Differences in the activity and distribution of peroxidases from three different portions of germinating Brassica oleracea seeds

被引:21
作者
Bellani, LM
Guarnieri, M
Scialabba, A
机构
[1] Univ Palermo, Dipartimento Sci Bot, I-90123 Palermo, Italy
[2] Univ Siena, Dipartimento Biol Evolut, I-53100 Siena, Italy
[3] Univ Siena, Ctr Servizi, Fac Sci, I-53100 Siena, Italy
关键词
D O I
10.1034/j.1399-3054.2002.1140114.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Peroxidase (POD, EC 1.11.1.7) activity, cellular localization and isozyme patterns were investigated in the seed integument, cotyledon and embryo axis of Brassica oleracea cv. Cappuccio during pregermination and seedling growth. Seeds started to germinate after 24 h of imbibition. POD activity was localized in the pigmented layer of the integument and in procambial strands of the cotyledon and embryo axis in the first 24 h of imbibition. It was localized in the integumental cells of palisade, pigmented and aleurone layers and in epidermal, meristematic, procambial cells and xylem elements of the root and hypocotyl after 48 h of imbibition. POD activity increased during germination and early seedling growth: in the integument, it reached a maximum value after 72 h of imbibition, in the embryo axis and cotyledons, it increased up to 144 h of imbibition. The increase in peroxidase activity was accompanied by the appearance of new isozymes correlated with the development of seedling tissues. The isozyme profile was characterized by nine peroxidases: isoperoxidase of 50 kDa peculiar to integuments, that of 150 kDa to cotyledons and that of 82 kDa to the embryo axis. During pregerminative phase isozymes of 84 kDa were detected in the integument and cotyledons, of 48.5 kDa in the embryo axis. After germination, peroxidase activity and the complexity of the isozyme pattern increased, suggesting that they play a relevant role after rupture of the integument.
引用
收藏
页码:102 / 108
页数:7
相关论文
共 35 条
[1]  
ANGELINI R, 1990, PLANTA, V182, P89, DOI 10.1007/BF00239989
[2]  
BELLANI LM, 2000, INF BOT ITAL, V32, P85
[3]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[4]   ELICITATION OF LIGNIN BIOSYNTHESIS AND ISOPEROXIDASE ACTIVITY BY PECTIC FRAGMENTS IN SUSPENSION-CULTURES OF CASTOR BEAN [J].
BRUCE, RJ ;
WEST, CA .
PLANT PHYSIOLOGY, 1989, 91 (03) :889-897
[5]   PEROXIDASE RELEASE INDUCED BY OZONE IN SEDUM-ALBUM LEAVES INVOLVEMENT OF CA-2+ [J].
CASTILLO, FJ ;
PENEL, C ;
GREPPIN, H .
PLANT PHYSIOLOGY, 1984, 74 (04) :846-851
[6]  
Catesson A. M., 1986, MOL PHYSL ASPECTS PL, P189
[7]  
CELLA R, 1997, PLANT PEROXIDASE NEW
[8]   THE HEME MOIETY IN PEANUT PEROXIDASE [J].
CHIBBAR, RN ;
CELLA, R ;
VANHUYSTEE, RB .
CANADIAN JOURNAL OF BIOCHEMISTRY AND CELL BIOLOGY, 1984, 62 (11) :1046-1050
[9]   The induction of soluble peroxidase activity in bean leaves by wind-induced mechanical perturbation [J].
Cipollini, DF .
AMERICAN JOURNAL OF BOTANY, 1998, 85 (11) :1586-1591
[10]   ROLE OF PEROXIDASE IN THE DEVELOPMENT OF WATER-IMPERMEABLE SEED COATS IN SIDA-SPINOSA L [J].
EGLEY, GH ;
PAUL, RN ;
VAUGHN, KC ;
DUKE, SO .
PLANTA, 1983, 157 (03) :224-232