Literature DB >> 8106341

Exogenous methionine increases levels of mRNAs transcribed from pcbAB, pcbC, and cefEF genes, encoding enzymes of the cephalosporin biosynthetic pathway, in Acremonium chrysogenum.

J Velasco1, S Gutierrez, F J Fernandez, A T Marcos, C Arenos, J F Martin.   

Abstract

Methionine stimulated cephalosporin production in cultures of three different strains of Acremonium chrysogenum when added either at inoculation time or at 72 h to cells grown previously in the absence of methionine. When methionine was added at 72 h, the stimulation of cephalosporin biosynthesis was observed only 12 h later and required de novo protein synthesis. Methionine increased the levels of enzymes (isopenicillin N synthase and deacetylcephalosporin C acetyltransferase) expressed from genes (pcbC and cefG, respectively) located in the two clusters of cephalosporin biosynthesis genes in the wild-type A. chrysogenum strain and also in the two improved strains, CW19 and C10. Methionine-supplemented cells showed higher levels of transcripts of the four known genes (pcbAB, pcbC, cefEF and, to a slight extent, cefG) of the cephalosporin biosynthetic pathway than cells grown in the absence of methionine. The levels of the cefG transcript were much lower than those of the pcbAB, pcbC, and cefEF transcripts. The induction by methionine of transcription of the four cephalosporin biosynthesis genes and the known effect of this amino acid on the differentiation of A. chrysogenum indicate that methionine exerts a pleiotropic effect that coordinately regulates cephalosporin biosynthesis and differentiation.

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Year:  1994        PMID: 8106341      PMCID: PMC205148          DOI: 10.1128/jb.176.4.985-991.1994

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  24 in total

1.  A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding.

Authors:  M M Bradford
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2.  A new DNA binding and dimerization motif in immunoglobulin enhancer binding, daughterless, MyoD, and myc proteins.

Authors:  C Murre; P S McCaw; D Baltimore
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Review 4.  The biosynthesis of sulfur-containing beta-lactam antibiotics.

Authors:  J Nüesch; J Heim; H J Treichler
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5.  The two positively acting regulatory proteins PHO2 and PHO4 physically interact with PHO5 upstream activation regions.

Authors:  K Vogel; W Hörz; A Hinnen
Journal:  Mol Cell Biol       Date:  1989-05       Impact factor: 4.272

6.  Isolation, sequence determination and expression in Escherichia coli of the isopenicillin N synthetase gene from Cephalosporium acremonium.

Authors:  S M Samson; R Belagaje; D T Blankenship; J L Chapman; D Perry; P L Skatrud; R M VanFrank; E P Abraham; J E Baldwin; S W Queener
Journal:  Nature       Date:  1985 Nov 14-20       Impact factor: 49.962

7.  Carbon catabolite regulation of the conversion of penicillin N into cephalosporin C.

Authors:  D M Martin-Zanca; J F Martín
Journal:  J Antibiot (Tokyo)       Date:  1983-06       Impact factor: 2.649

8.  Isopenicillin N synthetase of Penicillium chrysogenum, an enzyme that converts delta-(L-alpha-aminoadipyl)-L-cysteinyl-D-valine to isopenicillin N.

Authors:  F R Ramos; M J López-Nieto; J F Martín
Journal:  Antimicrob Agents Chemother       Date:  1985-03       Impact factor: 5.191

9.  Cloning, sequence analysis and transcriptional study of the isopenicillin N synthase of Penicillium chrysogenum AS-P-78.

Authors:  J L Barredo; J M Cantoral; E Alvarez; B Díez; J F Martín
Journal:  Mol Gen Genet       Date:  1989-03

Review 10.  Clusters of genes for the biosynthesis of antibiotics: regulatory genes and overproduction of pharmaceuticals.

Authors:  J F Martin
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  13 in total

1.  Molecular characterization of the Acremonium chrysogenum cefG gene product: the native deacetylcephalosporin C acetyltransferase is not processed into subunits.

Authors:  J Velasco; S Gutierrez; S Campoy; J F Martin
Journal:  Biochem J       Date:  1999-02-01       Impact factor: 3.857

2.  Molecular characterization of three loss-of-function mutations in the isopenicillin N-acyltransferase gene (penDE) of Penicillium chrysogenum.

Authors:  F J Fernández; S Gutierrez; J Velasco; E Montenegro; A T Marcos; J F Martín
Journal:  J Bacteriol       Date:  1994-08       Impact factor: 3.490

3.  Uric acid is a genuine metabolite of Penicillium cyclopium and stimulates the expression of alkaloid biosynthesis in this fungus.

Authors:  Florian Helbig; Jörg Steighardt; Werner Roos
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4.  A homologue of the Aspergillus velvet gene regulates both cephalosporin C biosynthesis and hyphal fragmentation in Acremonium chrysogenum.

Authors:  Jacqueline Dreyer; Heiko Eichhorn; Ernst Friedlin; Hubert Kürnsteiner; Ulrich Kück
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5.  Regulation of the Aspergillus nidulans penicillin biosynthesis gene acvA (pcbAB) by amino acids: implication for involvement of transcription factor PACC.

Authors:  K Then Bergh; A A Brakhage
Journal:  Appl Environ Microbiol       Date:  1998-03       Impact factor: 4.792

Review 6.  Molecular regulation of beta-lactam biosynthesis in filamentous fungi.

Authors:  A A Brakhage
Journal:  Microbiol Mol Biol Rev       Date:  1998-09       Impact factor: 11.056

7.  Expression of the Acremonium chrysogenum cefT gene in Penicillum chrysogenum indicates that it encodes an hydrophilic beta-lactam transporter.

Authors:  Ricardo V Ullán; Fernando Teijeira; Juan F Martín
Journal:  Curr Genet       Date:  2008-07-31       Impact factor: 3.886

8.  Targeted inactivation of the mecB gene, encoding cystathionine-gamma-lyase, shows that the reverse transsulfuration pathway is required for high-level cephalosporin biosynthesis in Acremonium chrysogenum C10 but not for methionine induction of the cephalosporin genes.

Authors:  G Liu; J Casqueiro; O Bañuelos; R E Cardoza; S Gutiérrez; J F Martín
Journal:  J Bacteriol       Date:  2001-03       Impact factor: 3.490

9.  Expression studies with the bidirectional pcbAB-pcbC promoter region from Acremonium chrysogenum using reporter gene fusions.

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Review 10.  Expression of genes and processing of enzymes for the biosynthesis of penicillins and cephalosporins.

Authors:  J F Martín; S Gutiérrez; F J Fernández; J Velasco; F Fierro; A T Marcos; K Kosalkova
Journal:  Antonie Van Leeuwenhoek       Date:  1994       Impact factor: 2.271

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