Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: EC:2.3.1.177 (BIS)
 957 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The effect of N-TRIS(hydroxymethyl)methyl-2-aminoetane sulfonic acid (TES); N,N BIS (2 hydroxvethyl)-2 aminoethane sulfonic acid (BES), N-2(hydroxyethyl)piperazine-N-2-ethane sulfonic acid (HEPES), morpholinopropane sulfonic acid (MOPS), and piperazine-N-N-BIS(2-ethane sulfonic acid (PIPES) solutions on dialyzed semen was studied. Each was titrated to pH 7.0 with TRIS-(hydroxymethyl)-amino methane (TRIS) solution and the osmotic pressure was adjusted to between 320 to 325 mOsm/kg. The new solutions were identified as TEST, BEST, HEPEST, MOPST and PIPEST, respectively. The solutions were used 1) alone, 2) in a composite with equal parts (V/V) of each solution and 3) in a 1:1 (V/V) combination with isosmotic trisodium citrate solution. Later, TRIS and sodium hydroxide (NaOH) were compared as titration bases for piperazine-N-N-BIS (2-ethane sulfonic acid) (PIPES) and N-Tris(hydroxymethyl)methyl-2-aminoethane sulfonic acid (TES). Ejaculates were diluted 1:10 (V/V) in extenders containing buffer, 20% egg yolk and 5% glycerol (V/V). The samples were dialyzed (1:50) during cooling for a period of 2 h. Each sample was dialyzed against the same buffer system containing 5% glycerol without egg yolk and later it was frozen in pellets. The treatments were evaluated by observation of sperm motility in fresh and thawed semen samples. The latter were also analyzed by electronic count of cells that passed through the Sephadex column. Sperm survival was higher in PIPEST (PIPES titrated with TRIS) or the composite buffer, and the inclusion of 50% sodium citrate (Na citrate) improved significantly (P<0.05) sperm motility in fresh and frozen-thawed semen samples. There was no difference (P>0.05) between the titration bases. In the second experiment, sperm survival was superior in extenders containing PIPEST (P<0.05) than in those containing TEST independently of the inclusion of Na citrate.
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PMID:Development of a buffer system for dialysis of bovine spermatozoa before freezing. I. Effect of zwitterion buffers. 1672 19

Three experiments were conducted to study the effect of inorganic and organic acids on survival of dialyzed bovine spermatozoa. Ejaculates were pooled, extended (1:10), dialyzed (1:50) for 2 h during cooling, and 1 h later they were frozen in pellets and stored in liquid nitrogen. The pellets were thawed in aluminum block depressions (preheated at 45 degrees C) and transferred to a test tube at room temperature as the last ice melted. Sperm motility was recorded in all samples before freezing and after thawing. The number of spermatozoa that passed through the Sephadex column was analyzed in all the postthaw samples. No statistical difference (P>0.05) was found between the use of potassium (KOH) or sodium hydroxide (NaOH) as titration bases. However, solutions containing calcium (Ca++) or magnesium (Mg++) provided significantly less (P<0.05) protection to the cells during freezing and thawing. No significant difference (P>0.05) was found in sperm survival of the postthaw samples when Ca++ or Mg++ were present. Inorganic salts of phosphates, carbonates or chloride provided significantly less protection to the cells than the control extenders with Na citrate (P<0.05). Results of the second experiment indicated that citrate, tartrate and oxalate salts provided superior (P<0.05) protection to the cells than salts of succinate, acetate or formate. It was concluded that an appropriate solution for use as a dialysate of extended bovine spermatozoa may be formulated as 30% (V/V) isosmotic Na salt of Piperazine-N-N-BIS (2-ethane sulfonic acid) (PIPES) plus 30% (V/V) isosmotic glucose plus 5% (V/V) glycerol plus 35% (V/V) of isosmotic solutions of Na or K citrate or tartrate, or a (1:1) combination of them.
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PMID:Development of a buffer system for dialysis of bovine spermatozoa before freezing. III. Effect of different inorganic and organic salts on fresh and frozen-thawed semen. 1672 21

An excess or lack of fluoride in drinking water is harmful to human health. Desirable and permissible standards of fluoride in drinking water are 1.0 and 1.5 mg/L, respectively, as per Indian drinking water quality standards i.e., BIS 10500, 1991. In this paper, the performance of an electro-coagulation defluoridation batch process with aluminium electrodes was investigated. Different operational conditions such as fluoride concentration in water, pH and current density were varied and performance of the process was examined. Influence of operational conditions on (i) electrode polarization phenomena, (ii) pH evolution during electrolysis and (iii) the amount of aluminium released (coagulant) was investigated. Removal by electrodes is primarily responsible for the high defluoridation efficiency and the adsorption by hydroxide aluminium floc provides secondary effect. Experimental data obtained at optimum conditions that favored simultaneous mixing and flotation confirmed that concentrations lower than 1 mg/L could be achieved when initial concentrations were between 2 and 20 mg/L. pH value was found to be an important parameter that affected fluoride removal significantly. The optimal initial pH range is between 6 and 7 at which effective defluoridation and removal efficiencies over 98% were achieved. Furthermore, experimental results prominently displayed that an increase in current density substantially reduces the treatment duration, but with increased residual aluminium level. The paper focuses on pilot scale defluoridation process optimization along with aluminium leaching and experimental results were compared with a full-scale plant having capacity of 600 liter per batch.
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PMID:Lab scale study on electrocoagulation defluoridation process optimization along with aluminium leaching in the process and comparison with full scale plant operation. 2204