Glucose-6-phosphate dehydrogenase in cold hardy insects: Kinetic properties, freezing stabilization, and control of hexose monophosphate shunt activity
Properties of glucose-6-phosphate dehydrogenase were assessed from the larvae of three insect species, the freeze tolerant Eurosta solidaginis, the freeze avoiding Epiblema scudderiana, and warm-acclimated Tenebrio molitor. Maximal enzyme activities were 16-17 fold higher in the cold hardy larvae than in T. molitor in line with the key role of G6PDH in providing NADPH for the synthesis of cryoprotectant polyols in these species. Km values for glucose-6-P and NADP were determined at both high (24°C) and low (4°C) temperatures for all three enzymes. Temperature decrease had the greatest effect on T. molitor G6PDH increasing Km glucose-6-P by 3-fold and Km NADP by 2-fold; Km values for G6PDH from the cold hardy species were less temperature-sensitive. The addition of polyols (glycerol, sorbitol) or KCl caused selected changes in the Km values for both substrates in all species. Cryoprotectant action in the freezing protection of G6PDH was also examined, comparing G6PDH from E. solidaginis, E. scudderiana and yeast. A range of polyols (glycerol, sorbitol), other carbohydrates (trehalose, glucose, lactate) and amino acids (alanine, glutamate, proline) were effective in protecting activity during freezing. Without cryoprotectant, enzyme activity after 1 h freezing at -77°C was <10% compared to controls. Low concentrations of protectants (typically <50 mM) gave complete protection during freezing. Values for cryoprotectant concentrations giving half-maximal recovery of activity ranged from as low as 7-10 mM for trehalose to 20-25 mM for most other compounds.
|Keywords||cryoprotectants, Epiblema scudderiana, Eurosta solidaginis, freeze denaturation of enzymes, hexose monophosphate shunt, polyol synthesis, Tenebrio molitor|
Storey, K, Keefe, D. (Derrick), Kourtz, L. (Lauralynn), & Storey, J. (1991). Glucose-6-phosphate dehydrogenase in cold hardy insects: Kinetic properties, freezing stabilization, and control of hexose monophosphate shunt activity. Insect Biochemistry, 21(2), 157–164. doi:10.1016/0020-1790(91)90046-H