SUBUNIT-E OF THE VACUOLAR H-ATPASE OF HORDEUM-VULGARE L - CDNA CLONING, EXPRESSION AND IMMUNOLOGICAL ANALYSIS()

A tonoplast protein of 31 kDa apparent molecular mass (TpP 31) was iso lated from two-dimensional gels. Amino acid sequences were determined from LysC endoproteinase-peptide fragments. Using degenerate oligonucl eotides, a corresponding cDNA clone of 1034 bp was isolated from a bar ley leaf cDNA library. It encodes for subunit E of the vacuolar H+-ATP ase, the first one identi fled in plants so far. The open reading fram e extends over 681 bp, encoding a gene product of 227 amino acids and a calculated molecular weight of 26 228 g mol(-1). Northern and Wester n blot analysis indicates constitutive expression of subunit E in all plant organs with only small effects of salt stress. Localization of T pP 31 at the tonoplast was confirmed in fractions of purified vacuolar membrane obtained by free-flow electrophoresis. Immunoprecipitation o f newly synthesized S-35-labelled membrane proteins with anti-TpP 31 g ave two additional bands with apparent molecular masses of about 53 an d 62 kDa. Gel filtration after mild solubilization showed co-purificat ion of TpP 31 with the 55 kDa subunit of the H+-ATPase. Both results p rovide evidence beyond the sequence homology that TpP 31 is a structur al component of the vacuolar H+-ATPase.