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PMID: 4392239 Published · ppublish English Journal Article

The chemistry of flavins and flavoproteins: aerobic photochemistry.

The Biochemical journal ·Vol. 116 ·No. 4 ·1970-02-00 ·Pages 733-43

Penzer GR

Abstract

1. When a mixture of FMN and a reducing substrate (e.g. unprotonated amine) is illuminated oxygen is consumed. 2. The rate of oxygen uptake increases as oxygen concentration falls with some substrates (type I reaction), but with other substrates (typically aromatic compounds) the rate falls as the oxygen concentration falls (type II reaction). 3. The kinetics of type I reactions with EDTA, dl-alpha-phenylglycine and diethanolamine are all consistent with a mechanism in which the rate-determining step, hydrogen abstraction by the FMN triplet, is followed by rapid reoxidation of reduced FMN by oxygen. The reaction is faster at low oxygen concentrations because oxygen quenches the triplet. 4. The sensitivity of reaction rates to substituents in dl-alpha-phenylglycine can be described by a Hammett rho value of -0.6. 5. Individual rate constants for quenching and reaction of the FMN triplet with substrate were calculated (2.4x10(8) and 2.1x10(7)m(-1)s(-1) respectively for EDTA) on the assumption that oxygen quenches the triplet in a diffusion-controlled reaction. 6. The pH-dependences of oxygen uptake rates with six natural amino acids as substrates were measured. 7. Photoinactivations of l-glutamate dehydrogenase and d-amino acid oxidase by FMN were demonstrated.

MeSH Terms
Amino Alcohols Animals Cattle D-Amino-Acid Oxidase/antagonists & inhibitors Diffusion Edetic Acid Flavin Mononucleotide/pharmacology,radiation effects Glutamate Dehydrogenase/antagonists & inhibitors Glycine/metabolism Hydrogen-Ion Concentration Kinetics Light Oxygen Consumption Radiation Effects
Chemicals
Amino Alcohols Flavin Mononucleotide Edetic Acid Glutamate Dehydrogenase D-Amino-Acid Oxidase Glycine
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Penzer G R
References (10)
10 references, click to expand
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  7. Catalysis of oxidation of nitrogen compounds by flavin coenzymes in the presence of light.
    J Biol Chem. 1959 May;234(5):1297-302 PMID: 13654365
  8. Structure and function of D-amino acid oxidase. I. Further purification of hog kidney D-amino acid oxidase and its hydrodynamic and optical rotatory properties.
    J Biochem. 1967 May;61(5):580-97 PMID: 4383484
  9. A flash-photolysis investigation of flavin photosensitization of purine nucleotides.
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Article Info
Journal
The Biochemical journal
Abbr.
Biochem J
ISSN
0264-6021
Published
1970-02-00
Pages
733-43
Language
English
Region
England
NLM ID
2984726R
PMCID
PMC1185419
Subset
IM
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