Salinity tolerance in halophytes

被引:1872
作者
Flowers, Timothy J. [1 ,2 ]
Colmer, Timothy D. [2 ]
机构
[1] Univ Sussex, Sch Life Sci, Brighton BN1 9QG, E Sussex, England
[2] Univ Western Australia, Fac Nat & Agr Sci, Sch Plant Biol, Crawley, WA 6009, Australia
关键词
chloride; compatible solutes; halophyte; ion transport; osmotic adjustment; potassium; salt and stress tolerance; sodium;
D O I
10.1111/j.1469-8137.2008.02531.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Halophytes, plants that survive to reproduce in environments where the salt concentration is around 200 mM NaCl or more, constitute about 1% of the world's flora. Some halophytes show optimal growth in saline conditions; others grow optimally in the absence of salt. However, the tolerance of all halophytes to salinity relies on controlled uptake and compartmentalization of Na+, K+ and Cl- and the synthesis of organic 'compatible' solutes, even where salt glands are operative. Although there is evidence that different species may utilize different transporters in their accumulation of Na+, in general little is known of the proteins and regulatory networks involved. Consequently, it is not yet possible to assign molecular mechanisms to apparent differences in rates of Na+ and Cl- uptake, in root-to-shoot transport (xylem loading and retrieval), or in net selectivity for K+ over Na+. At the cellular level, H+-ATPases in the plasma membrane and tonoplast, as well as the tonoplast H+-PP(i)ase, provide the trans-membrane proton motive force used by various secondary transporters. The widespread occurrence, taxonomically, of halophytes and the general paucity of information on the molecular regulation of tolerance mechanisms persuade us that research should be concentrated on a number of 'model' species that are representative of the various mechanisms that might be involved in tolerance.
引用
收藏
页码:945 / 963
页数:19
相关论文
共 201 条
[1]   Growth and development of Mesembryanthemum crystallinum (Aizoaceae) [J].
Adams, P ;
Nelson, DE ;
Yamada, S ;
Chmara, W ;
Jensen, RG ;
Bohnert, HJ ;
Griffiths, H .
NEW PHYTOLOGIST, 1998, 138 (02) :171-190
[2]   DIFFERENT PHYSIOTYPES AMONG HALOPHYTES FROM REGION EAST OF LAKE NEUSIEDLERSEE (AUSTRIA) [J].
ALBERT, R ;
KINZEL, H .
ZEITSCHRIFT FUR PFLANZENPHYSIOLOGIE, 1973, 70 (02) :138-157
[3]  
Albert R, 2000, ERGEBNISSE WELTWEITE, P69
[4]   Abiotic stress and plant genome evolution. Search for new models [J].
Amtmann, A ;
Bohnert, HJ ;
Bressan, RA .
PLANT PHYSIOLOGY, 2005, 138 (01) :127-130
[5]  
[Anonymous], PLANT CELL ENV
[6]   Na+ transport in plants [J].
Apse, Maris P. ;
Blumwald, Eduardo .
FEBS LETTERS, 2007, 581 (12) :2247-2254
[7]   Contrasting patterns of leaf solute accumulation and salt adaptation in four phreatophytic desert plants in a hyperarid desert with saline groundwater [J].
Arndt, SK ;
Arampatsis, C ;
Foetzki, A ;
Li, XY ;
Zeng, FJ ;
Zhang, XM .
JOURNAL OF ARID ENVIRONMENTS, 2004, 59 (02) :259-270
[8]  
Aronson JA, 1989, HALOPH DATA BASE SAL
[9]   STUDIES IN HALOPHYTES .3. SALINITY FACTORS IN THE GROWTH OF AUSTRALIAN SALTBUSHES [J].
ASHBY, WC ;
BEADLE, NCW .
ECOLOGY, 1957, 38 (02) :344-352
[10]   Effects of salinity levels on proteome of Suaeda aegyptiaca leaves [J].
Askari, H ;
Edqvist, J ;
Hajheidari, M ;
Kafi, M ;
Salekdeh, GH .
PROTEOMICS, 2006, 6 (08) :2542-2554