ENZYME-ACTIVITY PROFILES IN AN OVERWINTERING POPULATION OF FREEZE-TOLERANT LARVAE OF THE GALL FLY, EUROSTA-SOLIDAGINIS

被引:55
作者
JOANISSE, DR
STOREY, KB
机构
[1] CARLETON UNIV,INST BIOCHEM,OTTAWA K1S 5B6,ON,CANADA
[2] CARLETON UNIV,DEPT BIOL,OTTAWA K1S 5B6,ON,CANADA
关键词
INSECT FREEZE TOLERANCE; ENZYMES; METABOLISM; CRYOPROTECTANT SYNTHESIS; EUROSTA SOLIDAGINIS;
D O I
10.1007/BF00354086
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The activity of some enzymes of intermediary metabolism, including enzymes of glycolysis, the hexose monophosphate shunt, and polyol cryoprotectant synthesis, were measured in freeze-tolerant Eurosta solidaginis larvae over a winter season and upon entry into pupation. Flexible metabolic rearrangement was observed concurrently with acclimatization and development. Profiles of enzyme activities related to the metabolism of the cryoprotectant glycerol indicated that fall biosynthesis may occur from two possible pathways: 1. glyceraldehyde-phosphate --> glyceraldehyde --> glycerol, using glyceraldehyde phosphatase and NADPH-linked polyol dehydrogenase, or 2. dihydroxyacetone-phosphate --> glycerol-3-phosphate --> glycerol, using glycerol-3-phosphate dehydrogenase and glycerol-3-phosphatase. Clearance of glycerol in the spring appeared to occur by a novel route through the action of polyol dehydrogenase and glyceraldehyde kinase. Profiles of enzyme activities associated with sorbitol metabolism suggested that this polyol cryoprotectant was synthesized from glucose-6-phosphate through the action of glucose-6-phosphatase and NADPH-linked polyol dehydrogenase. Removal of sorbitol in the spring appeared to occur through the action of sorbitol dehydrogenase and hexokinase. Glycogen phosphorylase activation ensured the required flow of carbon into the synthesis of both glycerol and sorbitol. Little change was seen in the activity of glycolytic or hexose monophosphate shunt enzymes over the winter. Increased activity of the cl-glycerophosphate shuttle in the spring, indicated by greatly increased glycerol-3-phosphate dehydrogenase activity, may be key to removal and oxidation of reducing equivalents generated from polyol cryoprotectant catabolism.
引用
收藏
页码:247 / 255
页数:9
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