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J. Biol. Chem., Vol. 277, Issue 48, 46216-46225, November 29, 2002
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§¶,
§,
,
§, and
§
From the 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
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
-lactam antibiotics.
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.
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