Mechanisms of reaction of benzo(a)pyrene-7,8-diol-9,10-epoxide with DNA in aqueous solutions

Nicholas Geacintov, Hanina Hibshoosh, Victor Ibanez, Maurice J. Benjamin, Ronald G. Harvey

Research output: Contribution to journalArticle

Abstract

The physical and chemical reaction pathways of the metabolite model compound benzo(a)pyrene-7,8-diol-9,10-epoxide (BPDE) in aqueous (double-stranded) DNA solutions was investigated as a function of temperature (0-30 ° C). pH (7.0-9.5). sodium chloride concentration (0-1.5M) and DNA concentration in order to clarify the relationships between the multiple reaction mechanisms of this diol epoxide in the presence of nucleic acids. The reaction pathways are (1) noncovalent intercalative complex formation with DNA, characterized by the equilibrium constant K, andXb the fraction of molecules physically bound; (2) accelerated hydrolysis of BPDE bound to DNA; (3) covalent binding to DNA; and (4) hydrolysis of free BPDE (kh). The DNA-induced hydrolysis of BPDE to tetraols and the covalent binding to DNA are parallel pseudo-first-order reactions. Following the rapid (millisecond time scale) noncovalent complex formation between BPDE and DNA, a much slower ( - minutes) H+-dependent (either specific or general acid catalysis) formation of a DNA-bound triol carbonium ion (rate constant k3) occurs. At pH 7.0 the activation energy of k3 is 8.7 ± 0.9 kcal mol, which is lower than the activation en of hydrolysis of free BPDE in buffer solution (14.2 ± 0.7 kcal mol). and which thus partially accounts for the acceleration of hydrolysis of BPDE upon complexation with DNA. The formation of the triol carbonium ion is followed by a rapid reaction with either water to form tetraols (rate constant kT), or covalent binding to DNA (kc). The fraction of BPDE molecules which undergo covalent binding is fcov= kc/(kc + kT = 0.10 and is independent of the overall BPDE reaction rate constant k= kh(1-Xb) + k3Xb if Xb→ 1.0, or is independent of Xb as long as k3Xb ≫ kh(1-Xb). Thus. at Xb = 0.9, fcov is independent of pH (7.0-9.5) even though k exhibits a 70-fold variation in this pH range and k → khabove pH 9 (k3 = kh) Similarly. fcov is independent of temperature (0-30 ° C). while k varies by a factor of approx. 3. In the range of 0-1.5 M NaCl, fcov decreases from 0.10 to 0.04. These variations are attributed to a combination of salt-induced variations in the factors k3 Xb and the ratio kc/kT.

Original languageEnglish (US)
Pages (from-to)121-133
Number of pages13
JournalBiophysical Chemistry
Volume20
Issue number1-2
DOIs
StatePublished - 1984

Fingerprint

7,8-Dihydro-7,8-dihydroxybenzo(a)pyrene 9,10-oxide
epoxy compounds
pyrenes
deoxyribonucleic acid
aqueous solutions
DNA
Hydrolysis
hydrolysis
triols
Rate constants
Ions
Molecules
Temperature
Epoxy Compounds
Equilibrium constants
metabolites
Metabolites
Complexation
Catalysis
nucleic acids

Keywords

  • Benzo(a)pyrene-7,8-diol-9.10-epoxide
  • Binding
  • DNA
  • Hydrolysis
  • Reaction mechanism

ASJC Scopus subject areas

  • Biochemistry
  • Biophysics
  • Physical and Theoretical Chemistry

Cite this

Mechanisms of reaction of benzo(a)pyrene-7,8-diol-9,10-epoxide with DNA in aqueous solutions. / Geacintov, Nicholas; Hibshoosh, Hanina; Ibanez, Victor; Benjamin, Maurice J.; Harvey, Ronald G.

In: Biophysical Chemistry, Vol. 20, No. 1-2, 1984, p. 121-133.

