Transcriptional and bioinformatic analysis of the 56.8kb DNA region amplified in tandem repeats containing the penicillin gene cluster in Penicillium chrysogenum

被引:54
|
作者
Fierro, Francisco
Garcia-Estrada, Carlos
Castillo, Nancy I.
Rodriguez, Raquel
Velasco-Conde, Tania
Martin, Juan-Francisco
机构
[1] INBIOTEC, Inst Biotecnol Leon, Leon 24006, Spain
[2] Univ Leon, Area Microbiol, Fac CC Biol & Ambientales, E-24071 Leon, Spain
关键词
transcriptional analysis; amplified region; penicillin biosynthesis; gene clusters; precursor biosynthesis; regulatory genes;
D O I
10.1016/j.fgb.2006.03.001
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
High penicillin-producing strains of Penicillium chrysogenum contain 6-14 copies of the three clustered structural biosynthetic genes, pcbAB, pcbC, and penDE [Barredo, J.L., Diez, B., Alvarez, E., Martin, J.F., 1989. Large amplification of a 35-kb DNA fragment carrying two penicillin biosynthetic genes in high penicillin producing strains of Penicillium chrysogenum. Curr. Genet. 16, 453-459; Smith, D.J., Bull, J.H., Edwards, J., Turner, G., 1989. Amplification of the isopenicillin N synthetase gene in a strain of Penicillium chrysogenum producing high levels of penicillin. Mol. Gen. Genet. 216, 492-497.] Barredo et al., 1989; Smith et al., 1989. The cluster is located in a 56.8 kb DNA region bounded by a conserved TGTAAA/T hexanucleotide that undergoes amplification in tandem repeats [Fierro, F., Barredo, J.L., Diez, B., Gutierrez, S., Fernandez, F.J., Martin, J.F., 1995. The penicillin gene cluster is amplified in tandem repeats linked by conserved hexanucleotide sequences. Proc. Natl. Acad. Sci. USA 92, 6200-6204; Newbert, R.W., Barton, B., Greaves, P., Harper, J., Turner, G., 1997. Analysis of a commercially improved Penicillium chrysogenum strain series: involvement of recombinogenic regions in amplification and deletion of the penicillin biosynthesis gene cluster. J. Ind. Microbic]. Biotechnol. 19, 18-27.]. Transcriptional analysis of this amplified region (AR) revealed the presence of at least eight transcripts expressed in penicillin producing conditions. Three of them correspond to the known penicillin biosynthetic genes, pcbA B, pcbC, and penDE. To locate genes related to penicillin precursor formation, or penicillin transport and regulation we have sequenced and analyzed the 56.8 kb amplified region of P. chrysogenum AS-P-78, finding a total of 16 open reading frames. Two of these ORFs have orthologues of known function in the databases. Other ORT's showed similarities to specific domains occurring in different proteins and superfamilies which allowed to infer their probable function. ORFI I encodes a D-amino acid oxidase that might be responsible for the conversion Of D-amino acids in the tripeptide L-alpha-aminoadipyl-L-cysteinyl-D-valine or other beta-lactam intermediates to deaminated by-products. ORF12 encodes a predicted protein with similarity to saccharopine dehydrogenases that seems to be related to biosynthesis of the penicillin precursor alpha-aminoadipic acid. A deletion mutant, P. chrysogenum npe10 lacking the entire AR including ORF12, shows a partial requirement Of L-lysine for growth. ORFI 3 encodes a putative protein containing a Zn(II)2-Cys6 fungal-type DNA-binding domain, probably a transcriptional regulator. Although some of the ORFs in the AR may play roles in increasing penicillin production, none of the 13 ORT's other than pcbAB, pcbC, and penDE seem to be strictly indispensable for penicillin biosynthesis. The genes located in the P. chrysogenum AR have been compared with those found in the Aspergillus nidulans 50 kb DNA region adjacent to the penicillin gene cluster, showing no conservation between these two fungi. (c) 2006 Elsevier Inc. All rights reserved.
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收藏
页码:618 / 629
页数:12
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