Cloning of the PpNHAD1 transporter of Physcomitrella patens, a chloroplast transporter highly conserved in photosynthetic eukaryotic organisms

被引:15
作者
Barrero-Gil, Javier [1 ]
Rodriguez-Navarro, Alonso [1 ]
Benito, Begona [1 ]
机构
[1] Univ Politecn Madrid, Dept Biotecnol, E-28040 Madrid, Spain
关键词
antiporter; chloroplast; lithium; NHAD; Physcomitrella; potassium; sodium;
D O I
10.1093/jxb/erm094
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
A cDNA that encodes a transporter from the NHAD family was identified in Physcomitrella patens. Computer-based searches using the amino acid sequence of PpNHAD1 revealed that, in addition to being expressed in flowering plants, highly conserved transporters of this family are expressed in red algae, green algae, mosses, liverworts, and photosynthetic stramenopiles, but not in heterotrophic stramenopiles. A chloroplast transit peptide was detected in PpNHAD1 and in most of the related sequences, indicating that PpNHAD1 is a chloroplast transporter. A PpNHAD1-GFP fusion localized to the chloroplast in Physcomitrella protoplasts, and truncation of the N-terminus of the protein dispersed the fluorescence signal outside the chloroplast. PpNHAD1 did not show functional expression in either yeast or bacterial mutants, but truncated proteins with shorter N-termini, PpNHAD1-1 and PpNHAD1-2, could be functionally expressed in bacteria. PpNHAD1-1 alleviated the Li+ intolerance of a Na+-efflux Escherichia coli mutant at acidic pH values. Both PpNHAD1-1 and PpNHAD1-2 reduced the K+ requirements of a K+-infflux E. coli mutant more actively at high pH values. PpNHAD1 seems to be an important transporter that mediates ionic homeostasis in chloroplasts from red algae to flowering plants.
引用
收藏
页码:2839 / 2849
页数:11
相关论文
共 52 条
[1]
Two p-type ATPases are required for copper delivery in Arabidopsis thaliana chloroplasts [J].
Abdel-Ghany, SE ;
Müller-Moulé, P ;
Niyogi, KK ;
Pilon, M ;
Shikanai, T .
PLANT CELL, 2005, 17 (04) :1233-1251
[2]
ISOLATION AND PHYSIOLOGICAL ANALYSIS OF MUTANTS OF THE MOSS, PHYSCOMITRELLA-PATENS, WHICH OVER-PRODUCE GAMETOPHORES [J].
ASHTON, NW ;
COVE, DJ ;
FEATHERSTONE, DR .
PLANTA, 1979, 144 (05) :437-442
[3]
INTERCONVERSION OF COMPONENTS OF THE BACTERIAL PROTON MOTIVE FORCE BY ELECTROGENIC POTASSIUM-TRANSPORT [J].
BAKKER, EP ;
MANGERICH, WE .
JOURNAL OF BACTERIOLOGY, 1981, 147 (03) :820-826
[4]
Bañuelos MA, 1998, MICROBIOL-UK, V144, P2749, DOI 10.1099/00221287-144-10-2749
[5]
Molecular cloning and characterization of a sodium-pump ATPase of the moss Physcomitrella patens [J].
Benito, B ;
Rodríguez-Navarro, A .
PLANT JOURNAL, 2003, 36 (03) :382-389
[6]
A SERIES OF YEAST/ESCHERICHIA COLI LAMBDA EXPRESSION VECTORS DESIGNED FOR DIRECTIONAL CLONING OF CDNAS AND CRE/LOX-MEDIATED PLASMID EXCISION [J].
BRUNELLI, JP ;
PALL, ML .
YEAST, 1993, 9 (12) :1309-1318
[7]
The sodium cycle in Vibrio cholerae:: Riddles in the dark [J].
Dibrov, P .
BIOCHEMISTRY-MOSCOW, 2005, 70 (02) :150-153
[8]
Cloning, functional expression in Escherichia coli and primary characterization of a new Na+/H+ antiporter, NhaD, of Vibrio cholerae [J].
Dzioba, J ;
Ostroumov, E ;
Winogrodzki, A ;
Dibrov, P .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2002, 229 (1-2) :119-124
[9]
Predicting subcellular localization of proteins based on their N-terminal amino acid sequence [J].
Emanuelsson, O ;
Nielsen, H ;
Brunak, S ;
von Heijne, G .
JOURNAL OF MOLECULAR BIOLOGY, 2000, 300 (04) :1005-1016
[10]
ChloroP, a neural network-based method for predicting chloroplast transit peptides and their cleavage sites [J].
Emanuelsson, O ;
Nielsen, H ;
Von Heijne, G .
PROTEIN SCIENCE, 1999, 8 (05) :978-984