Characterization of three potato lipoxygenases with distinct enzymatic activities and different organ-specific and wound-regulated expression patterns

被引:192
作者
Royo, J
Vancanneyt, G
Perez, AG
Sanz, C
Stormann, K
Rosahl, S
SanchezSerrano, JJ
机构
[1] UNIV AUTONOMA MADRID, CSIC, CTR NACL BIOTECNOL, E-28049 MADRID, SPAIN
[2] CSIC, INST GRASA, E-41012 SEVILLE, SPAIN
[3] MAX PLANCK INST ZUCHTUNGSFORSCH, D-50829 COLOGNE, GERMANY
关键词
D O I
10.1074/jbc.271.35.21012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lipoxygenases are ubiquitous enzymes in eukaryotes. In plants, lipoxygenases are involved in the synthesis of the hormone jasmonic acid that regulates plant responses to wounding and, in addition, is an inducer of tuberization in potato. We have isolated potato lipoxygenase cDNA clones, From their deduced amino acid sequences, three distinct classes are defined (Lox1, Lox2, and Lox3), They are encoded in gene families that display organ-specific expression, lox1 being expressed mostly in tubers and roots, lox2 in leaves, and lox3 in leaves and roots. Consistent with their organ-specific expression pattern, Lox1 expressed in bacteria preferentially uses as substrate linoleic acid, abundant in membrane lipids of tubers, whereas linolenic acid, prevalent in leaves, is the preferred substrate for the other two classes of lipoxygenase. Analyses on reaction products of the enzymes expressed in bacteria reveal that Lox1 primarily produces 9-hydroperoxides. In contrast, the jasmonic acid precursor, 13-hydroperoxylinolenic acid, is the major product, of the action of Lox2 and Lox3 on linolenic acid. Upon wounding, the levels of Lox2 and Lox3 transcripts rise markedly in leaves. While Lox3 mRNA accumulation peaks as early as 30 min after wounding, Lox2 shows a steady increase over a 24-h time course, suggesting different roles for these Lipoxygenase isoforms in the synthesis of the plant hormone jasmonic acid.
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页码:21012 / 21019
页数:8
相关论文
共 43 条
[1]   CHARACTERIZATION OF AN ARABIDOPSIS-LIPOXYGENASE GENE RESPONSIVE TO METHYL JASMONATE AND WOUNDING [J].
BELL, E ;
MULLET, JE .
PLANT PHYSIOLOGY, 1993, 103 (04) :1133-1137
[2]   A CHLOROPLAST LIPOXYGENASE IS REQUIRED FOR WOUND-INDUCED JASMONIC ACID ACCUMULATION IN ARABIDOPSIS [J].
BELL, E ;
CREELMAN, RA ;
MULLET, JE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (19) :8675-8679
[3]   Envelope membranes from spinach chloroplasts are a site of metabolism of fatty acid hydroperoxides [J].
Blee, E ;
Joyard, J .
PLANT PHYSIOLOGY, 1996, 110 (02) :445-454
[4]   RAPID STIMULATION OF 5-LIPOXYGENASE ACTIVITY IN POTATO BY THE FUNGAL ELICITOR ARACHIDONIC-ACID [J].
BOSTOCK, RM ;
YAMAMOTO, H ;
CHOI, D ;
RICKER, KE ;
WARD, BL .
PLANT PHYSIOLOGY, 1992, 100 (03) :1448-1456
[5]   THE 3-DIMENSIONAL STRUCTURE OF AN ARACHIDONIC-ACID 15-LIPOXYGENASE [J].
BOYINGTON, JC ;
GAFFNEY, BJ ;
AMZEL, LM .
SCIENCE, 1993, 260 (5113) :1482-1486
[6]   SEQUENCE OF A CDNA CLONE ENCODING A POTATO (SOLANUM-TUBEROSUM) TUBER LIPOXYGENASE [J].
CASEY, R .
PLANT PHYSIOLOGY, 1995, 107 (01) :265-266
[7]   TUBERIZATION IN THE POTATO PLANT [J].
CHAPMAN, HW .
PHYSIOLOGIA PLANTARUM, 1958, 11 (02) :215-224
[8]   CONVENIENT APPARATUS FOR THE GENERATION OF SMALL AMOUNTS OF DIAZOMETHANE [J].
COHEN, JD .
JOURNAL OF CHROMATOGRAPHY, 1984, 303 (01) :193-196
[9]   VOLATILE PRODUCTS OF THE LIPOXYGENASE PATHWAY EVOLVED FROM PHASEOLUS-VULGARIS (L) LEAVES INOCULATED WITH PSEUDOMONAS-SYRINGAE PV-PHASEOLICOLA [J].
CROFT, KPC ;
JUTTNER, F ;
SLUSARENKO, AJ .
PLANT PHYSIOLOGY, 1993, 101 (01) :13-24
[10]   IMPROVED CATHODE FOR MEASUREMENT OF PHOTOSYNTHETIC OXYGEN EVOLUTION BY ISOLATED CHLOROPLASTS [J].
DELIEU, T ;
WALKER, DA .
NEW PHYTOLOGIST, 1972, 71 (02) :201-&