Characterization of the double mutant, Val-177/Asn-322, of the lactose permease

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Abstract

The double mutant, Val-177/Asn-322, was investigated with regard to its ability to transport H+ and galactosides. In downhill lactose transport assays, the wild-type strain had a Km value for lactose uptake of 0.9 mM and a Vmax of 0.65 μmol lactose/min·mg protein while the mutant had a significantly higher Km, value of 1.9 mM but a similar Vmax of 0.49 μmol/min·mg protein. In spite of its moderate ability to transport lactose downhill, the Val-177/Asn-322 mutant exhibited the striking property of being completely defective in the uphill accumulation of lactose or methyl-β-D-thiogalactopyranoside. Direct measurements of H+ transport, however, showed that the mutant's defect in active accumulation is not due to a defect in the ability to transport H+ with lactose or methyl-β-D-thiogalactopyranoside. The Val-177/Asn-322 mutant strain had a H+:lactose stoichiometry of 0.84 which was similar to that measured in the wild-type strain (0.68). These results are discussed with regard to the role His-322 plays in H+ transport, active accumulation of sugars, and sugar recognition.

Original languageEnglish (US)
Pages (from-to)4155-4160
Number of pages6
JournalJournal of Biological Chemistry
Volume265
Issue number7
StatePublished - Mar 5 1990

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Lactose
Thiogalactosides
Sugars
Galactosides
Defects
Active Biological Transport
Mutant Proteins
lactose permease
Stoichiometry
Assays
Proteins

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Characterization of the double mutant, Val-177/Asn-322, of the lactose permease. / Brooker, Robert J.

In: Journal of Biological Chemistry, Vol. 265, No. 7, 05.03.1990, p. 4155-4160.

Research output: Contribution to journalArticle

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