2 CLASSES OF STARCH DEBRANCHING ENZYMES FROM DEVELOPING MAIZE KERNELS

被引:44
作者
DOEHLERT, DC
KNUTSON, CA
机构
[1] United States Department of Agriculture, Agricultural Research Service, National Center for Agricultural Utilization Research, Seed Biosynthesis Research Unit, Peoria, Illinois, 61604
关键词
ZEA-MAYS L; PULLULANASE; ISOAMYLASE; STARCH HYDROLYSIS;
D O I
10.1016/S0176-1617(11)80242-7
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Based on their substrate specificities, two distinct classes of starch debranching enzymes have been isolated from developing maize kernels. One class of enzyme hydrolyzed pullulan most rapidly followed by beta-limit dextrin, amylopectin, and phytoglycogen. This activity was classified as a pullulanase (E.C. # 3.2.1.41). A different class of enzyme debranched amylopectin most rapidly, followed by beta-limit dextrin and phytoglycogen. It, however, would not hydrolyze pullulan and was classified as isoamylase (E.C. # 3.2.1.68). Two forms of isoamylase were isolated which differed in relative molecular mass and eluted separately on anion exchange chromatography, but only one form was characterized. Both classes of enzyme activity caused an increase in starch-iodine staining when incubated in an amylopectin solution. The optimal pH for pullulanase activity was pH 5.5, whereas isoamylase had optimal activity at pH 6.0 to 7.5. Both classes of enzyme required 5 mM dithiothreitol or the equivalent sulfhydryl reducing power for activity. We speculate that pullulanase may be specialized to function in conjunction with beta-amylase in hydrolyzing exposed alpha-1,6 branches, whereas isoamylase appears to be more efficient at hydrolyzing less exposed branches in amylopectin.
引用
收藏
页码:566 / 572
页数:7
相关论文
共 18 条
[1]   PHYSICOCHEMICAL STUDIES ON STARCHES .56. INTERACTION OF LINEAR, AMYLOSE OLIGOMERS WITH IODINE [J].
BANKS, W ;
GREENWOOD, CT ;
KHAN, KM .
CARBOHYDRATE RESEARCH, 1971, 17 (01) :25-+
[2]   BIOSYNTHESIS AND DEGRADATION OF STARCH IN HIGHER-PLANTS [J].
BECK, E ;
ZIEGLER, P .
ANNUAL REVIEW OF PLANT PHYSIOLOGY AND PLANT MOLECULAR BIOLOGY, 1989, 40 :95-117
[3]  
BERNFELD P, 1951, ADV ENZYMOL REL S BI, V12, P379
[4]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[5]   SPECIFIC DETERMINATION OF ALPHA-AMYLASE ACTIVITY IN CRUDE PLANT-EXTRACTS CONTAINING BETA-AMYLASE [J].
DOEHLERT, DC ;
DUKE, SH .
PLANT PHYSIOLOGY, 1983, 71 (02) :229-234
[6]   REVISION OF MEYER-BERNFELD MODEL OF GLYCOGEN AND AMYLOPECTIN [J].
GUNJASMITH, Z ;
MARSHALL, JJ ;
MERCIER, C ;
SMITH, EE ;
WHELAN, WJ .
FEBS LETTERS, 1970, 12 (02) :101-+
[7]  
HODGE JE, 1962, METHODS CARBOHYDRATE, V1, P388
[8]   DEBRANCHING ENZYMES OF POTATO-TUBERS (SOLANUM-TUBEROSUM-L) .1. PURIFICATION AND SOME PROPERTIES OF POTATO ISOAMYLASE [J].
ISHIZAKI, Y ;
TANIGUCHI, H ;
MARUYAMA, Y ;
NAKAMURA, M .
AGRICULTURAL AND BIOLOGICAL CHEMISTRY, 1983, 47 (04) :771-779
[9]   PURIFICATION AND SOME PROPERTIES OF DEBRANCHING ENZYME OF GERMINATING RICE ENDOSPERM [J].
IWAKI, K ;
FUWA, H .
AGRICULTURAL AND BIOLOGICAL CHEMISTRY, 1981, 45 (12) :2683-2688
[10]   SUBSTRATE SPECIFICITY OF AMYLOPECTIN-DEBRANCHING ENZYMES FROM SWEET CORN [J].
LEE, EYC ;
MARSHALL, JJ ;
WHELAN, WJ .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1971, 143 (02) :365-&