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Characteristics of phosphatidylinositol synthase activity from Tetrahymena
Author(s) -
LANSLEY TANYA A.,
MOYE BRANDY R.,
CHAN EDMOND R.,
RYALS PHILLIP E.
Publication year - 2005
Publication title -
journal of eukaryotic microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.067
H-Index - 77
eISSN - 1550-7408
pISSN - 1066-5234
DOI - 10.1111/j.1550-7408.2005.05202003_1_45.x
Subject(s) - phosphatidylinositol , tetrahymena , substrate (aquarium) , incubation , enzyme , atp synthase , inositol , biology , biochemistry , phospholipase c , receptor , signal transduction , ecology
Properties of phosphatidylinositol synthase (PtdIns‐synthase) from the ciliate Tetrahymena were investigated using microsomal fractions enriched for the enzyme. Optimum conditions for PtdIns‐synthase activity as assayed in a Triton X‐100/CDP‐DAG mixed micelle system with [ 3 H] myo ‐Ins as co‐substrate were a pH of 8.0 using 50 mM Tris‐HCl buffer and a temperature of 30°C. Incubation of PtdIns‐synthase at pre‐selected temperatures prior to assay at 30°C showed that the enzyme was stable for at least 20 min at 40°C. A sharp decline in activity was seen after incubation at 50°C for 20 min. Activity was stimulated by 2 mM Mg 2+ , and stimulated to a slightly lesser degree by 1 mM Mn 2+ ; however, these two ions in combination were synergistic. Other metal cations (Ca, Co, Cu, Fe, Mo, Zn, and Li) at a concentration of 2 mM had no appreciable effect on activity. Under optimum assay conditions, Tetrahymena PtdIns‐synthase activity was linear over at least 20 min and was linear with increasing concentrations of the enzyme. The enzyme was capable of utilizing both [ 3 H] scyllo ‐and [ 3 H] (1D) chiro ‐Ins as substrate to form phosphatidyl‐[ 3 H] scyllo ‐and phosphatidyl‐[ 3 H](1D) chiro ‐inositol, respectively, with (1D)chiro‐inositol being the least preferred substrate. The in vitro synthesized myo ‐and scyllo ‐inositol‐containing phosphoinositides were susceptible to hydrolysis by Bacillus cereus phosphatidylinositol‐specific phospholipase C, but the (1D) chiro ‐inositol phosphoinositide was resistant. We hypothesize that putative DAG and scyllo ‐IP 3 second messengers produced by the cleavage of polyphospho‐scyllo‐inositides may function in novel transmembrane signaling cascades.