Journal of Experimental Botany, Vol 50, 139-140, Copyright © 1999 by Oxford University Press
M Ikeda, M Rahman, C Moritani, K Umami, Y Tanimura, R Akagi, Y Tanaka, M Maeshima and Y Watanabe
An almost complete cDNA clone [pPPI (AcVP gene), 3104
bp in length/open reading frame from 795 to 2960 bp/721 amino acids with a
molecular weight of 74 406] encoding Acetabularia
H+-translocating inorganic pyrophosphatase was
isolated from total RNA using reverse-transcription and PCR techniques.
Alignments of the primary structure to that of similar enzymes in higher
plants and Rhodospirillum rubrum revealed that overall
similarities were around 50%, the C-terminal half was well conserved but
the N-terminal half showed divergencies except in a postulated
substrate-binding domain. By Northern analysis, about 3.2 kb RNA mainly
hybridized with 5
ARTICLES
Gene note. A vacuolar H+-pyrophosphatase in Acetabularia acetabulum: molecular cloning and comparison with higher plants and a bacterium
Faculty of Health and Welfare Science, Okayam Prefectural University, Kuboki 111, Soja 719-11, Japan; Faculty of Pharmaceutical Sciences, Okayama University, Tsushima-Naka-1, Okayama 700, Japan; Chemical Tolerance, National Institute of Agrobiological Resources, Tsukuba Ibaraki 305, Japan; Faculty of Agricultural Sciences, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-01, Japan; Corresponding author; Fax: +81 866 94 2152; E-mail: mikieda@fhw.oka-pu.ac.jp
-untranslated region specific RNA probe of the
AcVP gene.Keywords: inorganic
pyrophosphatase, vacuole, H+-translocation,
molecular cloning, Acetabularia acetabulum
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