Missense mutations that inactivate the Aspergillus nidulans nrtA gene encoding a high-affinity nitrate transporter

James Robertson Kinghorn, J Sloan, GJM Kana'n, ER DaSilva, DA Rouch, Sheila Eileen Unkles

Research output: Contribution to journalArticlepeer-review

Abstract

The transport of nitrate into prokaryotic and eukaryotic cells, of considerable interest to agriculture, ecology, and human health, is carried out by members of a distinct cluster of proteins within the major facilitator superfamily. To obtain structure/function information on this important class of nitrate permeases, a collection of chemically induced mutations in the nrtA gene encoding a 12-transmembrane domain, high-affinity nitrate transporter from the eukaryote Aspergillus nidulans was isolated and characterized. This mutational analysis, coupled with protein alignments, demonstrates the utility of the approach to predicting peptide motifs and individual residues important for the movement of nitrate across the membrane. These include the highly conserved nitrate signature motif (residues 166-173) in Tm 5, the conserved charged residues Arg87 (Tm 2) and Arg368 (Tm 8), as well as the aromatic residue Phc47 (Tm 1), all within transmembrane helices. No mutations were observed in the large central loop (Lp 6/7) between Tm 6 and Tm 7. Finally, the study of a strain with a conversion of Trp481 (Tm 12) to a stop codon suggests that all 12 transmembrane domains and/or the C-terminal tail are required for membrane insertion and/or stability of NrtA.

Original languageEnglish
Pages (from-to)1369-1377
Number of pages9
JournalGenetics
Volume169
Issue number3
DOIs
Publication statusPublished - Mar 2005

Keywords

  • MAJOR FACILITATOR SUPERFAMILY
  • BACTERIAL OXALATE TRANSPORTER
  • ESCHERICHIA-COLI
  • LACTOSE PERMEASE
  • CHLORATE TOXICITY
  • MEMBRANE-PROTEINS
  • CONSERVED MOTIF
  • ASSIMILATION
  • MECHANISM
  • BIOSYNTHESIS

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