laccase and Leukemia-P388

laccase has been researched along with Leukemia-P388* in 1 studies

Other Studies

1 other study(ies) available for laccase and Leukemia-P388

ArticleYear
Oxidative coupling of mithramycin and hydroquinone catalyzed by copper oxidases and benzoquinone. Implications for the mechanism of action of aureolic acid antibiotics.
    Bioorganic & medicinal chemistry, 1994, Volume: 2, Issue:6

    The copper oxidases human ceruloplasmin and Polyporous anceps laccase catalyze the oxidative coupling of mithramycin (1) and its aglycone chromomycinone (2) with p-hydroquinone to form new mithramycin-hydroquinone (3) and chromomycinone-hydroquinone adducts (4), respectively. Similar adducts could be formed by the nonenzymatic mimic of this reaction using benzoquinone and these aureolic acids in buffer solutions. FABMS of 3 indicated that the hydroquinone moiety was attached to the aureolic acid aglycone. Acid hydrolysis of 3 yielded a compound with the same chromatographic and spectroscopic characteristics as 4. Structure elucidation of 4 by NMR and MS revealed that the hydroquinone was attached to the C-5 position of the aglycone. NMR evidence indicated that 4 consisted of a mixture of ortho-substituted biphenyl rotamers. The mechanism of the copper oxidase catalyzed adduct formation reaction is presumed to involve radical formation through hydrogen removal at the 8-phenolic position, radical isomerization, and coupling with semiquinone radical also formed during enzymatic and nonenzymatic incubations. Identification of the covalent-hydroquinone adduct provides evidence that aureolic acid antibiotics can be metabolically converted to reactive radical intermediates, and it establishes the C-5 position of aureolic acid as an enzymatically reactive site. Unlike mithramycin, the mithramycin-hydroquinone adducts was inactive in the in vivo P388 leukemic antitumor test system.

    Topics: Animals; Antibiotics, Antineoplastic; Benzoquinones; Catalysis; Ceruloplasmin; Drug Evaluation, Preclinical; Humans; Hydroquinones; Laccase; Leukemia P388; Male; Mice; Mice, Inbred Strains; Molecular Structure; Oxidoreductases; Plicamycin; Polyporaceae; Spectrometry, Mass, Fast Atom Bombardment

1994