PROTON-TRANSPORT ACTIVITY, SIDEDNESS, AND MORPHOMETRY OF TONOPLAST AND PLASMA-MEMBRANE VESICLES PURIFIED BY FREE-FLOW ELECTROPHORESIS FROM ROOTS OF LEPIDIUM-SATIVUM L AND HYPOCOTYLS OF CUCURBITA-PEPO L

被引:9
作者
SCHERER, GFE
VOMDORP, B
SCHOLLMANN, C
VOLKMANN, D
机构
[1] Botanisches Institut, Universität Bonn, Bonn, 1
关键词
CUCURBITA; FILIPIN; H+-ATPASE; LEPIDIUM; PLASMA MEMBRANE; TONOPLAST;
D O I
10.1007/BF00198027
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Large-scale preparations of highly purified tonoplast and plasma-membrane vesicles were obtained from roots (garden cress, Lepidium sativum L.) and shoots (etiolated zucchini hypocotyl, Cucurbita pepo L.) of representative dicotyledonous seedlings. When tonoplast-enriched fractions of cress roots were prepared by centrifugation and then subjected to free-flow electrophoresis a highly purified tonoplast fraction was obtained. This fraction from cress roots was characterized by morphometry of filipin-treated freeze-fractured preparations and by enzymology to be about 90% homogeneous. Using latency of nitrate-inhibited ATPase and H+-pumping as criteria we found that the majority of the tonoplast vesicles from both sources were oriented right(cytoplasmic)-side-out. Plasma-membrane vesicles were first purified by two-phase partitioning and then subjected to free-flow electrophoresis for further purification. From cress roots, the fraction of highest purity contained 89% plasma-membrane vesicles as judged by morphometry of filipin-treated, freeze-fractured preparations and by enzymology. From both sources, the major plasma-membrane subfraction in the upper phase after two-phase partitioning was shown to have the least electrophoretic mobility in free-flow electrophoresis and to be oriented right(extracytoplasmic)-side-out a slightly more mobile plasma-membrane subfraction was oriented inside-out and originated after freezing thawing from outside-out plasma-membrane vesicles.
引用
收藏
页码:483 / 494
页数:12
相关论文
共 49 条
[11]  
CANUT H, 1990, PLANT PHYSIOL, V94, P1146
[12]   USE OF THE PYROPHOSPHATASE ACTIVITY AS A RELIABLE TONOPLAST MARKER IN MAIZE ROOTS [J].
CHANSON, A .
PLANT SCIENCE, 1990, 71 (02) :199-207
[13]  
CHURCHILL KA, 1983, PLANT PHYSIOL, V65, P921
[14]   IDENTIFICATION OF TONOPLAST FRACTIONS RESOLVED FROM PLASMA-MEMBRANE BY FREE-FLOW ELECTROPHORESIS USING FILIPIN-LABELING AND ANTIBODY TO THE TONOPLAST ATPASE [J].
DORP, BV ;
SCHERER, GFE ;
CANUT, H ;
BRIGHTMAN, AO ;
LIEDTKE, C ;
MORRE, DJ .
PROTOPLASMA, 1990, 156 (1-2) :57-66
[15]   PHOTOAFFINITY-LABELING AND PARTIAL-PURIFICATION OF THE PUTATIVE PLANT RECEPTOR FOR THE FUNGAL WILT-INDUCING TOXIN, FUSICOCCIN [J].
FEYERABEND, M ;
WEILER, EW .
PLANTA, 1989, 178 (03) :282-290
[16]   ACTIVATION OF 1,3-BETA-GLUCAN SYNTHASE BY CA-2+, SPERMINE AND CELLOBIOSE - LOCALIZATION OF ACTIVATOR SITES USING INSIDE-OUT PLASMA-MEMBRANE VESICLES [J].
FREDRIKSON, K ;
LARSSON, C .
PHYSIOLOGIA PLANTARUM, 1989, 77 (02) :196-201
[17]   GENERAL MECHANISMS FOR SOLUTE TRANSPORT ACROSS THE TONOPLAST OF PLANT VACUOLES - A PATCH-CLAMP SURVEY OF ION CHANNELS AND PROTON PUMPS [J].
HEDRICH, R ;
BARBIERBRYGOO, H ;
FELLE, H ;
FLUGGE, UI ;
LUTTGE, U ;
MAATHUIS, FJM ;
MARX, S ;
PRINS, HBA ;
RASCHKE, K ;
SCHNABL, H ;
SCHROEDER, JI ;
STRUVE, I ;
TAIZ, L ;
ZIEGLER, P .
BOTANICA ACTA, 1988, 101 (01) :7-13
[18]   SUBCELLULAR FRACTIONATION OF TISSUE-CULTURE CELLS [J].
HOWELL, KE ;
DEVANEY, E ;
GRUENBERG, J .
TRENDS IN BIOCHEMICAL SCIENCES, 1989, 14 (02) :44-47
[19]   INFLUENCE OF FREE FATTY-ACIDS, LYSOPHOSPHATIDYLCHOLINE, PLATELET-ACTIVATING-FACTOR, ACYLCARNITINE, AND ECHINOCANDIN-B ON 1,3-BETA-D-GLUCAN SYNTHASE AND CALLOSE SYNTHESIS [J].
KAUSS, H ;
JEBLICK, W .
PLANT PHYSIOLOGY, 1986, 80 (01) :7-13
[20]   INSIDE-OUT PLANT PLASMA-MEMBRANE VESICLES OF HIGH-PURITY OBTAINED BY AQUEOUS 2-PHASE PARTITIONING [J].
LARSSON, C ;
WIDELL, S ;
SOMMARIN, M .
FEBS LETTERS, 1988, 229 (02) :289-292