Penicillin biosynthesis: the origin of hydroxy groups in β-lactams derived from unsaturated substrates

التفاصيل البيبلوغرافية
العنوان: Penicillin biosynthesis: the origin of hydroxy groups in β-lactams derived from unsaturated substrates
المؤلفون: Hong-Hoi Ting, Sabine L. Flitsch, Nicholas J. Turner, Robert M. Adlington, Jack E. Baldwin
المصدر: J. Chem. Soc., Chem. Commun.. :1305-1308
بيانات النشر: Royal Society of Chemistry (RSC), 1986.
سنة النشر: 1986
مصطلحات موضوعية: inorganic chemicals, chemistry.chemical_classification, biology, Chemistry, Stereochemistry, Isopenicillin N synthase, Peptide, Cofactor, Enzyme, Oxygen atom, Cephalosporium acremonium, β lactams, polycyclic compounds, biology.protein, Molecular Medicine, Penicillin biosynthesis
الوصف: Two unsaturated peptide substrates were each cyclised by the enzyme isopenicillin N synthase (IPNS) from Cephalosporium acremonium CO 728 simultaneously to both desaturated and hydroxylated β-lactam products whose hydroxy groups have been shown to derive their oxygen atom from the cosubstrate dioxygen; a working hypothesis involving iron–oxo species is proposed to explain this phenomenon.
تدمد: 0022-4936
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::0fa48a231f6a17b59ab2fb66851a7f15
https://doi.org/10.1039/c39860001305
رقم الأكسشن: edsair.doi...........0fa48a231f6a17b59ab2fb66851a7f15
قاعدة البيانات: OpenAIRE