acetate buffer works on fumarase activity but tris-maleate buffer does not
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When comparing the structures of acetate buffer and tris-maleate buffer, acetate buffer works on fumarase activity but tris-maleate buffer does not?
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- Discuss the suitability of bromocresol green and thymol blue (2nd change only) for use as indicators in an acetic acid - sodium hydroxide titration. Paragraph в I A + v ...An amino acid mixture consisting of lysine, leucine, and glutamic acid is to be separated by ion-exchange chromatography, using a cationexchange resin at pH 3.5, with the eluting buffer at the same pH. Which of these amino acids will be eluted from the column first? Will any other treatment be needed to elute one of these amino acids from the column?Consider the following pH titration curve of a diprotic acid. What is the approximate values for pka 1 and pka 2? the curve is attached below.
- In ion-exchange chromatography, amino acids are separated on the basis of electro-static interactions and hydrophobic interactions with the resin. The chemical structure of the resin pol-ymer with a negatively charged sulfonic acid group is shown to the right. An elution profile for the aminoacids using this resin is given below. Based on the elution profile above, explain the following:do the calculution for the prepartion of 100mg/ L diclofenac solution, containing 100mg/L of caffeine as an internal standard, in acetonitrile from a stock solution.The pl of alkaline phosphatase is 4.5; the pl of the DEAE cellulose is 10.5. We used a buffer of pH 7.4 to run a DEAE-cellulose as anion exchange column? Explain how did this work?
- An amino acid mixture consisting of lysine,leucine, and glutamic acid is to be separated by ion-exchangechromatography, using a cation-exchange resin at pH 3.5, with theeluting buffer at the same pH. Which of these amino acids will beeluted from the column first? Will any other treatment be neededto elute one of these amino acids from the column?You have been provided with stock solutions of: stock A: 0.06 M sodium pyrophosphate buffer pH 8.5 stock B: 3 M ethanol stock C: 0.015 M NAD+ stock D: milli Q water Determine the volume you will need of each solution to prepare a buffer of with a final volume of 60 mL containing 10 mM sodium pyrophosphate pH 8.5, 100 mM ethanol, 1 mM NAD+. i.e. volume of stock A = _________mL volume of stock B = _________mL volume of stock C = _________mL volume of stock D = _________mL Show your calculations to arrive at your answers.Mixtures of amino acids can be analyzed by first separating the mixture into its components through ion‑exchange chromatography. Amino acids placed on a cation‑exchange resin containing sulfonate (−SO−3)(−SO3−) groups flow down the column at different rates because of two factors that influence their movement: (1) ionic attraction between the sulfonate residues on the column and positively charged functional groups on the amino acids, and (2) aggregation of nonpolar amino acid side chains with the hydrophobic backbone of the polystyrene resin. Note that the ionic attraction is more important than hydrophobicity for this column media. For each pair of amino acids, identify which will be eluted first from a cation‑exchange column using a pH 7.0pH 7.0 buffer.
- What volume of 0.1M NaOH (reagent) needs to be added to increase your 7.5 pH (buffer) by 0.5 pH units. The goal is to further purify MOPs (see image). Protonated form = 6.6 x 10.3^-3 mol/L Deprotonated form = 1.32 x 10^-2 mol/L Show calculations.For the following results of Thermodynamics of Borax Solubility, the volume of Borax solution titrated by HCI is 8.00 mL. Table 1. Volumes of hydrochloric acid required to titrate a saturated borax solution at varying temperatures. The hydrochloric acid was a solution standardized at 0.2912 M. Borax Volume added (mL) Temp. (°C) 8.00 8.00 8.00 8.00 8.00 HCI Volume (mL) 50.5 33.75 40.7 27.02 30.0 17.95 20.2 13.43 10.3 8.55 Using Thermodynamic formula (R= 8.31 J/K•mol) and the above results, (d) AH˚ = (kJ/mol) Type your answer....If a sample of beeswax is found to have an acid number of 15.5 and saponification value of 71.2, the ester value of the sample is: