Hydraulic conductance and mercury-sensitive water transport for roots of Opuntia acanthocarpa in relation to soil drying and rewetting

被引:76
作者
Martre, P
North, GB
Nobel, PS [1 ]
机构
[1] Univ Calif Los Angeles, Dept Organism Biol Ecol & Evolut, Los Angeles, CA 90095 USA
[2] Occidental Coll, Dept Biol, Los Angeles, CA 90041 USA
关键词
D O I
10.1104/pp.126.1.352
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Drought-induced changes in root hydraulic conductance (L-P) and mercury-sensitive water transport were examined for distal (immature) and mid-root (mature) regions of Opuntia acanthocarpa. During 45 d of soil drying, L-P decreased by about 67% for distal and mid-root regions. After 8 d in rewetted soil, L-P recovered to 60% of its initial value for both regions. Axial xylem hydraulic conductivity was only a minor limiter of L-P. Under wet conditions, HECl2 (50 muM), which is known to block membrane water-transport channels (aquaporins), decreased L-P and the radial hydraulic conductance for the stele (L-R,L- S) of the distal root region by 32% and 41%, respectively; both L-P and L-R,L- S recovered fully after transfer to 2-mercaptoethanol (10 mM). In contrast, HgCl2 did not inhibit L-P of the mid-root region under wet conditions, although it reduced L-R,L- S by 41%. Under dry conditions, neither L-P nor L-R,L- S of the two root regions was inhibited by HgCl2. After 8 d of rewetting, HgCl2, decreased L-P and L-R,L- S of the distal region by 23% and 32%, respectively, but L-P and L-R,L- S of the mid-root region were unaltered. Changes in putative aquaporin activity accounted for about 38% of the reduction in L-R,L- S in drying soil and for 61% of its recovery for the distal region 8 d after rewetting. In the stele, changes in aquaporin activity accounted for about 74% of the variable L-R,L- S during drought and after rewetting. Thus, aquaporins are important for regulating water movement for roots of O. acanthocarpa.
引用
收藏
页码:352 / 362
页数:11
相关论文
共 51 条
[1]   High expression of the tonoplast aquaporin ZmTIP1 in epidermal and conducting tissues of maize [J].
Barrieu, F ;
Chaumont, F ;
Chrispeels, MJ .
PLANT PHYSIOLOGY, 1998, 117 (04) :1153-1163
[2]   Radial hydraulic conductivity along developing onion roots [J].
Barrowclough, DE ;
Peterson, CA ;
Steudle, E .
JOURNAL OF EXPERIMENTAL BOTANY, 2000, 51 (344) :547-557
[3]   Does calcium ameliorate the negative effect of NaCl on melon root water transport by regulating aquaporin activity? [J].
Carvajal, M ;
Cerdá, A ;
Martínez, V .
NEW PHYTOLOGIST, 2000, 145 (03) :439-447
[4]   Physiological function of water channels as affected by salinity in roots of paprika pepper [J].
Carvajal, M ;
Martínez, V ;
Alcaraz, CF .
PHYSIOLOGIA PLANTARUM, 1999, 105 (01) :95-101
[5]  
Carvajal M, 1996, PLANTA, V199, P372, DOI 10.1007/BF00195729
[6]   Characterization of a maize tonoplast aquaporin expressed in zones of cell division and elongation [J].
Chaumont, F ;
Barrieu, F ;
Herman, EM ;
Chrispeels, MJ .
PLANT PHYSIOLOGY, 1998, 117 (04) :1143-1152
[7]   STRUCTURAL-CHANGES AND ASSOCIATED REDUCTION OF HYDRAULIC CONDUCTANCE IN ROOTS OF SORGHUM-BICOLOR L FOLLOWING EXPOSURE TO WATER DEFICIT [J].
CRUZ, RT ;
JORDAN, WR ;
DREW, MC .
PLANT PHYSIOLOGY, 1992, 99 (01) :203-212
[8]   THE PLASMA-MEMBRANE OF ARABIDOPSIS-THALIANA CONTAINS A MERCURY-INSENSITIVE AQUAPORIN THAT IS A HOMOLOG OF THE TONOPLAST WATER CHANNEL PROTEIN TIP [J].
DANIELS, MJ ;
MIRKOV, TE ;
CHRISPEELS, MJ .
PLANT PHYSIOLOGY, 1994, 106 (04) :1325-1333
[9]   Modelling of the hydraulic architecture of root systems: An integrated approach to water absorption - Model description [J].
Doussan, C ;
Pages, L ;
Vercambre, G .
ANNALS OF BOTANY, 1998, 81 (02) :213-223
[10]   Effects of exposure to humid air on epidermal viability and suberin deposition in maize (Zea mays L.) roots [J].
Enstone, DE ;
Peterson, CA .
PLANT CELL AND ENVIRONMENT, 1998, 21 (08) :837-844