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pubmed-article:2507494pubmed:abstractTextThe phenylacetic acid (PA) transport system of Penicillium chrysogenum is induced by PA, 2-hydroxyphenylacetic and 4-phenylbutyric acids but not by benzoic, phenoxyacetic acid and phenylpropionic acids. Substitution in the aromatic moiety (3-hydroxyphenylacetic, 4-hydroxyphenylacetic acids), replacement of the aromatic moiety by other rings (thiophene-2-acetic acid, indole-3-acetic or indole-3-butyric acids) or the presence of an amino group in the alpha-position (2-aminophenylacetic acid) eliminates inducing activity. 2-Phenylbutyric acid dose not induce the PA transport system indicating that fatty acid-beta-oxidation is needed to generate the authentic regulatory molecule (phenylacetyl-CoA) from 4-phenylbutyric acid. Furthermore, the uptake system synthesized in presence of PA, 2-hydroxyphenylacetic or 4-phenylbutyric acids is under carbon catabolic repression control and is also repressed by L-lysine suggesting that the three molecules induce in P. chrysogenum a single mechanism of transport.lld:pubmed
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pubmed-article:2507494pubmed:pagination1410-5lld:pubmed
pubmed-article:2507494pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:2507494pubmed:articleTitlePhenylacetic acid transport system in Penicillium chrysogenum Wis 54-1255: molecular specificity of its induction.lld:pubmed
pubmed-article:2507494pubmed:affiliationDepartamento de Bioquímica y Biología Molecular, Universidad de León, España.lld:pubmed
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pubmed-article:2507494pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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