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Ultraviolet and Visible (UV–Vis) Spectroscopy: Overview01:02

Ultraviolet and Visible (UV–Vis) Spectroscopy: Overview

Ultraviolet–visible (UV–visible or UV–Vis) spectroscopy is an analytical technique that investigates the interaction between matter and UV–Vis light within the electromagnetic spectrum. This method is widely used for its versatility, simplicity, and relatively quick data acquisition, making it valuable for both qualitative and quantitative analysis. When UV–Vis radiation passes through a material,  molecules absorb light depending on the energy required for electronic transitions. As a result...
UV–Vis Spectroscopy of Conjugated Systems01:32

UV–Vis Spectroscopy of Conjugated Systems

Organic compounds with conjugated double bonds show strong absorption features in the UV–visible region of the electromagnetic spectrum attributed to π → π* electronic excitations. Generally, a UV–vis absorption spectrum is recorded as a plot of absorbance vs wavelength. The wavelength of maximum absorbance, which manifests as a peak in the absorption spectrum, is denoted as λmax.
One of the factors influencing λmax is the extent of conjugation in the...
Colors and Magnetism03:02

Colors and Magnetism

Color in Coordination Complexes
When atoms or molecules absorb light at the proper frequency, their electrons are excited to higher-energy orbitals. For many main group atoms and molecules, the absorbed photons are in the ultraviolet range of the electromagnetic spectrum, which cannot be detected by the human eye. For coordination compounds, the energy difference between the d orbitals often allows photons in the visible range to be absorbed and emitted, which is seen as colors by the human eye.
UV–Vis Spectrometers01:14

UV–Vis Spectrometers

The absorbance of UV and visible (UV–visible) radiations is measured using a UV–visible spectrophotometer. Deuterium lamps, which emit UV radiation, and tungsten lamps, which produce radiation in the visible region, are used as light sources in UV–visible spectrophotometers. A monochromator or prism is used for diffraction grating, i.e., to split the incoming radiation into different wavelengths. A system of slits is used to focus the desired wavelength on the sample cell. Samples for...
Urine Studies II: Urine Culture and Sensitivity Test01:26

Urine Studies II: Urine Culture and Sensitivity Test

A urine culture and sensitivity test is a diagnostic procedure used to identify urinary tract bacterial infections and determine the most effective antibiotics for treatment. This test is generally preferred when a patient shows manifestations of a urinary tract infection, such as frequent or painful urination, cloudy or foul-smelling urine, or lower abdominal pain.Purpose of the TestThe primary goals of a urine culture and sensitivity test are to:Determine the specific bacteria causing the...
UV–Vis Spectroscopy: Woodward–Fieser Rules01:29

UV–Vis Spectroscopy: Woodward–Fieser Rules

UV–Visible absorption spectra of conjugated dienes arise from the lowest energy π → π* transitions. The light-absorbing part of the molecule is called the chromophore, and the substituents directly attached to the chromophore are called auxochromes. A strong correlation exists between the absorption maxima, λmax, and the structure of a conjugated π system. The Woodward–Fieser rules predict the value of λmax for a given structure by adding the contributions...

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Related Experiment Video

Updated: May 21, 2026

Hot Biological Catalysis: Isothermal Titration Calorimetry to Characterize Enzymatic Reactions
13:00

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Spectral studies on the interaction between Cu2+ and urease.

Wang Yan-Qing1, Zhang Hong-Mei

  • 1Jiangsu Provincial Key Laboratory of Coastal Wetland Bioresources and Environmental Protection, Institute of Applied Chemistry and Environmental Engineering, Yancheng Teachers University, Yancheng City, Jiangsu Province 224002, People's Republic of China. wyqing76@126.com

Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy
|June 19, 2012
PubMed
Summary

Copper ions (Cu2+) interact with urease, quenching its fluorescence through a spontaneous electrostatic binding process. Spectroscopic analyses reveal changes in urease conformation upon copper binding.

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Area of Science:

  • Biochemistry
  • Biophysics
  • Enzymology

Background:

  • Urease is a crucial enzyme involved in various biological and environmental processes.
  • Understanding the interactions of metal ions with urease is vital for enzyme regulation and applications.
  • Copper ions (Cu2+) are known to affect enzyme activity, but their specific binding mechanisms with urease require detailed investigation.

Purpose of the Study:

  • To elucidate the molecular interactions between copper ions (Cu2+) and urease.
  • To determine the binding parameters and thermodynamic characteristics of Cu2+-urease complex formation.
  • To analyze the conformational changes in urease induced by Cu2+ binding using various spectroscopic techniques.

Main Methods:

  • Fluorescence spectroscopy (intrinsic, synchronous, 3D)
  • UV-Vis absorption spectroscopy
  • Circular Dichroism (CD) spectroscopy

Main Results:

  • Cu2+ effectively quenched the intrinsic fluorescence of urease, indicating a static quenching mechanism.
  • The binding constant (K_A) and binding site number (n) were determined.
  • Thermodynamic parameters revealed a spontaneous molecular interaction driven by electrostatic forces.
  • Spectroscopic data indicated significant alterations in urease conformation upon Cu2+ binding.

Conclusions:

  • The interaction between Cu2+ and urease is a spontaneous process primarily involving electrostatic interactions.
  • Cu2+ binding induces conformational changes in the urease structure.
  • This study provides insights into the mechanism of urease inhibition or modulation by copper ions.