bound and cytoplasmic domains. Biochemistry. 1986 Dec 16;25(25):8230–8234. doi: 10.1021/bi00373a016. [DOI] [PubMed] [Google Scholar]
  31. Stephan M. M., Jacobson G. R. Subunit interactions of the Escherichia coli mannitol permease: correlation with enzymic activities. Biochemistry. 1986 Jul 15;25(14):4046–4051. doi: 10.1021/bi00362a009. [DOI] [PubMed] [Google Scholar]
  32. Sugiyama J. E., Mahmoodian S., Jacobson G. R. Membrane topology analysis of Escherichia coli mannitol permease by using a nested-deletion method to create mtlA-phoA fusions. Proc Natl Acad Sci U S A. 1991 Nov 1;88(21):9603–9607. doi: 10.1073/pnas.88.21.9603. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Weng Q. P., Elder J., Jacobson G. R. Site-specific mutagenesis of residues in the Escherichia coli mannitol permease that have been suggested to be important for its phosphorylation and chemoreception functions. J Biol Chem. 1992 Sep 25;267(27):19529–19535. [PubMed] [Google Scholar]
  34. Weng Q. P., Jacobson G. R. Role of a conserved histidine residue, His-195, in the activities of the Escherichia coli mannitol permease. Biochemistry. 1993 Oct 19;32(41):11211–11216. doi: 10.1021/bi00092a034. [DOI] [PubMed] [Google Scholar]
  35. White D. W., Jacobson G. R. Molecular cloning of the C-terminal domain of Escherichia coli D-mannitol permease: expression, phosphorylation, and complementation with C-terminal permease deletion proteins. J Bacteriol. 1990 Mar;172(3):1509–1515. doi: 10.1128/jb.172.3.1509-1515.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. van Weeghel R. P., Meyer G. H., Keck W., Robillard G. T. Phosphoenolpyruvate-dependent mannitol phosphotransferase system of Escherichia coli: overexpression, purification, and characterization of the enzymatically active C-terminal domain of enzyme IImtl equivalent to enzyme IIImtl. Biochemistry. 1991 Feb 19;30(7):1774–1779. doi: 10.1021/bi00221a007. [DOI] [PubMed] [Google Scholar]
  37. van Weeghel R. P., Meyer G., Pas H. H., Keck W., Robillard G. T. Cytoplasmic phosphorylating domain of the mannitol-specific transport protein of the phosphoenolpyruvate-dependent phosphotransferase system in Escherichia coli: overexpression, purification, and functional complementation with the mannitol binding domain. Biochemistry. 1991 Oct 1;30(39):9478–9485. doi: 10.1021/bi00103a013. [DOI] [PubMed] [Google Scholar]
  38. van Weeghel R. P., van der Hoek Y. Y., Pas H. H., Elferink M., Keck W., Robillard G. T. Details of mannitol transport in Escherichia coli elucidated by site-specific mutagenesis and complementation of phosphorylation site mutants of the phosphoenolpyruvate-dependent mannitol-specific phosphotransferase system. Biochemistry. 1991 Feb 19;30(7):1768–1773. doi: 10.1021/bi00221a006. [DOI] [PubMed] [Google Scholar]

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