Toluene permeabilization differentially affects F- and P-type ATPase activities present in the plasma membrane of Streptococcus mutans

Streptococcus mutans membrane-bound P- and F-type ATPases are responsible for H+ extrusion from the cytoplasm thus keeping intracellular pH appropriate for cell metabolism. Toluene-permeabilized bacterial cells have long been used to study total membrane-bound ATPase activity, and to compare the properties of ATPase in situ with those in membrane-rich fractions. The aim of the present research was to determine if toluene permeabilization can significantly modify the activity of membrane-bound ATPase of both F-type and P-type. ATPase activity was assayed discontinuously by measuring phosphate release from ATP as substrate. Treatment of S. mutans membrane fractions with toluene reduced total ATPase activity by approximately 80% and did not allow differentiation between F- and P-type ATPase activities by use of the standard inhibitors vanadate (3 µM) and oligomycin (4 µg/mL). Transmission electron microscopy shows that, after S. mutans cells permeabilization with toluene, bacterial cell wall and plasma membrane are severely injured, causing cytoplasmic leakage. As a consequence, loss of cell viability and disruption of H+ extrusion were observed. These data suggest that treatment of S. mutans with toluene is an efficient method for cell disruption, but care should be taken in the interpretation of ATPase activity when toluene-permeabilized cells are used, because results may not reflect the real P- and F-type ATPase activities present in intact cell membranes. The mild conditions used for the preparation of membrane fractions may be more suitable to study specific ATPase activity in the presence of biological agents, since this method preserves ATPase selectivity for standard inhibitors.UNIUBECNPqCoordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES

Quantitative atomic force microscopy provides new insight into matrix vesicle mineralization

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A carbohydrate pulse experiment to demonstrate the sugar metabolization by S. mutans

Streptococcus mutans is a fast growing organism, of low cost and easily prepared culture medium. It has been  related  primarily to  an  elevated risk  of dental cavity development  in the host due  to the  acid-induced tooth demineralization. To prevent this disease, addition of fluoride can be required, promoting the mouth  hygiene. The  main  objective  of  this  experiment  is  to  show  the  influence  of  the  carbon  source  and fluoride on the acidogenic capacity of S.  mutans. The strain was cultivated in microaerophilia, at 37ºC for 12  hours  in  complete  medium  (stationary  phase).  The  cells  were  harvested  by  centrifugation  at  room temperature,  washed  with  saline  solution  and  suspended  in  the  same  solution.  The  absorbance  was adjusted  to  1  and  the  pH  to  7.3  using  0,1  mol/L  KOH  solution.  To  10  mL  of  the  cell  suspension,  distinct carbohydrates  (glucose,  xilose,  sucrose,  fructose  or  maltose)  were  added,  enough  to  establish  a  50 mMol/L final concentration. Fluoride was added (1 mmol/L final concentration) and the pH was monitored during  2 hours. In this  incubation  period,  the  suspension  was  kept  at  room  temperature  with  slow  stirring and  the  pH  was  monitored  each  7  minutes.  In  the  20  initial  minutes  of  incubation  with  glucose,  fructose, maltose  and  sucrose,  an  intense  and  very  similar  pH  decrease  (2.5  units)  can  be  observed.  This acidification reflects both the sugar uptake and anaerobic metabolization. After this initial acid liberation, a phase of slow pH decrease is observed, continuing up to 120 minutes of incubation. In presence of xilose, the  acidification  is  less  intense  and  reaches  a  similar  value  to  that  of  the  control  without  carbohydrate addition (decreasing  1.4 units  of pH). The  initial  acidification  in the presence of xilose  may  occur  due  to the mechanism of sugar uptake by this organism, which involves the antiport with H+. In media without the addition  of  carbohydrate,  the  acidification  may  be  due  to  the  metabolization  of  intracellular  reserves  of sugars. Fluoride affects negatively the acidogenic capacity of S. mutans for all metabolized sugars

The effect of cholesterol on the reconstitution of alkaline phosphatase into liposomes

Tissue-nonspecific alkaline phosphatase (TNAP), present on the surface of chondrocyte- and osteoblast-derived matrix vesicles (MVs), plays key enzymatic functions during endochondral ossification. Many studies have shown that MVs are enriched in TNAP and also in cholesterol compared to the plasma membrane. Here we have studied the influence of cholesterol on the reconstitution of TNAP into dipalmitoylphosphatidylcholine (DPPC)-liposomes, monitoring the changes in lipid critical transition temperature (T(c)) and enthalpy variation (Delta H) using differential scanning calorimetry (DSC). DPPC-liposomes revealed a T(c) of 41.5 degrees C and Delta H of 7.63 Kcal mol(-1). The gradual increase in cholesterol concentration decrease Delta H values, reaching a Delta H of 0.87 Kcal mol(-1) for DPPC: cholesterol system with 36 mol% of cholesterol. An increase in T(c), up to 47 degrees C for the DPPC:cholesterol liposomes (36 mol% of Chol), resulted from the increase in the area per molecule in the gel phase. TNAP (0.02 mg/mL) reconstitution was done with protein:lipid 1:10,000 (molar ratio), resulting in 85% of the added enzyme being incorporated. The presence of cholesterol reduced the incorporation of TNAP to 42% of the added enzyme when a lipid composition of 36 mol% of Chol was used. Furthermore, the presence of TNAP in proteoliposomes resulted in a reduction in Delta H. The gradual proportional increase of cholesterol in liposomes results in broadening of the phase transition peak and eventually eliminates the cooperative gel-to-liquid-crystalline phase transition of phospholipids bilayers. Thus, the formation of microdomains may facilitate the clustering of enzymes and transporters known to be functional in MVs during endochondral ossification. (C) 2010 Elsevier B.V. All rights reserved.FAPESPCAPESCNP