Cabbage cryoprotectin is a member of the nonspecific plant lipid transfer protein gene family

被引:33
作者
Hincha, DK
Neukamm, B
Sror, HAM
Sieg, F
Weckwarth, W
Rückels, M
Lullien-Pellerin, V
Schröder, W
Schmitt, JM
机构
[1] Free Univ Berlin, Inst Pflanzenphysiol & Mikrobiol, D-14195 Berlin, Germany
[2] Max Planck Inst Mol Pflanzenphysiol, D-14424 Potsdam, Germany
[3] Boehringer Mannheim GmbH, Abt BPZ 6, Div Biochem, D-82372 Penzberg, Germany
[4] INRA, Unite Biochim & Biol Mol Cereales, F-34060 Montpellier 01, France
[5] Free Univ Berlin, Inst Biochem, SFB 344, D-14195 Berlin, Germany
关键词
D O I
10.1104/pp.125.2.835
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
We have recently purified a protein (cryoprotectin) from the leaves of: cold-acclimated cabbage (Brassica oleracea) to electrophoretic homogeneity, which protects thylakoids isolated from the leaves of nonacclimated spinach (Spinacia oleracea) from freeze-thaw damage. Sequencing of cryoprotectin showed the presence of at least three isoforms of WAX9 proteins, which belong to the class of nonspecific lipid transfer proteins. Antibodies raised against two synthetic peptides derived from the WAX9 proteins recognized a band of approximately 10 kD in western blots of crude cryoprotectin preparations. This protein and the cryoprotective activity could be precipitated from solution by the antiserum. We show further that cryoprotectin is structurally and functionally different from WAX9 isolated from the surface wax of cabbage leaves. WAX9 has lipid transfer activity for phosphatidylcholine, but no cryoprotective activity. Cryoprotectin, on the other hand, has cryoprotective, but no lipid transfer activity. The cryoprotective activity of cryoprotectin was strictly dependent on Ca2+ and Mn2+ and could be inhibited by chelating agents, whereas the lipid transfer activity of WAX9 was higher in the presence of ethylenediaminetetraacetate than in the presence of Ca2+ and Mn2+.
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页码:835 / 846
页数:12
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