Studies on reactions of oxidizing sulfur–sulfur three-electron-bond complexes and reducing α-amino radicals derived from OH reaction with methionine in aqueous solution

The technique of pulse radiolysis with spectrophotometric detection has been used to investigate the possibility of electron transfer reactions between oxidizing sulfur–sulfur three-electron-bond complexes (Met 2/S∴S +), or reducing α-amino radicals (CH 3SCH 2CH 2CH ⋅NH 2) derived from reaction of m...

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Published inBiochimica et biophysica acta Vol. 1525; no. 1; pp. 89 - 96
Main Authors Lu, Changyuan, Yao, Side, Lin, Nianyun
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 16.02.2001
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ISSN0304-4165
0006-3002
1872-8006
DOI10.1016/S0304-4165(00)00174-4

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Abstract The technique of pulse radiolysis with spectrophotometric detection has been used to investigate the possibility of electron transfer reactions between oxidizing sulfur–sulfur three-electron-bond complexes (Met 2/S∴S +), or reducing α-amino radicals (CH 3SCH 2CH 2CH ⋅NH 2) derived from reaction of methionine with OH radicals and hydroxycinnamic acid (HCA) derivatives, riboflavin (RF) or flavin adenine dinucleotide (FAD), respectively. The HCA derivatives, such as caffeic acid, ferulic acid, sinapic acid and chlorogenic acid, widely distributed phenolic acids in fruit and vegetables, have been identified as good antioxidants previously can rapidly and efficiently repair oxidizing three-electron-bond complexes via electron transfer. RF and FAD can oxidize reducing α-amino radicals derived from methionine. The electron transfer rate constants ∼10 9 dm 3 mol −1 s −1 were determined by following the build-up kinetics of species produced.
AbstractList The technique of pulse radiolysis with spectrophotometric detection has been used to investigate the possibility of electron transfer reactions between oxidizing sulfur–sulfur three-electron-bond complexes (Met 2/S∴S +), or reducing α-amino radicals (CH 3SCH 2CH 2CH ⋅NH 2) derived from reaction of methionine with OH radicals and hydroxycinnamic acid (HCA) derivatives, riboflavin (RF) or flavin adenine dinucleotide (FAD), respectively. The HCA derivatives, such as caffeic acid, ferulic acid, sinapic acid and chlorogenic acid, widely distributed phenolic acids in fruit and vegetables, have been identified as good antioxidants previously can rapidly and efficiently repair oxidizing three-electron-bond complexes via electron transfer. RF and FAD can oxidize reducing α-amino radicals derived from methionine. The electron transfer rate constants ∼10 9 dm 3 mol −1 s −1 were determined by following the build-up kinetics of species produced.
The technique of pulse radiolysis with spectrophotometric detection has been used to investigate the possibility of electron transfer reactions between oxidizing sulfur-sulfur three-electron-bond complexes (Met2/S thereforeS+), or reducing alpha-amino radicals (CH3SCH2CH2CH.NH2) derived from reaction of methionine with OH radicals and hydroxycinnamic acid (HCA) derivatives, riboflavin (RF) or flavin adenine dinucleotide (FAD), respectively. The HCA derivatives, such as caffeic acid, ferulic acid, sinapic acid and chlorogenic acid, widely distributed phenolic acids in fruit and vegetables, have been identified as good antioxidants previously can rapidly and efficiently repair oxidizing three-electron-bond complexes via electron transfer. RF and FAD can oxidize reducing alpha-amino radicals derived from methionine. The electron transfer rate constants approximately 10(9) dm3 x mol(-1)x s(-1) were determined by following the build-up kinetics of species produced.The technique of pulse radiolysis with spectrophotometric detection has been used to investigate the possibility of electron transfer reactions between oxidizing sulfur-sulfur three-electron-bond complexes (Met2/S thereforeS+), or reducing alpha-amino radicals (CH3SCH2CH2CH.NH2) derived from reaction of methionine with OH radicals and hydroxycinnamic acid (HCA) derivatives, riboflavin (RF) or flavin adenine dinucleotide (FAD), respectively. The HCA derivatives, such as caffeic acid, ferulic acid, sinapic acid and chlorogenic acid, widely distributed phenolic acids in fruit and vegetables, have been identified as good antioxidants previously can rapidly and efficiently repair oxidizing three-electron-bond complexes via electron transfer. RF and FAD can oxidize reducing alpha-amino radicals derived from methionine. The electron transfer rate constants approximately 10(9) dm3 x mol(-1)x s(-1) were determined by following the build-up kinetics of species produced.
The technique of pulse radiolysis with spectrophotometric detection has been used to investigate the possibility of electron transfer reactions between oxidizing sulfur-sulfur three-electron-bond complexes (Met2/S thereforeS+), or reducing alpha-amino radicals (CH3SCH2CH2CH.NH2) derived from reaction of methionine with OH radicals and hydroxycinnamic acid (HCA) derivatives, riboflavin (RF) or flavin adenine dinucleotide (FAD), respectively. The HCA derivatives, such as caffeic acid, ferulic acid, sinapic acid and chlorogenic acid, widely distributed phenolic acids in fruit and vegetables, have been identified as good antioxidants previously can rapidly and efficiently repair oxidizing three-electron-bond complexes via electron transfer. RF and FAD can oxidize reducing alpha-amino radicals derived from methionine. The electron transfer rate constants approximately 10(9) dm3 x mol(-1)x s(-1) were determined by following the build-up kinetics of species produced.
Author Lu, Changyuan
Yao, Side
Lin, Nianyun
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Issue 1
Keywords Riboflavin
Electron transfer
Flavin adenine dinucleotide
Pulse radiolysis
Hydroxycinnamic acid derivative
Methionine
Language English
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Snippet The technique of pulse radiolysis with spectrophotometric detection has been used to investigate the possibility of electron transfer reactions between...
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SubjectTerms Antioxidants - chemistry
Antioxidants - pharmacology
Coumaric Acids - chemistry
Coumaric Acids - pharmacology
Electron transfer
Electron Transport - drug effects
Flavin adenine dinucleotide
Flavin-Adenine Dinucleotide - pharmacology
Free Radical Scavengers - pharmacology
Free Radicals - chemistry
Hydroxycinnamic acid derivative
Hydroxyl Radical - chemistry
In Vitro Techniques
Methionine
Methionine - chemistry
Methionine - metabolism
Oxidation-Reduction
Pulse Radiolysis
Riboflavin
Riboflavin - pharmacology
Solutions
Spectrophotometry
Sulfur - chemistry
Water
Title Studies on reactions of oxidizing sulfur–sulfur three-electron-bond complexes and reducing α-amino radicals derived from OH reaction with methionine in aqueous solution
URI https://dx.doi.org/10.1016/S0304-4165(00)00174-4
https://www.ncbi.nlm.nih.gov/pubmed/11342257
https://www.proquest.com/docview/70817159
Volume 1525
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