Literature DB >> 7907327

Functional roles of Glu-269 and Glu-325 within the lactose permease of Escherichia coli.

P J Franco1, R J Brooker.   

Abstract

Acidic residues which are found on transmembrane segments within the lactose permease may play an important role in H+ and/or sugar recognition. To examine the functional roles of Glu-269 and Glu-325, we have constructed a variety of amino acid substitutions (e.g. aspartate, glycine, alanine, serine, or glutamine) via site-directed mutagenesis. At position 269, all mutations appear to have a detrimental effect on sugar affinity, downhill transport, and counterflow. The Asp-269 mutant was able to accumulate lactose against a concentration gradient, whereas all of the nonionizable substitutions at position 269 were completely defective. Nevertheless, in spite of their inability to actively accumulate sugars, Gly-269, Ala-269, and Gln-269 mutants were observed to transport H+ upon the addition of galactosides. Mutations at position 325 had a markedly different phenotype. For example, the Asp-325, Gly-325, and Gln-325 mutants exhibited an apparent Km for lactose transport (e.g. 0.21, 0.47, and 0.50 mM, respectively), which was actually lower than that of the wild-type strain (1.44 mM). In counterflow assays, all position 325 mutants also appear to catalyze lactose exchange. Similar to the results obtained at position 269, the Asp-325 mutant exhibited moderate levels of accumulation, whereas none of the nonionizable mutations at position 325 were able to accumulate galactosides against a concentration gradient. However, unlike the position 269 mutants, no H+ transport was observed in the Gly-325, Ala-325, Ser-325, or Gln-325 strains upon the addition of lactose, S-beta-D-galactopyranosyl-(1,1)-beta-thiogalactopyranoside, 1-O-methyl-beta-D-galactopyranoside, or melibiose. Furthermore, in these mutants, the efflux of lactose during counterflow assays became insensitive to delta pH. Overall, these results are consistent with the notion that an acidic residue at position 325 is required for H+ transport via the lactose permease. Alternative hypotheses are also discussed.

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Year:  1994        PMID: 7907327

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  28 in total

1.  Arg-52 in the melibiose carrier of Escherichia coli is important for cation-coupled sugar transport and participates in an intrahelical salt bridge.

Authors:  P J Franco; T H Wilson
Journal:  J Bacteriol       Date:  1999-10       Impact factor: 3.490

Review 2.  A functional-phylogenetic classification system for transmembrane solute transporters.

Authors:  M H Saier
Journal:  Microbiol Mol Biol Rev       Date:  2000-06       Impact factor: 11.056

3.  Unraveling the mechanism of the lactose permease of Escherichia coli.

Authors:  M Sahin-Tóth; A Karlin; H R Kaback
Journal:  Proc Natl Acad Sci U S A       Date:  2000-09-26       Impact factor: 11.205

4.  Control of H+/lactose coupling by ionic interactions in the lactose permease of Escherichia coli.

Authors:  J L Johnson; R J Brooker
Journal:  J Membr Biol       Date:  2004-04-01       Impact factor: 1.843

5.  Binding affinity of lactose permease is not altered by the H+ electrochemical gradient.

Authors:  Lan Guan; H Ronald Kaback
Journal:  Proc Natl Acad Sci U S A       Date:  2004-08-10       Impact factor: 11.205

6.  Structure of a fucose transporter in an outward-open conformation.

Authors:  Shangyu Dang; Linfeng Sun; Yongjian Huang; Feiran Lu; Yufeng Liu; Haipeng Gong; Jiawei Wang; Nieng Yan
Journal:  Nature       Date:  2010-09-26       Impact factor: 49.962

Review 7.  Energy coupling mechanisms of MFS transporters.

Authors:  Xuejun C Zhang; Yan Zhao; Jie Heng; Daohua Jiang
Journal:  Protein Sci       Date:  2015-09-18       Impact factor: 6.725

Review 8.  Lessons from lactose permease.

Authors:  Lan Guan; H Ronald Kaback
Journal:  Annu Rev Biophys Biomol Struct       Date:  2006

9.  The role of helix VIII in the lactose permease of Escherichia coli: II. Site-directed sulfhydryl modification.

Authors:  S Frillingos; H R Kaback
Journal:  Protein Sci       Date:  1997-02       Impact factor: 6.725

10.  The role of helix VIII in the lactose permease of Escherichia coli: I. Cys-scanning mutagenesis.

Authors:  S Frillingos; M L Ujwal; J Sun; H R Kaback
Journal:  Protein Sci       Date:  1997-02       Impact factor: 6.725

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