Matching the proteome to the genome: the microbody of penicillin-producing Penicillium chrysogenum cellsKiel, J. A. K. W., van den Berg, M. A., Fusetti, F., Poolman, B., Bovenberg, R. A. L., Veenhuis, M. & van der Klei, I. J., May-2009, In : FUNCTIONAL & INTEGRATIVE GENOMICS. 9, 2, p. 167-184 18 p.
Research output: Contribution to journal › Article › Academic › peer-review
In the filamentous fungus Penicillium chrysogenum, microbodies are essential for penicillin biosynthesis. To better understand the role of these organelles in antibiotics production, we determined the matrix enzyme contents of P. chrysogenum microbodies. Using a novel in silico approach, we first obtained a catalogue of 200 P. chrysogenum proteins with putative microbody targeting signals (PTSs). This included two orthologs of proteins involved in cephalosporin biosynthesis, which we demonstrate to be bona fide microbody matrix constituents. Subsequently, we performed a proteomics based inventory of P. chrysogenum microbody matrix proteins using nano-LC-MS/MS analysis. We identified 89 microbody proteins, 79 with a PTS, including the two known microbody-borne penicillin biosynthesis enzymes, isopenicillin N:acyl CoA acyltransferase and phenylacetyl-CoA ligase. Comparative analysis revealed that 69 out of 79 PTS proteins identified experimentally were in the reference list. A prominent microbody protein was identified as a novel fumarate reductase-cytochrome b5 fusion protein, which contains an internal PTS2 between the two functional domains. We show that this protein indeed localizes to P. chrysogenum microbodies.
|Number of pages||18|
|Journal||FUNCTIONAL & INTEGRATIVE GENOMICS|
|Publication status||Published - May-2009|
- beta-Lactam antibiotics, Filamentous fungus, In silico analysis, Proteomics, Peroxisome, ACYL-COA DEHYDROGENASE, ASPERGILLUS-NIDULANS, HANSENULA-POLYMORPHA, PEROXISOME BIOGENESIS, SACCHAROMYCES-CEREVISIAE, ASPARTATE-AMINOTRANSFERASE, STATISTICAL-MODEL, DATABASE SEARCH, ISOPENICILLIN-N, BETA-OXIDATION