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The metabolism of adenosine nucleotides in thoracic muscle mitochondria from the American cockroachMills, Richard Randolph January 1964 (has links)
Myokinase and three inorganic pyrophosphatases with pH optima of 6.4, 7.2 and 8.4 have been isolated and purified from the thoracic muscle mitochondria of the American cockroach.
Myokinase was purified over 100-fold by heat and acid treatment, ammonium sulfate fractionation and column chromatography on G-75 sephadex. Some properties of the enzyme were determined. These include: a pH optimum of 5.8, an optimum Mg concentration of 3 x 10⁻³ M, a substrate specificity for ADP, and an equilibrium constant of 0.44. In addition, Km and Ki values were determined for each adenosine nucleotide, inhibition studies were conducted, and the enzyme was found to have the greatest stability against heat denaturation at a neutral pH. From the results obtained here it appears that the enzyme apyrase is not responsible for the rapid dephosphorylation of ATP. In addition, this study indicates that a specific triphosphatase coupled with myokinase produces the products AMP and P<sub>i</sub> which are found when crude homogenates are used as the enzyme.
The three inorganic pyrophosphatases were purified by sonication, ultracentrifugation, ammonium sulfate fractionation, and column chromatography on G-75 sephadex, DEAE cellulose, and CM cellulose. The three enzymes were found to have distinct pH optima: one acid, one neutral and one alkaline. The enzyme activated at a neutral pH needed only one-half as much Mg as substrate. The optimum ratio for the other two enzymes was one to one. Substrate specificity studies indicated that the enzymes may be important in the breakdown of polyphosphates and GTP. No other high energy phosphate bonds were acted on. The physiological significance remains obscure although data from this study indicate that an important function of the enzymes may be to remove undesirable pyrophosphate from the mitochondria. / Ph. D.
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An investigation into the physiology of urate pellet excretion by Parcoblatta fulvescens (Saussure and Zehntner) (Dictyoptera: Blattellidae)Lembke, Hannah January 1985 (has links)
Physiological parameters involved in formed urate pellet excretion by the wood cockroach, <i>Parcoblatta fulvescens</i> were investigated.
Uric acid excretion by last instar juvenile <i>P. fulvescens</i> was studied first. Food consumption, urate and non-urate pellet excretion patterns show a skewed distribution with peak feeding occurring on day six and peak voiding of both pellet types on day seven of a 17.0 ± 2.0 (SD) day ecdysial cycle. The amount of urates excreted is determined by the level of dietary protein (p<0.0001) and is linearly related to protein consumption.
Selective feeding on protein, carbohydrate and cellulose diets by reproductive female <i>P. fulvescens</i> was investigated. Separate consumption patterns exist for each diet. These females did not excrete uric acid.
Urate pellet consumption by reproductive female <i>P. fulvescens</i> was examined in relation to dietary protein and carbohydrate. Urate pellet consumption increases with decreasing protein and increasing carbohydrate levels. Females that consume urate pellets do not excrete uric acid. These results suggest that urate-containing pellets serve to transfer nitrogen reserves among individuals.
Urate spherules were enzymatically and histochemically identified in the middle and proximal regions of the Malpighian tubules of <i>P. fulvescens</i>, <i>Shawella couloniana</i> and <i>Symploce hospes</i>. These spherules are discharged into the hindgut in sufficient quantities to obscure the presence of food residues.
The significance of formed urate pellet excretion is discussed in relation to the nitrogen economy of <i>Parcoblatta fulvescens</i>. / Master of Science / incomplete_metadata
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