Literature DB >> 4386790

Purification and properties of mutant and wild-type diaphorases from Diplococcus pneumoniae.

A S Kreger, R H Olsen.   

Abstract

Optochin-resistant mutant and wild-type diaphorases were purified approximately 300-fold by a combination of batch adsorption and column chromatography with diethylaminoethyl cellulose, and were characterized with regard to their pH optima, sensitivity to optochin inhibition and heat inactivation, Michaelis constants with flavine mononucleotide (FMN) and reduced nicotinamide adenine dinucleotide (NADH), and inhibition constants with optochin hydrochloride. The pH optima of the purified diaphorases were similar, but the purified diaphorases from the optochin-resistant strains were approximately four to five times more resistant to heat inactivation at 45 C than was the wild-type diaphorase. Purified diaphorase preparations from the optochin-resistant pneumococci had greater activities per milligram of protein and were more resistant to optochin inhibition than the preparation from the optochin-sensitive pneumococcus. Michaelis constants for FMN and NADH were similar; however, the inhibition constants of the optochin-resistant diaphorases were four to eight times greater than that of the optochin-sensitive diaphorase. Optochin hydrochloride produced a noncompetitive type of inhibition with FMN as substrate but a competitive type of inhibition with NADH as substrate. Optochin hydrochloride produced an approximately 10-fold increase in the Michaelis constant for NADH. The concentration of drug required to produce this effect was, however, greater with the mutant diaphorases than with the wild-type diaphorase. Optochin hydrochloride quenched the fluorescence of riboflavine. This phenomenon did not appear to be related to the diaphorase-inhibitory activity of the drug, however, since the pH requirements of the two reactions were different. Quenching of riboflavine fluorescence by optochin hydrochloride increased with a rise in pH, whereas inhibition of diaphorase activity by optochin hydrochloride was greater at pH 6.8 than at pH 7.6.

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Year:  1968        PMID: 4386790      PMCID: PMC252414          DOI: 10.1128/jb.96.4.1029-1036.1968

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  10 in total

1.  Role of vitamin K in electron transport.

Authors:  W D WOISLAIT
Journal:  Fed Proc       Date:  1961-12

2.  A microcolorimetric method for the determination of inorganic phosphorus.

Authors:  H H TAUSSKY; E SHORR
Journal:  J Biol Chem       Date:  1953-06       Impact factor: 5.157

3.  Enzymatic Studies on the Mechanism of the Resistance of Pneumococcus to Drugs: II. The Inhibition of Dehydrogenase Activities by Drugs; Antagonistic Effects of Riboflavin to Inhibitions.

Authors:  M G Sevag; J S Gots
Journal:  J Bacteriol       Date:  1948-12       Impact factor: 3.490

4.  Enzymatic Studies on the Mechanism of the Resistance of Pneumococcus to Drugs: III. Experimental Results Indicating Alteration in Enzyme Proteins Associated with the Development of Resistance to Drugs.

Authors:  M G Sevag; J S Gots
Journal:  J Bacteriol       Date:  1948-12       Impact factor: 3.490

5.  Protein measurement with the Folin phenol reagent.

Authors:  O H LOWRY; N J ROSEBROUGH; A L FARR; R J RANDALL
Journal:  J Biol Chem       Date:  1951-11       Impact factor: 5.157

6.  The stabilization of D-amino acid oxidase by flavin-adenine dinucleotide, substrates and competitive inhibitors.

Authors:  K BURTON
Journal:  Biochem J       Date:  1951-04       Impact factor: 3.857

7.  Differentiating properties of the dihydrofolate reductases of amethopterin-resistant Streptococcus faecalis/Ak and the sensitive parent strain.

Authors:  A M Albrecht; J L Palmer; D J Hutchison
Journal:  J Biol Chem       Date:  1966-03-10       Impact factor: 5.157

8.  The biochemical mechanisms of resistance by streptococci to the antibiotics D-cycloserine and O-carbamyl-D-serine.

Authors:  R H Reitz; H D Slade; F C Neuhaus
Journal:  Biochemistry       Date:  1967-08       Impact factor: 3.162

9.  Altered diaphorase activity in optochin-resistant pneumococci.

Authors:  A S Kreger; R H Olsen; M B Talmadge
Journal:  J Bacteriol       Date:  1968-10       Impact factor: 3.490

10.  Diaphorases from Aerobacter aerogenes.

Authors:  C Bernofsky; R C Mills
Journal:  J Bacteriol       Date:  1966-11       Impact factor: 3.490

  10 in total
  2 in total

1.  Microarray analysis of pneumococcal gene expression during invasive disease.

Authors:  Carlos J Orihuela; Jana N Radin; Jack E Sublett; Geli Gao; Deepak Kaushal; Elaine I Tuomanen
Journal:  Infect Immun       Date:  2004-10       Impact factor: 3.441

2.  Altered diaphorase activity in optochin-resistant pneumococci.

Authors:  A S Kreger; R H Olsen; M B Talmadge
Journal:  J Bacteriol       Date:  1968-10       Impact factor: 3.490

  2 in total

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