STRUCTURAL-ANALYSIS OF THE CARBOHYDRATE MOIETY OF ARABINOGALACTAN-PROTEINS FROM STIGMAS AND STYLES OF NICOTIANA-ALATA

被引:100
作者
GANE, AM
CRAIK, D
MUNRO, SLA
HOWLETT, GJ
CLARKE, AE
BACIC, A
机构
[1] UNIV MELBOURNE,SCH BOT,PLANT CELL BIOL RES CTR,PARKVILLE,VIC 3052,AUSTRALIA
[2] MONASH UNIV,VICTORIAN COLL PHARM,PARKVILLE,VIC 3052,AUSTRALIA
[3] UNIV MELBOURNE,DEPT BIOCHEM,PARKVILLE,VIC 3052,AUSTRALIA
基金
澳大利亚研究理事会;
关键词
ARABINOGALACTAN-PROTEINS; STRUCTURAL ANALYSIS; NICOTRIANA ALATA;
D O I
10.1016/0008-6215(95)00197-2
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
Arabinogalactan-proteins (AGPs) from the female reproductive tissues (stigmas acid styles) of Nicotiana alata were isolated from the saturated ammonium sulfate supernatant of buffer-soluble extracts by precipitation with the beta-glucosyl Yariv reagent, followed by gel-filtration chromatography under dissociating conditions, The AGPs had characteristics typical of other AGPs: a high proportion of carbohydrate (95%) with a high ratio of Galp to Araf (2:1), and a low protein content (5%) with high levels of alanine, serine, and hydroxyproline. The AGPs consisted of a major species which was almost neutral, and a minor species which was more negatively charged. Sedimentation equilibrium experiments showed that the purified AGPs had a weight-average molecular weight of 143 kD. Linkage analysis showed that the AGPs contained a highly branched backbone of 3-, 6-, and 3,6-linked Galp residues, bearing terminal Galp and terminal Araf residues. Analysis by one-dimensional and two-dimensional H-1 and C-13 NMR spectroscopy confirmed the presence of these glycosyl linkage types, and showed a high mobility of the terminal Araf residues consistent with their location on the periphery of the molecules. This analysis represents the most complete H-1 assignment for AGP molecules in solution. No difference in the carbohydrate analyses was found between AGPs isolated separately from stigmatic or stylar tissue, or between AGPs isolated from stigmas and styles of plants of different self-incompatibility genotypes.
引用
收藏
页码:67 / 85
页数:19
相关论文
共 62 条
[1]   AN EXTRACELLULAR ARABINOGALACTAN-PROTEIN FROM NICOTIANA-TABACUM [J].
AKIYAMA, Y ;
KATO, K .
PHYTOCHEMISTRY, 1981, 20 (11) :2507-2510
[2]   SEQUENCE VARIABILITY OF 3 ALLELES OF THE SELF-INCOMPATIBILITY GENE OF NICOTIANA-ALATA [J].
ANDERSON, MA ;
MCFADDEN, GI ;
BERNATZKY, R ;
ATKINSON, A ;
ORPIN, T ;
DEDMAN, H ;
TREGEAR, G ;
FERNLEY, R ;
CLARKE, AE .
PLANT CELL, 1989, 1 (05) :483-491
[3]   CARBOHYDRATE-BINDING ARABINOGALACTAN-PROTEIN FROM LIQUID SUSPENSION CULTURES OF ENDOSPERM FROM LOLIUM-MULTIFLORUM [J].
ANDERSON, RL ;
CLARKE, AE ;
JERMYN, MA ;
KNOX, RB ;
STONE, BA .
AUSTRALIAN JOURNAL OF PLANT PHYSIOLOGY, 1977, 4 (01) :143-158
[4]   POLYSACCHARIDE COMPONENT IN STIGMATIC EXUDATE FROM LILIUM-LONGIFLORUM [J].
ASPINALL, GO ;
ROSELL, KG .
PHYTOCHEMISTRY, 1978, 17 (05) :919-922
[5]   PROTEINASE-INHIBITORS IN NICOTIANA-ALATA STIGMAS ARE DERIVED FROM A PRECURSOR PROTEIN WHICH IS PROCESSED INTO 5 HOMOLOGOUS INHIBITORS [J].
ATKINSON, AH ;
HEATH, RL ;
SIMPSON, RJ ;
CLARKE, AE ;
ANDERSON, MA .
PLANT CELL, 1993, 5 (02) :203-213
[6]   ARABINOGALACTAN PROTEINS FROM STIGMAS OF NICOTIANA-ALATA [J].
BACIC, A ;
GELL, AC ;
CLARKE, AE .
PHYTOCHEMISTRY, 1988, 27 (03) :679-684
[7]   FINE-STRUCTURE OF THE ARABINOGALACTAN PROTEIN FROM LOLIUM-MULTIFLORUM [J].
BACIC, A ;
CHURMS, SC ;
STEPHEN, AM ;
COHEN, PB ;
FINCHER, GB .
CARBOHYDRATE RESEARCH, 1987, 162 (01) :85-93
[8]   RAPID ANALYSIS OF AMINO-ACIDS USING PRE-COLUMN DERIVATIZATION [J].
BIDLINGMEYER, BA ;
COHEN, SA ;
TARVIN, TL .
JOURNAL OF CHROMATOGRAPHY, 1984, 336 (01) :93-104
[9]   NATURAL ABUNDANCE N-15 NMR BY ENHANCED HETERONUCLEAR SPECTROSCOPY [J].
BODENHAUSEN, G ;
RUBEN, DJ .
CHEMICAL PHYSICS LETTERS, 1980, 69 (01) :185-189
[10]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3