TY - JOUR
T1 - Biochemical characterization of a phosphatidylinositol 4,5-bisphosphate-specific phospholipase C activity in gills and digestive gland of the marine mussel Mytilus galloprovincialis lam
AU - Panfoli, I.
AU - Morelli, A.
AU - Viarengo, A.
AU - Orunesu, M.
PY - 1993/5
Y1 - 1993/5
N2 - 1. 1. Polyphosphoinositide-specific phosphodiesterase (phospholipase C, PLC) activity against phosphatidylinositol 4,5-bisphosphate, present in gill and digestive gland homogenates of mussel (Mytilus galloprovincialis Lam.), has been biochemically characterized. 2. 2. The enzyme was strictly modulated by free calcium ion concentration in both tissues and maximally activated at 10-5 M Ca2+ (19 ± 4 and 11 ± 2 nmol phosphatidylinositol 4,5-bisphosphate hydrolysed/min/mg of protein for gill and digestive gland PLC, respectively, at 19°C). Optimum pH at 10-5 M Ca2+ was around 7.0 in both cases. The Ca2+-stimulated PLC activity showed high specificity for PIP2; the KMa for PIP2 were 150 and 170 μM for the gills and digestive gland, respectively. 3. 3. Good substrate dispersion was obtained in the presence of sodium deoxycholate; the concentration routinely used in the assay (0.08%) produced a 9-fold activation of both gill and digestive gland PLC, consistent with previous reports. 4. 4. The possible biochemical and physiological role of the enzyme in mussel tissues is discussed.
AB - 1. 1. Polyphosphoinositide-specific phosphodiesterase (phospholipase C, PLC) activity against phosphatidylinositol 4,5-bisphosphate, present in gill and digestive gland homogenates of mussel (Mytilus galloprovincialis Lam.), has been biochemically characterized. 2. 2. The enzyme was strictly modulated by free calcium ion concentration in both tissues and maximally activated at 10-5 M Ca2+ (19 ± 4 and 11 ± 2 nmol phosphatidylinositol 4,5-bisphosphate hydrolysed/min/mg of protein for gill and digestive gland PLC, respectively, at 19°C). Optimum pH at 10-5 M Ca2+ was around 7.0 in both cases. The Ca2+-stimulated PLC activity showed high specificity for PIP2; the KMa for PIP2 were 150 and 170 μM for the gills and digestive gland, respectively. 3. 3. Good substrate dispersion was obtained in the presence of sodium deoxycholate; the concentration routinely used in the assay (0.08%) produced a 9-fold activation of both gill and digestive gland PLC, consistent with previous reports. 4. 4. The possible biochemical and physiological role of the enzyme in mussel tissues is discussed.
UR - https://www.scopus.com/pages/publications/0027190616
U2 - 10.1016/0305-0491(93)90180-D
DO - 10.1016/0305-0491(93)90180-D
M3 - Article
SN - 0305-0491
VL - 105
SP - 139
EP - 145
JO - Comparative Biochemistry and Physiology - B Biochemistry and Molecular Biology
JF - Comparative Biochemistry and Physiology - B Biochemistry and Molecular Biology
IS - 1
ER -