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Plant Physiol, May 2000, Vol. 123, pp. 353-362
AVP2, a Sequence-Divergent, K+-Insensitive
H+-Translocating Inorganic Pyrophosphatase from
Arabidopsis1
Yolanda M.
Drozdowicz,
Jessica C.
Kissinger, and
Philip A.
Rea*
Plant Science Institute, Department of Biology, University of
Pennsylvania, Philadelphia, Pennsylvania 19104-6018
Plant vacuolar H+-translocating inorganic
pyrophosphatases (V-PPases; EC 3.6.1.1) have been considered to
constitute a family of functionally and structurally monotonous
intrinsic membrane proteins. Typified by AVP1 (V. Sarafian, Y. Kim,
R.J. Poole, P.A. Rea [1992] Proc Natl Acad Sci USA 89: 1775-1779)
from Arabidopsis, all characterized plant V-PPases share greater than
84% sequence identity and catalyze K+-stimulated
H+ translocation. Here we describe the molecular and
biochemical characterization of AVP2 (accession no. AF182813), a
sequence-divergent (36% identical) K+-insensitive,
Ca2+-hypersensitive V-PPase active in both inorganic
pyrophosphate hydrolysis and H+ translocation. The
differences between AVP2 and AVP1 provide the first indication that
plant V-PPases from the same organism fall into two distinct
categories. Phylogenetic analyses of these and other V-PPase sequences
extend this principle by showing that AVP2, rather than being an
isoform of AVP1, is but one representative of a novel category of
AVP2-like (type II) V-PPases that coexist with AVP1-like (type I)
V-PPases not only in plants, but also in apicomplexan protists such as
the malarial parasite Plasmodium falciparum.
1
This work was supported by the Department of
Energy (grant no. DE-FG02-91ER20055 to P.A.R.). Y.M.D. is a Triagency
(Department of Energy/National Science Foundation/U.S. Department of
Agriculture) Plant Training Grant Fellow. Sequencing
of the Chlorobium tepidum and Caulobacter
crescentus genomes by The Institute for Genomic Research was
accomplished with support from the Department of Energy. Partial
sequencing of the P. falciparum genome was accomplished by The Institute for Genomic Research, The Sanger Centre, and the
Stanford DNA Sequencing and Technology Center as part of the Malaria
Genome Project with support from the National Institute of Allergy and
Infectious Diseases, National Institutes of Health, The Wellcome Trust,
and The Burroughs Wellcome Fund.
*
Corresponding author; e-mail parea{at}sas.upenn.edu; fax 215-
898-8780.
© 2000 American Society of Plant Physiologists
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