Research output: Contribution to journalArticle

Geacintov, Nicholas ; Hibshoosh, Hanina ; Ibanez, Victor ; Benjamin, Maurice J. ; Harvey, Ronald G. / Mechanisms of reaction of benzo(a)pyrene-7,8-diol-9,10-epoxide with DNA in aqueous solutions. In: Biophysical Chemistry. 1984 ; Vol. 20, No. 1-2. pp. 121-133.
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abstract = "The physical and chemical reaction pathways of the metabolite model compound benzo(a)pyrene-7,8-diol-9,10-epoxide (BPDE) in aqueous (double-stranded) DNA solutions was investigated as a function of temperature (0-30 ° C). pH (7.0-9.5). sodium chloride concentration (0-1.5M) and DNA concentration in order to clarify the relationships between the multiple reaction mechanisms of this diol epoxide in the presence of nucleic acids. The reaction pathways are (1) noncovalent intercalative complex formation with DNA, characterized by the equilibrium constant K, andXb the fraction of molecules physically bound; (2) accelerated hydrolysis of BPDE bound to DNA; (3) covalent binding to DNA; and (4) hydrolysis of free BPDE (kh). The DNA-induced hydrolysis of BPDE to tetraols and the covalent binding to DNA are parallel pseudo-first-order reactions. Following the rapid (millisecond time scale) noncovalent complex formation between BPDE and DNA, a much slower ( - minutes) H+-dependent (either specific or general acid catalysis) formation of a DNA-bound triol carbonium ion (rate constant k3) occurs. At pH 7.0 the activation energy of k3 is 8.7 ± 0.9 kcal mol, which is lower than the activation en of hydrolysis of free BPDE in buffer solution (14.2 ± 0.7 kcal mol). and which thus partially accounts for the acceleration of hydrolysis of BPDE upon complexation with DNA. The formation of the triol carbonium ion is followed by a rapid reaction with either water to form tetraols (rate constant kT), or covalent binding to DNA (kc). The fraction of BPDE molecules which undergo covalent binding is fcov= kc/(kc + kT = 0.10 and is independent of the overall BPDE reaction rate constant k= kh(1-Xb) + k3Xb if Xb→ 1.0, or is independent of Xb as long as k3Xb ≫ kh(1-Xb). Thus. at Xb = 0.9, fcov is independent of pH (7.0-9.5) even though k exhibits a 70-fold variation in this pH range and k → khabove pH 9 (k3 = kh) Similarly. fcov is independent of temperature (0-30 ° C). while k varies by a factor of approx. 3. In the range of 0-1.5 M NaCl, fcov decreases from 0.10 to 0.04. These variations are attributed to a combination of salt-induced variations in the factors k3 Xb and the ratio kc/kT.",
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N2 - The physical and chemical reaction pathways of the metabolite model compound benzo(a)pyrene-7,8-diol-9,10-epoxide (BPDE) in aqueous (double-stranded) DNA solutions was investigated as a function of temperature (0-30 ° C). pH (7.0-9.5). sodium chloride concentration (0-1.5M) and DNA concentration in order to clarify the relationships between the multiple reaction mechanisms of this diol epoxide in the presence of nucleic acids. The reaction pathways are (1) noncovalent intercalative complex formation with DNA, characterized by the equilibrium constant K, andXb the fraction of molecules physically bound; (2) accelerated hydrolysis of BPDE bound to DNA; (3) covalent binding to DNA; and (4) hydrolysis of free BPDE (kh). The DNA-induced hydrolysis of BPDE to tetraols and the covalent binding to DNA are parallel pseudo-first-order reactions. Following the rapid (millisecond time scale) noncovalent complex formation between BPDE and DNA, a much slower ( - minutes) H+-dependent (either specific or general acid catalysis) formation of a DNA-bound triol carbonium ion (rate constant k3) occurs. At pH 7.0 the activation energy of k3 is 8.7 ± 0.9 kcal mol, which is lower than the activation en of hydrolysis of free BPDE in buffer solution (14.2 ± 0.7 kcal mol). and which thus partially accounts for the acceleration of hydrolysis of BPDE upon complexation with DNA. The formation of the triol carbonium ion is followed by a rapid reaction with either water to form tetraols (rate constant kT), or covalent binding to DNA (kc). The fraction of BPDE molecules which undergo covalent binding is fcov= kc/(kc + kT = 0.10 and is independent of the overall BPDE reaction rate constant k= kh(1-Xb) + k3Xb if Xb→ 1.0, or is independent of Xb as long as k3Xb ≫ kh(1-Xb). Thus. at Xb = 0.9, fcov is independent of pH (7.0-9.5) even though k exhibits a 70-fold variation in this pH range and k → khabove pH 9 (k3 = kh) Similarly. fcov is independent of temperature (0-30 ° C). while k varies by a factor of approx. 3. In the range of 0-1.5 M NaCl, fcov decreases from 0.10 to 0.04. These variations are attributed to a combination of salt-induced variations in the factors k3 Xb and the ratio kc/kT.

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