difference absorption spectrum
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1988 ◽  
Vol 255 (3) ◽  
pp. 781-787 ◽  
Author(s):  
T H Liao ◽  
J C Hsieh

The ability of bovine pancreatic DNAase to hydrolyse the synthetic substrate p-nitrophenyl phenylphosphonate (NPPP) is intrinsic and is not due to the contamination of the DNAase preparation by nonspecific phosphodiesterases because the activities of DNA and NPPP hydrolysis are co-eluted from a DEAE-cellulose column with use of the Ca2+-affinity elution method and because the two activities are decreased simultaneously when the purified enzyme is treated with Cu2+/iodoacetate, an active-site-labelling agent for DNAase. NPPP hydrolysis is facilitated by the metal ion-DNAase. At relatively high Na+ concentrations, where the metal ion-DNA interaction is weak, DNA hydrolysis is also facilitated by the metal ion-DNAase. With NPPP as substrate the Michaelis constants are Km 3.7 mM for Mn2+ and Km 49 mM for Mg2+ in 0.2 M-Tris/HCl buffer, pH 7.2. Ca2+ competes with Mn2+, with Ki 64 mM. Free Cu2+ ions non-competitively inhibit DNAase-catalysed DNA or NPPP hydrolysis in the presence of Mn2+ or Mg2+ and the inhibition is not relieved by Ca2+. The affinity of Cu2+ for free DNAase is higher than that for Mn2+-DNAase. Mn2+ is not bound to DNAase via a simple ionic interaction, as Mn2+ remains bound in the presence of relatively high Na+ concentrations and induces a near-u.v. difference absorption spectrum. The kinetics of NPPP hydrolysis catalysed by Mn2+-DNAase are sigmoidal. From the Hill equation, h = 2.0 is obtained, suggesting that more than two NPPP molecules are bound per molecule of DNAase with a certain amount of co-operativity. Because DNAase in solution is a monomer with a single catalytic site, the multiple NPPP molecules on a single protein molecule are probably in one location, resulting in a co-operative interaction that may resemble that in the stacked base-pairs of double-helical DNA.


1943 ◽  
Vol 26 (4) ◽  
pp. 361-367 ◽  
Author(s):  
Alfred F. Bliss

The red pigment in the eyes of the squid, blue crab, and horseshoe crab becomes photosensitive when treated with formalin, and bleaches in the light. The resulting change in density is approximately symmetrical around a maximum at 480 mµ in the blue green. This difference absorption spectrum is in rough agreement with the spectral sensitivity of the cephalopod eye and differs only slightly from the difference absorption spectrum of vertebrate visual purple. The formalin-sensitized pigment is not melanoid. Its bleaching in squid retinas releases large quantities of retinene. It is suggested that the light sensitivity of the normal squid photopigment may be independent of its light stability.


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