Characteristics of digestive enzymes of calanoid copepod species from different latitudes in relation to temperature, pH and food

Comp Biochem Physiol B Biochem Mol Biol. 2012 Aug;162(4):66-72. doi: 10.1016/j.cbpb.2012.04.007. Epub 2012 Apr 26.

Abstract

In calanoid copepods it is poorly understood how enzymatic activities and patterns are affected by abiotic and biotic factors. Such knowledge, however, is crucial to assess metabolic functioning and performance of organisms in different habitats. Therefore, our study focuses on digestive enzyme activities in relation to temperature, pH and food in the Arctic species Calanus glacialis and in Centropages hamatus and Temora longicornis from the North Sea. Enzyme activities were measured over a range from 0 to 70 °C (lipases/esterases, proteinases) and pH 5 to 9 (proteinases). In all species, relative proteinases activity peaked at 40/50 °C and pH 6; relative lipases/esterases activity peaked at 30 °C. Between 0 and 20 °C, lipase activity of C. glacialis was higher (40-70% of maximum) than that of the boreal copepods (25-64%), which suggests thermal adaptation of the lipid metabolism in the polar species. Incubating C. glacialis with the diatom Thalassiosira weissflogii showed (i) that enzyme activities increased especially in the alkaline range and (ii) that enzyme patterns, revealed by gel electrophoresis, differed from that of starving individuals, indicating that feeding induced enzyme expression. Such studies, linking abiotic and biotic conditions to enzyme functioning, can help elucidating the capacity of copepods to respond to environmental changes.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptation, Physiological
  • Animal Nutritional Physiological Phenomena
  • Animals
  • Anthracenes
  • Copepoda / enzymology*
  • Copepoda / physiology
  • Digestive System / enzymology*
  • Eating
  • Ecosystem*
  • Esterases / metabolism*
  • Food
  • Hydrogen-Ion Concentration
  • Peptide Hydrolases / metabolism*
  • Species Specificity
  • Temperature

Substances

  • AnOV compound
  • Anthracenes
  • Esterases
  • Peptide Hydrolases