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author Schmithüsen, Tosia
Niehoff, Barbara
Auel, Holger
author_facet Schmithüsen, Tosia
Niehoff, Barbara
Auel, Holger
collection Datos científicos de ciencias marinas y ambientales
contents The activities of proteinases, lipases/esterases and citrate synthase of Calanus finmarchicus copepodites (CV) were analysed. Analysis was performed at 30°C for copepods from seven stations (126-9, 127-17, 131-17, 133-6, 134-19, 135-16, 136-8). In addition, thermal profiles (5-50°C) of these enzymes were analysed for copepods from 3 stations (127-17, 133-6, 135-16). C. finmarchicus of station 127-19 have been acclimated on board to two different temperatures (4 and 15°C) for two weeks. Thermal profiles (5-60°C) of lipases/esterases and proteinases of adult females from each treatment were analysed. Groups of 10 individuals were used to prepare enzyme extracts for analysis. From each station/treatment, three groups were analysed, each of which was measured in triplicates. The activity of proteinases was determined photometrically after Saborowski et al. (2004, hdl:10013/epic.20836), modified after Kreibich et al. (2008, doi:10.1007/s10152-008-0112-0). Azocasein was used as substrate. The lypolytic activity of lipases and esterases in the extract was analysed fluorometrically after Knotz et al. (2006, doi:10.1016/j.cbpa.2006.07.019) using 4-methylumbelliferyl butyrate as substrate. Citrate synthase activity was analysed photometrically after Stitt (1984) modified by Saborowski and Buchholz (2002) with oxaloacetic acid as substrate. For detailed description please contact the author.
format Dataset Open Access
id pangaea_https___doi_org_10_1594_PANGAEA_835177
institution PANGAEA
language en
publishDate 2014
publisher PANGAEA
record_format pangaea
spellingShingle Enzyme activities of Calanus finmarchicus from the North Atlantic collected during Maria S. Merian cruise MSM26 in spring 2013
Schmithüsen, Tosia
Niehoff, Barbara
Auel, Holger
Absorbance of control; Absorbance of sample; Basin Scale Analysis, Synthesis and Integration; Citrate synthase activity, dry mass; Citrate synthase activity per individual; Date; Date/Time of event; Depth, bottom/max; Depth, top/min; DEPTH, water; D-MOC; Double opening/closing plankton net; EURO-BASIN; Event label; Latitude of event; Life stage; Lipase activity, dry mass; Lipase activity per individual; Longitude of event; Maria S. Merian; MSM26; MSM26_126-9; MSM26_127-17; MSM26_127-19; MSM26_131-17; MSM26_133-6; MSM26_134-19; MSM26_135-16; MSM26_136-8; North Atlantic Ocean; Number of individuals; Proteinase activity, per dry mass, Delta extinction at 366 nm; Proteinase activity per individual, Delta extinction at 366 nm; Sample ID; Spectrophotometer Thermo Scientific UV1; Taxon/taxa; Treatment; Treatment: temperature; Uniform resource locator/link to reference; WP2; WP-2 towed closing plankton net
The activities of proteinases, lipases/esterases and citrate synthase of Calanus finmarchicus copepodites (CV) were analysed. Analysis was performed at 30°C for copepods from seven stations (126-9, 127-17, 131-17, 133-6, 134-19, 135-16, 136-8). In addition, thermal profiles (5-50°C) of these enzymes were analysed for copepods from 3 stations (127-17, 133-6, 135-16). C. finmarchicus of station 127-19 have been acclimated on board to two different temperatures (4 and 15°C) for two weeks. Thermal profiles (5-60°C) of lipases/esterases and proteinases of adult females from each treatment were analysed. Groups of 10 individuals were used to prepare enzyme extracts for analysis. From each station/treatment, three groups were analysed, each of which was measured in triplicates. The activity of proteinases was determined photometrically after Saborowski et al. (2004, hdl:10013/epic.20836), modified after Kreibich et al. (2008, doi:10.1007/s10152-008-0112-0). Azocasein was used as substrate. The lypolytic activity of lipases and esterases in the extract was analysed fluorometrically after Knotz et al. (2006, doi:10.1016/j.cbpa.2006.07.019) using 4-methylumbelliferyl butyrate as substrate. Citrate synthase activity was analysed photometrically after Stitt (1984) modified by Saborowski and Buchholz (2002) with oxaloacetic acid as substrate. For detailed description please contact the author.
title Enzyme activities of Calanus finmarchicus from the North Atlantic collected during Maria S. Merian cruise MSM26 in spring 2013
topic Absorbance of control; Absorbance of sample; Basin Scale Analysis, Synthesis and Integration; Citrate synthase activity, dry mass; Citrate synthase activity per individual; Date; Date/Time of event; Depth, bottom/max; Depth, top/min; DEPTH, water; D-MOC; Double opening/closing plankton net; EURO-BASIN; Event label; Latitude of event; Life stage; Lipase activity, dry mass; Lipase activity per individual; Longitude of event; Maria S. Merian; MSM26; MSM26_126-9; MSM26_127-17; MSM26_127-19; MSM26_131-17; MSM26_133-6; MSM26_134-19; MSM26_135-16; MSM26_136-8; North Atlantic Ocean; Number of individuals; Proteinase activity, per dry mass, Delta extinction at 366 nm; Proteinase activity per individual, Delta extinction at 366 nm; Sample ID; Spectrophotometer Thermo Scientific UV1; Taxon/taxa; Treatment; Treatment: temperature; Uniform resource locator/link to reference; WP2; WP-2 towed closing plankton net
url https://doi.org/10.1594/PANGAEA.835177