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1.
Biomolecules ; 9(6)2019 06 12.
Article in English | MEDLINE | ID: mdl-31212771

ABSTRACT

A protease from neon flying squid (Ommastrephes bartramii) viscera (SVCE3(f)) was partially purified by isoelectric solubilization/precipitation combined with ultra-membrane filtration (ISP-UMF). Two protein bands of 45 and 27 KDa were determined by SDS-PAGE assay. The protease characteristic of the protein band of 45 KDa was confirmed using casein zymography analysis. The result of UPLC-ESI-MS/MS suggested that the band of 45 KDa could be a cathepsin D-like protease. This cathepsin D-like protease showed an optimum pH of 3.0 and optimum temperature of 60 °C when casein was used as s substrate. Furthermore, its protease activity was stable at 30-50 °C and under a pH range of 1.0-5.0, maintaining about 60% of its initial activity. SVCE3(f) can digest half-fin anchovy (Setipinna taty) to generate antioxidant hydrolysates (HAHp-SEs). The degree of hydrolysis (DH) of HAHp-SEs increased along with the hydrolysis time and reached stability after 60 min of digestion. HAHp-SEs(30) with relatively lower DH exhibited the highest DPPH radical scavenging activity as compared with other HAHp-SEs. However, a stronger hydroxyl radical scavenging activity and greater reducing power were observed for HAHp-SEs that underwent higher DH. Accordingly, the partially purified cathepsin D-like protease of neon flying squid viscera using ISP-UMF could have potential application in antioxidant hydrolysates production.


Subject(s)
Antioxidants/metabolism , Cathepsin D/isolation & purification , Cathepsin D/metabolism , Cephalopoda/enzymology , Viscera/enzymology , Amino Acid Sequence , Animals , Cathepsin D/chemistry , Enzyme Stability , Filtration , Hydrogen-Ion Concentration , Hydrolysis , Membranes, Artificial , Solubility , Substrate Specificity
2.
Cell Tissue Res ; 339(3): 571-83, 2010 Mar.
Article in English | MEDLINE | ID: mdl-20127256

ABSTRACT

The tissue distribution and ontogeny of Na(+)/K(+)-ATPase has been examined as an indicator for ion-regulatory epithelia in whole animal sections of embryos and hatchlings of two cephalopod species: the squid Loligo vulgaris and the cuttlefish Sepia officinalis. This is the first report of the immunohistochemical localization of cephalopod Na(+)/K(+)-ATPase with the polyclonal antibody alpha (H-300) raised against the human alpha1-subunit of Na(+)/K(+)-ATPase. Na(+)/K(+)-ATPase immunoreactivity was observed in several tissues (gills, pancreatic appendages, nerves), exclusively located in baso-lateral membranes lining blood sinuses. Furthermore, large single cells in the gill of adult L. vulgaris specimens closely resembled Na(+)/K(+)-ATPase-rich cells described in fish. Immunohistochemical observations indicated that the amount and distribution of Na(+)/K(+)-ATPase in late cuttlefish embryos was similar to that found in juvenile and adult stages. The ion-regulatory epithelia (e.g., gills, excretory organs) of the squid embryos and paralarvae exhibited less differentiation than adults. Na(+)/K(+)-ATPase activities for whole animals were higher in hatchlings of S. officinalis (157.0 +/- 32.4 micromol g (FM) (-1) h(-1)) than in those of L. vulgaris (31.8 +/- 3.3 micromol g (FM) (-1) h(-1)). S. officinalis gills and pancreatic appendages achieved activities of 94.8 +/- 18.5 and 421.8 +/- 102.3 micromol(ATP) g (FM) (-1) h(-1), respectively. High concentrations of Na(+)/K(+)-ATPase in late cephalopod embryos might be important in coping with the challenging abiotic conditions (low pH, high pCO(2)) that these organisms encounter inside their eggs. Our results also suggest a higher sensitivity of squid vs. cuttlefish embryos to environmental acid-base disturbances.


Subject(s)
Cephalopoda/embryology , Embryo, Nonmammalian/metabolism , Epithelium/metabolism , Animals , Antibodies , Blotting, Western , Cephalopoda/anatomy & histology , Cephalopoda/enzymology , Embryo, Nonmammalian/cytology , Embryo, Nonmammalian/enzymology , Epithelium/enzymology , Gills/cytology , Gills/enzymology , Immunohistochemistry , Ions/metabolism , Organ Specificity , Pancreas/cytology , Pancreas/enzymology , Protein Transport , Skin/cytology , Skin/enzymology , Sodium-Potassium-Exchanging ATPase/metabolism
3.
J Mol Histol ; 36(5): 345-53, 2005 Jun.
Article in English | MEDLINE | ID: mdl-16240167

ABSTRACT

Biogenic amines (serotonin and catecholamines), play an important role in the control of the blood flow not only in vertebrates, but also in invertebrates such as cephalopods. In contrast to the well investigated hearts of the a 'modern', coleoid cephalopods, the innervation of the heart of the archaic Nautilus pompilius L. has not been studied in detail. In this study the distribution and effects of biogenic amines in the Nautilus heart were investigated. Serotonin and catecholamines were visualised by the glyxoylic acid induced fluorescence. High performance liquid chromatotography analysis was performed to discriminate between the catecholamines, which showed a high content of noradrenaline in the 4 auricles, the aorta and the ventricle, whereas the ventricle showed a high dopamine content. Adrenaline was found at a very low concentration in the ventricle. Serotonin and dopamine were also immunohistochemically localised to larger nerves and throughout the heart, respectively. In organ bath experiments, the auricles showed little spontaneous activity. After adding serotonin, they displayed rhythmical contractions, which were accelerated dose-dependently by noradrenaline. In summary, these data suggest an important role for biogenic amines in the control of the heart of Nautilus pompilius L., with serotonin possibly stimulating excitatory nerve fibres, whereas noradrenaline is likely to influence the muscle contraction itself.


Subject(s)
Biogenic Amines/metabolism , Cephalopoda/metabolism , Myocardium/metabolism , Animals , Biogenic Amines/physiology , Cephalopoda/enzymology , Chromatography, High Pressure Liquid , Dopamine/metabolism , Female , Fluorescence , Glyoxylates/pharmacology , Heart Ventricles/metabolism , Immunohistochemistry , Male , Monoamine Oxidase/metabolism , Nerve Fibers/metabolism , Pericardium/enzymology , Serotonin/metabolism , Tissue Distribution
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