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Originally published In Press as doi:10.1074/jbc.M207482200 on September 11, 2002
J. Biol. Chem., Vol. 277, Issue 48, 46216-46225, November 29, 2002
A Novel Epimerization System in Fungal Secondary Metabolism
Involved in the Conversion of Isopenicillin N into Penicillin N in
Acremonium chrysogenum*
Ricardo V.
Ullán §¶,
Javier
Casqueiro §,
Oscar
Bañuelos ,
Francisco J.
Fernández§,
Santiago
Gutiérrez §, and
Juan F.
Martín §
From the Area de Microbiología, Facultad de
Ciencias Biológicas y Ambientales, Universidad de León,
24071 León, Spain and § Instituto de
Biotecnología de León (INBIOTEC), Parque
Científico de León, Avda del Real 1, 24006 León, Spain
The epimerization step that converts
isopenicillin N into penicillin N during cephalosporin biosynthesis has
remained uncharacterized despite its industrial relevance. A
transcriptional analysis of a 9-kb region located downstream of the
pcbC gene revealed the presence of two transcripts that
correspond to the genes named cefD1 and cefD2
encoding proteins with high similarity to long chain acyl-CoA
synthetases and acyl-CoA racemases from Mus musculus, Homo sapiens, and Rattus norvegicus. Both genes
are expressed in opposite orientations from a bidirectional promoter
region. Targeted inactivation of cefD1 and
cefD2 was achieved by the two-marker gene replacement
procedure. Disrupted strains lacked isopenicillin N epimerase activity,
were blocked in cephalosporin C production, and accumulated
isopenicillin N. Complementation in trans of the disrupted
nonproducer mutant with both genes restored epimerase activity and
cephalosporin biosynthesis. However, when cefD1 or cefD2 were introduced separately into the double-disrupted
mutant, no epimerase activity was detected, indicating that the
concerted action of both proteins encoded by cefD1 and
cefD2 is required for epimerization of isopenicillin N into
penicillin N. This epimerization system occurs in eukaryotic cells and
is entirely different from the known epimerization systems involved in
the biosynthesis of bacterial -lactam antibiotics.
*
This work was supported by grants from Biochimie GmbH (the
Novartis group, Austria), Comisión Interministerial de Ciencia y
Tecnología, Spain (Ministry of Education and Science, Madrid) Grant BIO97-0289-C02-01, and Agencia de Desarrollo Económico de
Castilla y León Grant 08-2/99/LE/0001.The costs of publication of this
article were defrayed in part by the
payment of page charges. The article
must therefore be hereby marked
"advertisement" in accordance with 18 U.S.C. Section
1734 solely to indicate this fact.
The nucleotide sequence(s) reported in this paper has been submitted to the GenBankTM/EBI Data Bank with accession number(s) AJ507632.
¶
Recipient of a fellowship of the Diputación de
León (Spain).
To whom correspondence should be addressed. Tel.:
34-987-291505; Fax: 34-987-291506; E-mail: degjmm@unileon.es.
Copyright © 2002 by The American Society for Biochemistry and Molecular Biology, Inc.

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Copyright © 2002 by the American Society for Biochemistry and Molecular Biology.
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