Oxygen activation during oxidation of methoxyhydroquinones by laccase from Pleurotus eryngii.

Q + O(2)(*-)). As this reaction is reversible, its existence was first noted in studies of the effect of systems consuming and producing O(2)(*-) on quinone formation rates. Then, the production of H(2)O(2) in laccase reactions, as a consequence of O(2)(*-) dismutation, confirmed that semiquinones autoxidized. The highest H(2)O(2) levels were obtained with DBQH(2), indicating that DBQ(*-) autoxidized to a greater extent than did MBQ(*-). Besides undergoing autoxidation, semiquinones were found to be transformed into quinones via dismutation and laccase oxidation. Two ways of favoring semiquinone autoxidation over dismutation and laccase oxidation were increasing the rate of O(2)(*-) consumption with superoxide dismutase (SOD) and recycling of quinones with diaphorase (a reductase catalyzing the divalent reduction of quinones). These two strategies made the laccase reaction conditions more natural, since O(2)(*-), besides undergoing dismutation, reacts with Mn(2+), Fe(3+), and aromatic radicals. In addition, quinones are continuously reduced by the mycelium of white-rot fungi. The presence of SOD in laccase reactions increased the extent of autoxidation of 100 microM concentrations of MBQ(*-) and DBQ(*-) from 4.5 to 30.6% and from 19.6 to 40.0%, respectively. With diaphorase, the extent of MBQ(*-) autoxidation rose to 13.8% and that of DBQ(*-) increased to 39.9%. -->
References: Biochem J. 1992 Sep 1;286 ( Pt 2):481-90. (PMID: 1530580)
Biochem Biophys Res Commun. 1983 Aug 12;114(3):1077-83. (PMID: 6615503)
Biochem Biophys Res Commun. 1991 Apr 15;176(1):269-75. (PMID: 2018522)
Proc Natl Acad Sci U S A. 1993 Feb 15;90(4):1242-6. (PMID: 8433984)
Appl Environ Microbiol. 1997 Jun;63(6):2166-74. (PMID: 9172335)
Appl Environ Microbiol. 1983 Nov;46(5):1140-5. (PMID: 16346420)
FEBS Lett. 1990 Jul 2;267(1):99-102. (PMID: 2365094)
FEMS Microbiol Lett. 1997 Nov 1;156(1):9-14. (PMID: 9368354)
Free Radic Biol Med. 1989;7(4):435-77. (PMID: 2691341)
Appl Environ Microbiol. 1994 Aug;60(8):2811-7. (PMID: 16349349)
Arch Biochem Biophys. 1989 Apr;270(1):404-9. (PMID: 2930198)
Biochemistry (Mosc). 1998 Feb;63(2):200-6. (PMID: 9526115)
Arch Biochem Biophys. 1997 Mar 1;339(1):190-9. (PMID: 9056249)
Biochem J. 1985 Jun 15;228(3):557-64. (PMID: 2992449)
Arch Biochem Biophys. 1993 May;302(2):447-54. (PMID: 8387747)
Science. 1983 Aug 12;221(4611):661-3. (PMID: 17787736)
Eur J Biochem. 1996 Apr 15;237(2):424-32. (PMID: 8647081)
FEBS Lett. 1979 Dec 1;108(1):229-32. (PMID: 520550)
Appl Environ Microbiol. 1994 Jun;60(6):1783-8. (PMID: 8031078)
J Biol Chem. 1985 Jul 15;260(14):8348-53. (PMID: 2989288)
Arch Biochem Biophys. 1982 Apr 1;214(2):452-63. (PMID: 6284026)
Eur J Biochem. 1992 Oct 15;209(2):603-11. (PMID: 1425667)
Appl Environ Microbiol. 1998 Jan;64(1):68-73. (PMID: 16349495)
Biochemistry. 1990 Nov 20;29(46):10475-80. (PMID: 2176868)
J Bacteriol. 1987 May;169(5):2195-201. (PMID: 3553159)
Arch Biochem Biophys. 1992 Nov 1;298(2):480-5. (PMID: 1329659)
FEBS Lett. 1992 Mar 24;299(1):107-10. (PMID: 1312029)
Annu Rev Microbiol. 1987;41:465-505. (PMID: 3318677)
FEBS Lett. 1996 Aug 5;391(1-2):144-8. (PMID: 8706903)
Appl Environ Microbiol. 1999 Oct;65(10):4458-63. (PMID: 10508075)
Chem Biol Interact. 1990;73(1):53-76. (PMID: 2105855)
Experientia. 1981 Dec 15;37(12):1233-41. (PMID: 7035210)
Substance Nomenclature: 0 (Hydroquinones)
BBX060AN9V (Hydrogen Peroxide)
EC 1.- (Oxidoreductases)
EC 1.10.3.2 (Laccase)
EC 1.15.1.1 (Superoxide Dismutase)
EC 1.8.1.4 (Dihydrolipoamide Dehydrogenase)
S88TT14065 (Oxygen)
Entry Date(s): Date Created: 20000105 Date Completed: 20000209 Latest Revision: 20210526
Update Code: 20231215
PubMed Central ID: PMC91801
DOI: 10.1128/AEM.66.1.170-175.2000
PMID: 10618219
Autor: Guillén F; Centro de Investigaciones Biológicas, Consejo Superior de Investigaciones Científicas, E-28006 Madrid, Spain. guillen@cib.csic.es, Muñoz C, Gómez-Toribio V, Martínez AT, Jesús Martínez M
Jazyk: angličtina
Zdroj: Applied and environmental microbiology [Appl Environ Microbiol] 2000 Jan; Vol. 66 (1), pp. 170-5.
DOI: 10.1128/AEM.66.1.170-175.2000
Abstrakt: Oxygen activation during oxidation of the lignin-derived hydroquinones 2-methoxy-1,4-benzohydroquinone (MBQH(2)) and 2, 6-dimethoxy-1,4-benzohydroquinone (DBQH(2)) by laccase from Pleurotus eryngii was examined. Laccase oxidized DBQH(2) more efficiently than it oxidized MBQH(2); both the affinity and maximal velocity of oxidation were higher for DBQH(2) than for MBQH(2). Autoxidation of the semiquinones produced by laccase led to the activation of oxygen, producing superoxide anion radicals (Q(*-) + O(2) <--> Q + O(2)(*-)). As this reaction is reversible, its existence was first noted in studies of the effect of systems consuming and producing O(2)(*-) on quinone formation rates. Then, the production of H(2)O(2) in laccase reactions, as a consequence of O(2)(*-) dismutation, confirmed that semiquinones autoxidized. The highest H(2)O(2) levels were obtained with DBQH(2), indicating that DBQ(*-) autoxidized to a greater extent than did MBQ(*-). Besides undergoing autoxidation, semiquinones were found to be transformed into quinones via dismutation and laccase oxidation. Two ways of favoring semiquinone autoxidation over dismutation and laccase oxidation were increasing the rate of O(2)(*-) consumption with superoxide dismutase (SOD) and recycling of quinones with diaphorase (a reductase catalyzing the divalent reduction of quinones). These two strategies made the laccase reaction conditions more natural, since O(2)(*-), besides undergoing dismutation, reacts with Mn(2+), Fe(3+), and aromatic radicals. In addition, quinones are continuously reduced by the mycelium of white-rot fungi. The presence of SOD in laccase reactions increased the extent of autoxidation of 100 microM concentrations of MBQ(*-) and DBQ(*-) from 4.5 to 30.6% and from 19.6 to 40.0%, respectively. With diaphorase, the extent of MBQ(*-) autoxidation rose to 13.8% and that of DBQ(*-) increased to 39.9%.
Databáze: MEDLINE