Peroxidases have more functions than a Swiss army knife

被引:836
作者
Passardi, F [1 ]
Cosio, C [1 ]
Penel, C [1 ]
Dunand, C [1 ]
机构
[1] Univ Geneva, Lab Plant Physiol, CH-1211 Geneva, Switzerland
关键词
evolution; ROS (abiotic and biotic) stress; cell wall loosening and cross-linking; senescence; fruit ripening; symbiosis;
D O I
10.1007/s00299-005-0972-6
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Plant peroxidases (class III peroxidases) are present in all land plants. They are members of a large multigenic family. Probably due to this high number of isoforms, and to a very heterogeneous regulation of their expression, plant peroxidases are involved in a broad range of physiological processes all along the plant life cycle. Due to two possible catalytic cycles, peroxidative and hydroxylic, peroxidases can generate reactive oxygen species (ROS) ((OH)-O-center dot, HOO center dot), polymerise cell wall compounds, and regulate H2O2 levels. By modulating their activity and expression following internal and external stimuli, peroxidases are prevalent at every stage of plant growth, including the demands that the plant meets in stressful conditions. These multifunctional enzymes can build a rigid wall or produce ROS to make it more flexible; they can prevent biological and chemical attacks by raising physical barriers or by counterattacking with a large production of ROS; they can be involved in a more peaceful symbiosis. They are finally present from the first hours of a plant's life until its last moments. Although some functions look paradoxical, the whole process is probably regulated by a fine-tuning that has yet to be elucidated. This review will discuss the factors that can influence this delicate balance.
引用
收藏
页码:255 / 265
页数:11
相关论文
共 107 条
[1]   Differential leaf stress responses in young and senescent plants [J].
Abarca, D ;
Martin, M ;
Sabater, B .
PHYSIOLOGIA PLANTARUM, 2001, 113 (03) :409-415
[2]   Phytoremediation of 2,4-dichlorophenol by Brassica napus hairy root cultures [J].
Agostini, E ;
Coniglio, MS ;
Milrad, SR ;
Tigier, HA ;
Giulietti, AM .
BIOTECHNOLOGY AND APPLIED BIOCHEMISTRY, 2003, 37 (02) :139-144
[3]   CHITINASE AND PEROXIDASE-ACTIVITIES ARE INDUCED IN EUCALYPTUS ROOTS ACCORDING TO AGGRESSIVENESS OF AUSTRALIAN ECTOMYCORRHIZAL STRAINS OF PISOLITHUS SP [J].
ALBRECHT, C ;
BURGESS, T ;
DELL, B ;
LAPEYRIE, F .
NEW PHYTOLOGIST, 1994, 127 (02) :217-222
[4]   Ethylene biosynthesis and action in tomato: a model for climacteric fruit ripening [J].
Alexander, L ;
Grierson, D .
JOURNAL OF EXPERIMENTAL BOTANY, 2002, 53 (377) :2039-2055
[5]   PSEUDONODULATION OF LEGUMINOUS PLANTS INDUCED BY 2-BROMO-3,5-DICHLOROBENZOIC ACID [J].
ALLEN, EK ;
ALLEN, ON ;
NEWMAN, AS .
AMERICAN JOURNAL OF BOTANY, 1953, 40 (06) :429-435
[6]   Differential activity of peroxidase isozymes in response to wounding, gypsy moth, and plant hormones in northern red oak (Quercus rubra L.) [J].
Allison, SD ;
Schultz, JC .
JOURNAL OF CHEMICAL ECOLOGY, 2004, 30 (07) :1363-1379
[7]   Peroxidase isozyme patterns in the skin of maturing tomato fruit [J].
Andrews, J ;
Malone, M ;
Thompson, DS ;
Ho, LC ;
Burton, KS .
PLANT CELL AND ENVIRONMENT, 2000, 23 (04) :415-422
[8]   Biochemical characterization of the suberization-associated anionic peroxidase of potato [J].
Bernards, MA ;
Fleming, WD ;
Llewellyn, DB ;
Priefer, R ;
Yang, XL ;
Sabatino, A ;
Plourde, GL .
PLANT PHYSIOLOGY, 1999, 121 (01) :135-145
[9]   Localized changes in peroxidase activity accompany hydrogen peroxide generation during the development of a nonhost hypersensitive reaction in lettuce [J].
Bestwick, CS ;
Brown, IR ;
Mansfield, JW .
PLANT PHYSIOLOGY, 1998, 118 (03) :1067-1078
[10]   A lignin-specific peroxidase in tobacco whose antisense suppression leads to vascular tissue modification [J].
Blee, KA ;
Choi, JW ;
O'Connell, AP ;
Schuch, W ;
Lewis, NG ;
Bolwell, GP .
PHYTOCHEMISTRY, 2003, 64 (01) :163-176