TOPOLOGICAL STUDIES OF SPINACH 22 KDA PROTEIN OF PHOTOSYSTEM-II

被引:27
作者
KIM, S
PICHERSKY, E
YOCUM, CF
机构
[1] UNIV MICHIGAN,DEPT BIOL,ANN ARBOR,MI 48109
[2] UNIV MICHIGAN,DEPT CHEM,ANN ARBOR,MI 48109
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | 1994年 / 1188卷 / 03期
关键词
PHOTOSYNTHESIS; MEMBRANE PROTEIN; POLYPEPTIDE; 22; KDA; WESTERN BLOT; TRYPSIN;
D O I
10.1016/0005-2728(94)90054-X
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
An intrinsic 22 kDa polypeptide is associated with the O-2-evolving Photosystem II core complex in a variety of green plants, although it does not appear to be required for O-2 evolution. Digestion of thylakoid membranes and isolated Photosystem II preparations with trypsin, followed by immunoblotting using spinach anti-22 kDa antibodies, leads to two observations: (1) the domain between the 2nd and 3rd transmembrane helices of the 22 kDa protein is stromally exposed, and (2) only in a reaction center complex preparation, lacking the chlorophyll a/b-light harvesting complex II, is there extensive protoelytic cleavage of the 22 kDa protein. We also found that after, but not prior to, selective extraction of the 22 and 10 kDa proteins from Photosystem II membranes, the chlorophyll a/b-light harvesting complex II can be separated from the Photosystem II reaction center core by precipitation with MgCl2. This result suggests that the 22 kDa polypeptide is located between the Photosystem II reaction center polypeptides and light-harvesting complex II; it is possible that the protein serves as a link between the two protein complexes. The presence of the 22 kDa protein in several species was also examined by immunoblotting with polyclonal spinach anti-22 kDa antibodies.
引用
收藏
页码:339 / 348
页数:10
相关论文
共 40 条
[1]   RECONSTITUTION OF PHOTOSYNTHETIC WATER SPLITTING IN INSIDE-OUT THYLAKOID VESICLES AND IDENTIFICATION OF A PARTICIPATING POLYPEPTIDE [J].
AKERLUND, HE ;
JANSSON, C ;
ANDERSSON, B .
BIOCHIMICA ET BIOPHYSICA ACTA, 1982, 681 (01) :1-10
[2]   COPPER ENZYMES IN ISOLATED CHLOROPLASTS - POLYPHENOLOXIDASE IN BETA-VULGARIS [J].
ARNON, DI .
PLANT PHYSIOLOGY, 1949, 24 (01) :1-15
[3]   CHLOROPLAST GRANA MEMBRANE CARBOXYL GROUPS - THEIR INVOLVEMENT IN MEMBRANE ASSOCIATION [J].
BERG, S ;
DODGE, S ;
KROGMANN, DW ;
DILLEY, RA .
PLANT PHYSIOLOGY, 1974, 53 (04) :619-627
[4]   A HIGHLY RESOLVED, OXYGEN-EVOLVING PHOTOSYSTEM-II PREPARATION FROM SPINACH THYLAKOID MEMBRANES - ELECTRON-PARAMAGNETIC-RES AND ELECTRON-TRANSPORT PROPERTIES [J].
BERTHOLD, DA ;
BABCOCK, GT ;
YOCUM, CF .
FEBS LETTERS, 1981, 134 (02) :231-234
[5]   EFFECTS OF CHOLATE ON PHOTOSYSTEM-II - SELECTIVE EXTRACTION OF A 22 KDA POLYPEPTIDE AND MODIFICATION OF Q(B)-SITE ACTIVITY [J].
BOWLBY, NR ;
YOCUM, CF .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1144 (03) :271-277
[6]   ANALYSIS OF THE LIGHT-HARVESTING PIGMENT-PROTEIN COMPLEX OF WILD-TYPE AND A CHLOROPHYLL-B-LESS MUTANT OF BARLEY [J].
BURKE, JJ ;
STEINBACK, KE ;
ARNTZEN, CJ .
PLANT PHYSIOLOGY, 1979, 63 (02) :237-243
[7]   INVOLVEMENT OF LIGHT-HARVESTING COMPLEX IN CATION REGULATION OF EXCITATION-ENERGY DISTRIBUTION IN CHLOROPLASTS [J].
BURKE, JJ ;
DITTO, CL ;
ARNTZEN, CJ .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1978, 187 (01) :252-263
[8]  
BURNETTE WN, 1981, ANAL BIOCHEM, V112, P195, DOI 10.1016/0003-2697(81)90281-5
[9]   THE RESOLUTION OF CHLOROPHYLL A/B BINDING-PROTEINS BY A PREPARATIVE METHOD BASED ON FLAT BED ISOELECTRIC-FOCUSING [J].
DAINESE, P ;
HOYERHANSEN, G ;
BASSI, R .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1990, 51 (06) :693-703
[10]   THE INTRINSIC 22 KDA PROTEIN IS A CHLOROPHYLL-BINDING SUBUNIT OF PHOTOSYSTEM-II [J].
FUNK, C ;
SCHRODER, WP ;
GREEN, BR ;
RENGER, G ;
ANDERSSON, B .
FEBS LETTERS, 1994, 342 (03) :261-266