scholarly journals A double-beam rapid-scanning stopped-flow spectrophotometer

1975 ◽  
Vol 149 (1) ◽  
pp. 221-231 ◽  
Author(s):  
M R Holloway ◽  
H A White

A double-beam rapid-wavelength-scanning stopped-flow spectrophotometer system based on the Norcon model 501 spectrometer was construced, which enables u.v.-or visible absorbance spectra to be recorded at the rate of 800/s after the rapid mixing (within 3ms) of two reactant solutions. Each spectrum spans about 200nm in 1ms. It is possible to record difference spectra during reactions with half-lives less than 10ms involving absorbance changes of less than 0.1 absorbance unit. Analogue circuitry is used to produce spectra of absorbance against wavelength. Up to 32 such spectra can be recorded at pre-selected times during a reaction and stored in an 8K×8-bit-word hard-wired data-capture system to be subsequently displaned individually or simultaneously. Time-courses at different wavelengths can also be displayed. By averaging up to 216 spectra it is possible to record spectra under conditions of low signal-to-noise ratios. Examples are given of the application of the system in recording: (a) the spectrum of NADH (2mol/mol of enzyme) produced in the pre-steady-state phase of the horse liver alcohol dehydrogenase-catalysed oxidation of ethanol; (b) the spectrum of NADH (4mol/mol of enzyme) produced in a single turnover in the glyceraldehyde 3-phosphate dehydrogenase reaction; (c) spectral changes during the reaction of aquocobalamin and dithionite; (d) spectral changes during thereaction ofcyanmethaemoglobin and dithionite; (e) the release of thionitrobenzoate and production of NADH when thiol-modified glyceraldehyde 3-phosphate dehydrogenase is mixed with dithiothreitol and substrates.

1973 ◽  
Vol 28 (5-6) ◽  
pp. 247-254 ◽  
Author(s):  
Dietmar Scherr ◽  
Reinhard Jeck ◽  
Jürgen Berghäuser ◽  
Christoph Woenckhaus

The spectral properties of binary complexes of NAD-analogues and fragments therefrom with I.DH from pig heart or ADH from liver and yeast have been investigated. The NADH-analogues were modified by replacing adenine through benzimidazole, benzene or dihydronicotinamide. Additionally adenosine diphosphate ribose, dihydronicotinamide and dihydronicotinamide- ribose pyrophosphate-5"-ribose have been studied. It has been shown by means of difference spectra that complexes between ADH from horse liver and analogues cause spectral changes in the region of aromatic absorption at 280 nm even when adenine is absent in the analogues. Spectral changes in the other enzymes mentioned are probably due to changes of the n-π* absorption of the adenine ring. The spectral changes upon complexing indicate hydrophobic interaction of the adenine with the enzyme protein. Fluorescence spectra vary in the intensity of the energy transfer band as well as in coenzyme emission depending on variation of the coenzym analogue. Changing of complex formation between protein and analogues at different pH-values are investigated. ADH from yeast, especially, shows a pK around 6 which suggests interaction with histidine imidazole.


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