Biochemistry, The Molecular Basis of Life, 6th Edition
Biochemistry, The Molecular Basis of Life, 6th Edition
6th Edition
ISBN: 9780190259204
Author: Trudy McKee, James R. McKee
Publisher: Oxford University Press
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Chapter 3, Problem 27RQ
Summary Introduction

Interpretation:

The pH of a solution prepared by mixing 300 mL of 0.25 M sodium hydrogen ascorbateand 150 mL of 0.2 M HCl is to be calculated.

Concept introduction:

The pH is the precise measure of the acidity or basicity of a particular solution. It can be calculated as the negative logarithm of H+ (hydrogen ion) concentration.

The Henderson–Hasselbalch expression for a weak acid and its conjugate base is as follows:

pH=pKa+log[A][HA]

Here, pH is the measure of the acidity of the solution, pKa is the negative logarithm of the dissociation constant, [HA] is the concentration of weak acid, and [A] is the concentration of its conjugate base.

The buffer is the combination of weak acid with its conjugate base or a weak base with its conjugate acid. The pH of the buffer solution does not change very much when the strong acid or base added to the buffer solution.

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Fura-2 Fluorescence (Arbitrary Unit) 4500 4000 3500 3000 2500 2000 1500 1000 500 [Ca2+]=2970nM, 25°C [Ca2+] 2970nM, 4°C [Ca2+]=0.9nM, 25°C [Ca2+] = 0.9nM, 4°C 0 260 280 300 340 360 380 400 420 440 Wavelength (nm) ← < The figure on the LHS shows the excitation spectra of Fura-2 (Em = 510 nm) in 2 solutions with two different Ca2+ ion concentration as indicated. Except for temperature, the setting for excitation & signal acquisition was identical.< ப a) The unit in Y-axis is arbitrary (unspecified). Why? < < b) Compare & contrast the excitation wavelength of the Isosbestic Point of Fura-2 at 25 °C & 4 °C. Give a possible reason for the discrepancy. < c) The fluorescence intensity at 25 °C & 4 °C are different. Explain why with the concept of electronic configuration. <

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