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pubmed-article:7764842pubmed:abstractTextThe effect of phenylacetic acid (PAA) and several analogs on the activity of isopenicillin N synthase (IPNS) and acyl-CoA: 6-APA acyltransferase (AT) from Penicillium chrysogenum Wis 54-1255 has been tested. Whereas the substitution on the ring of a hydrogen atom by hydroxy-, methyl- or methoxy- groups did not cause any effect, the presence of halogens (Cl or Br) at positions 3 and/or 4 of PAA strongly inhibited these two enzymes. The replacement of hydrogen atoms by fluorine in certain positions also caused inhibition, but to a lesser extent.lld:pubmed
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pubmed-article:7764842pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:7764842pubmed:articleTitleInhibition of penicillin biosynthetic enzymes by halogen derivatives of phenylacetic acid.lld:pubmed
pubmed-article:7764842pubmed:affiliationDepartamento de Bioquímica y Biología Molecular, Facultad de Veterinaria, Universidad de León, Spain.lld:pubmed
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pubmed-article:7764842pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed