Ascorbate oxidase, protein disulfide isomerase, ascorbic acid, dehydroascorbic acid and protein levels in developing wheat kernels and their relationship to protein disulfide bond formation

被引:19
作者
Every, D [1 ]
Griffin, WB [1 ]
Wilson, PE [1 ]
机构
[1] New Zealand Inst Crop & Food Res, Grain Foods Res Unit, Christchurch, New Zealand
关键词
D O I
10.1094/CCHEM.2003.80.1.35
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Developing wheat kernels of three New Zealand wheat cultivars; at one to nine weeks postanthesis (WPA) were analyzed for kernel weight, salt-soluble protein, salt-insoluble protein, ascorbate oxidase (AOX), protein disulfide isomerase (PDI), ascorbic acid (AA), and dehydroascorbic acid (DHA). Kernel weight and salt-soluble protein increased from one to five or six WPA then declined. The amount of salt-insoluble protein per kernel rapidly increased from two to five or six WPA, then remained constant. AOX activity increased from one to two or three WPA then declined to almost zero at seven WPA. PDI activity increased from one to three WPA, stayed constant to six WPA, then declined about 25%. DHA increased from one to two or three WPA then declined to zero at seven WPA. AA increased from one to three or five WPA then declined to zero at seven WPA. When DHA, at similar concentrations (approximate to1 mM) to that found in one to six WPA kernels, was mixed with reduced-gluten proteins, it was reduced to AA. The results are interpreted as a scheme showing that, during the formation of protein-disulfide bonds, electrons are transferred from nascent protein thiols, ultimately to oxygen, through a series of electron carriers including PDI, AA-DHA, and AOX.
引用
收藏
页码:35 / 39
页数:5
相关论文
共 38 条
[21]   REDOX PROPERTIES AND CROSS-LINKING OF THE DITHIOL DISULFIDE ACTIVE-SITES OF MAMMALIAN PROTEIN DISULFIDE-ISOMERASE [J].
HAWKINS, HC ;
DENARDI, M ;
FREEDMAN, RB .
BIOCHEMICAL JOURNAL, 1991, 275 :341-348
[22]   Transport and action of ascorbate at the plant plasma membrane [J].
Horemans, N ;
Foyer, CH ;
Asard, H .
TRENDS IN PLANT SCIENCE, 2000, 5 (06) :263-267
[23]  
Kasarda DD, 1999, CEREAL FOOD WORLD, V44, P566
[24]   CATALYSIS OF THE OXIDATIVE FOLDING OF RIBONUCLEASE-A BY PROTEIN DISULFIDE ISOMERASE - DEPENDENCE OF THE RATE ON THE COMPOSITION OF THE REDOX BUFFER [J].
LYLES, MM ;
GILBERT, HF .
BIOCHEMISTRY, 1991, 30 (03) :613-619
[25]   Hut1 proteins identified in Saccharomyces cerevisiae and Schizosaccharomyces pombe are functional homologues involved in the protein-folding process at the endoplasmic reticulum [J].
Nakanishi, H ;
Nakayama, K ;
Yokota, A ;
Tachikawa, H ;
Takahashi, N ;
Jigami, Y .
YEAST, 2001, 18 (06) :543-554
[26]   Protein-disulfide isomerase- and protein thiol-dependent dehydroascorbate reduction and ascorbate accumulation in the lumen of the endoplasmic reticulum [J].
Nardai, G ;
Braun, L ;
Csala, M ;
Mile, V ;
Csermely, P ;
Benedetti, A ;
Mandl, J ;
Bánhegyi, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (12) :8825-8828
[27]  
Osborne TB., 1907, The proteins of wheat kernel
[28]  
PANOZZO JF, 1996, P 6 INT GLUT WORKSH, P477
[29]   PROTEIN DISULFIDE-ISOMERASE IS LOCATED IN THE ENDOPLASMIC-RETICULUM OF DEVELOPING WHEAT ENDOSPERM [J].
RODEN, LT ;
MIFLIN, BJ ;
FREEDMAN, RB .
FEBS LETTERS, 1982, 138 (01) :121-124
[30]  
Shewry PR, 1999, CEREAL FOOD WORLD, V44, P587