The Saccharomyces cerevisiae YPR184w gene encodes the glycogen debranching enzyme

被引:14
作者
Teste, MA [1 ]
Enjalbert, B [1 ]
Parrou, JL [1 ]
François, JM [1 ]
机构
[1] INRA, UR 792, Dept Genie Biochim & Alimentaire, UMR CNRS 5504,Ctr Bioingn Gilbert Durand, F-31077 Toulouse 04, France
关键词
glycogen; debranching enzyme; functional analysis; stress; Saccharomyces cerevisiae;
D O I
10.1016/S0378-1097(00)00468-7
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The YPR184w gene encodes a 1536-amino acid protein that is 34-39% identical to the mammal, Drosophila melanogaster and Caenorhabditis elegans glycogen debranching enzyme. The N-terminal part of the protein possesses the four conserved sequences of the alpha -amylase superfamily, while the C-terminal part displays 50% similarity with the C-terminal of other eukaryotic glycogen debranching enzymes. Reliable measurement of alpha -1,4-glucanotransferase and alpha -1,6-glucosidase activity of the yeast debranching enzyme was determined in strains overexpressing YPR184w. The alpha -1,4-glucanotransferase activity of a partially purified preparation of debranching enzyme preferentially transferred maltosyl units than maltotriosyl. Deletion of YPR184w prevents glycogen degradation, whereas overexpression had no effect on the rate of glycogen breakdown. In response to stress and growth conditions, the transcriptional control of YPR184w gene, renamed GDB1 (for Glycogen DeBranching gene), is strictly identical to that of other genes involved in glycogen metabolism. (C) 2000 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:105 / 110
页数:6
相关论文
共 39 条
[1]   DEBRANCHING ENZYME FROM RABBIT SKELETAL-MUSCLE - EVIDENCE FOR LOCATION OF 2 ACTIVE-CENTERS ON A SINGLE POLYPEPTIDE-CHAIN [J].
BATES, EJ ;
HEATON, GM ;
TAYLOR, C ;
KERNOHAN, JC ;
COHEN, P .
FEBS LETTERS, 1975, 58 (01) :181-185
[2]   THE YDP PLASMIDS - A UNIFORM SET OF VECTORS BEARING VERSATILE GENE DISRUPTION CASSETTES FOR SACCHAROMYCES-CEREVISIAE [J].
BERBEN, G ;
DUMONT, J ;
GILLIQUET, V ;
BOLLE, PA ;
HILGER, F .
YEAST, 1991, 7 (05) :475-477
[3]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[4]  
Brown DH, 1966, METHOD ENZYMOL, V8, P515, DOI 10.1016/0076-6879(66)08093-5
[5]   A SERIES OF YEAST SHUTTLE VECTORS FOR EXPRESSION OF CDNAS AND OTHER DNA-SEQUENCES [J].
BRUNELLI, JP ;
PALL, ML .
YEAST, 1993, 9 (12) :1299-1308
[6]  
CHEN YT, 1987, AM J HUM GENET, V41, P1002
[7]   THE CONTROL OF GLYCOGEN-METABOLISM IN YEAST .1. INTERCONVERSION INVIVO OF GLYCOGEN-SYNTHASE AND GLYCOGEN-PHOSPHORYLASE INDUCED BY GLUCOSE, A NITROGEN-SOURCE OR UNCOUPLERS [J].
FRANCOIS, J ;
VILLANUEVA, ME ;
HERS, HG .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1988, 174 (03) :551-559
[8]  
Francois J., 1997, YEAST SUGAR METABOLI, P285
[9]   AMYLO-1,6-GLUCOSIDASE-4-ALPHA-GLUCANOTRANSFERASE - USE OF REVERSIBLE SUBSTRATE MODEL INHIBITORS TO STUDY BINDING AND ACTIVE-SITES OF RABBIT MUSCLE DEBRANCHING ENZYME [J].
GILLARD, BK ;
NELSON, TE .
BIOCHEMISTRY, 1977, 16 (18) :3978-3987
[10]   DETERMINATION OF AMYLO-1,6-GLUCOSIDASE [J].
HERS, HG ;
VERHUE, W ;
VANHOOF, F .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1967, 2 (03) :257-+