Martinoia E., Locher R., Vogt E.
Institute of Plant Sciences, Swiss Federal Institute of Technology, Zurich Sonneggstrasse 5, ETH-Z, CH-8092 Zurich, Switzerland (E.M., E.V.).
Plant Physiol. 1993 May;102(1):101-105. doi: 10.1104/pp.102.1.101.
Phosphatases in cytosolic fractions, vacuoles, and vacuolar membranes from barley (Hordeum vulgare L.) leaves were found to dephosphorylate inositol 1,4,5-trisphosphate (IP3). 1,4-inositol bisphosphate (1,4-IP2) is the main product of IP3 dephosphorylation by the cytosolic fraction. The activity was strictly Mg2+ dependent. In contrast, IP3 dephosphorylation activity of both the soluble vacuolar and the tonoplast fractions was inhibited up to 50% by Mg2+. When vacuolar membranes were incubated with IP3, 1,4-IP2 was produced only under neutral and slightly alkaline conditions. Under acidic conditions, however, dephosphorylation yielded putative 4,5-inositol bisphosphate. Li+ (20 mM) and Ca2+ (100 [mu]M) strongly inhibited activity in the soluble vacuolar fraction but had only a slight effect on the activities of the cytosolic and tonoplast fractions.
在大麦(Hordeum vulgare L.)叶片的胞质组分、液泡和液泡膜中发现的磷酸酶能够使肌醇1,4,5-三磷酸(IP3)去磷酸化。1,4-肌醇二磷酸(1,4-IP2)是胞质组分使IP3去磷酸化的主要产物。该活性严格依赖Mg2+。相反,可溶性液泡组分和液泡膜组分的IP3去磷酸化活性被Mg2+抑制高达50%。当液泡膜与IP3一起温育时,仅在中性和略碱性条件下产生1,4-IP2。然而,在酸性条件下,去磷酸化产生假定的4,5-肌醇二磷酸。Li+(20 mM)和Ca2+(100 μM)强烈抑制可溶性液泡组分中的活性,但对胞质组分和液泡膜组分的活性仅有轻微影响。