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Appl Environ Microbiol ; 76(21): 7109-15, 2010 Nov.
Article in English | MEDLINE | ID: mdl-20851974

ABSTRACT

Industrial penicillin production levels by the filamentous fungus Penicillium chrysogenum increased dramatically by classical strain improvement. High-yielding strains contain multiple copies of the penicillin biosynthetic gene cluster that encodes three key enzymes of the ß-lactam biosynthetic pathway. We have analyzed the gene cluster dose effect on penicillin production using the high-yielding P. chrysogenum strain DS17690 that was cured from its native clusters. The amount of penicillin V produced increased with the penicillin biosynthetic gene cluster number but was saturated at high copy numbers. Likewise, transcript levels of the biosynthetic genes pcbAB [δ-(l-α-aminoadipyl)-l-cysteinyl-d-valine synthetase], pcbC (isopenicillin N synthase), and penDE (acyltransferase) correlated with the cluster copy number. Remarkably, the protein level of acyltransferase, which localizes to peroxisomes, was saturated already at low cluster copy numbers. At higher copy numbers, intracellular levels of isopenicillin N increased, suggesting that the acyltransferase reaction presents a limiting step at a high gene dose. Since the number and appearance of the peroxisomes did not change significantly with the gene cluster copy number, we conclude that the acyltransferase activity is limiting for penicillin biosynthesis at high biosynthetic gene cluster copy numbers. These results suggest that at a high penicillin production level, productivity is limited by the peroxisomal acyltransferase import activity and/or the availability of coenzyme A (CoA)-activated side chains.


Subject(s)
Gene Dosage/genetics , Multigene Family/genetics , Penicillins/biosynthesis , Penicillium chrysogenum/genetics , Acyltransferases/genetics , Acyltransferases/metabolism , Gene Expression/genetics , Multigene Family/physiology , Oxidoreductases/genetics , Oxidoreductases/metabolism , Penicillin V/metabolism , Penicillin-Binding Proteins/genetics , Penicillin-Binding Proteins/metabolism , Penicillins/metabolism , Penicillium chrysogenum/metabolism , Peptide Synthases/genetics , Peptide Synthases/metabolism , Polymerase Chain Reaction
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