2014
DOI: 10.1007/s11274-014-1721-1
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Comparative gene expression profiling reveals key changes in expression levels of cephalosporin C biosynthesis and transport genes between low and high-producing strains of Acremonium chrysogenum

Abstract: Transcript levels of several key genes responsible for cephalosporin C (CPC) biosynthesis and transport have been determined using qPCR analysis of Acremonium chrysogenum strains differing more than 100-fold in the levels of CPC production. The expression of genes involved in the final steps of CPC production was significantly increased in the high-producing RNCM F-4081D strain compared to the wild-type ATCC 11550 strain. Different dynamics in the course of cultivation was observed for the genes known to be in… Show more

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Cited by 18 publications
(34 citation statements)
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“…Identification of bacteria and fungi was performed by sequencing 16S rDNA or internal transcribed spacer (ITS) regions, respectively. Genomic DNA was isolated as described previously [20] with some modifications (Materials and methods 1.2 in S1 File). Bacterial 16S rDNA V3/V4 region was amplified using primers 341F (5'-CCTACGGGAGGCAGCAG-3') [21] and R806 (5'-GGACTACHVGGGTWTCTAA-3') [22].…”
Section: Characterization Of Microorganisms In Initial Samples Cultumentioning
confidence: 99%
“…Identification of bacteria and fungi was performed by sequencing 16S rDNA or internal transcribed spacer (ITS) regions, respectively. Genomic DNA was isolated as described previously [20] with some modifications (Materials and methods 1.2 in S1 File). Bacterial 16S rDNA V3/V4 region was amplified using primers 341F (5'-CCTACGGGAGGCAGCAG-3') [21] and R806 (5'-GGACTACHVGGGTWTCTAA-3') [22].…”
Section: Characterization Of Microorganisms In Initial Samples Cultumentioning
confidence: 99%
“…An increase in the production of the target SM by 100-to 1000-fold and the elimination of spin-off products under the fermentation conditions in the improved fungal strains ( Figure 2B) are associated with two main molecular events, the upregulation of genes from target BGC and the knockout of genes from alternative BGC [27,33,41,42]. Since the expression of BGC genes is controlled by the pathway-specific regulation [27,43,44], global regulation [45,46], and global regulation of SM [47][48][49][50], the SCI programs are accompanied by changes in such controls.…”
Section: The Molecular Mechanisms Of Sm Overproduction In Filamentousmentioning
confidence: 99%
“…The conversion from DAC to CPC is catalyzed by deacetylcephalosporin-C acetyltransferase enzyme (CefG; EC 2.3.1.175) by, occurs in the cytoplasm [59] and is utilizes one molecule of cytoplasmic acetyl-CoA per reaction. In HY strains the CPC production increased 200-to 300-fold and the expression from BGC for CPC (cef genes) upregulated 20-to 300-fold [41]. In this case the acetyl-CoA content may be depleted in some HY strains [57,58].…”
Section: The Molecular Mechanisms Of Sm Overproduction In Filamentousmentioning
confidence: 99%
“…The strains were cultivated on CD medium for 48 h at 26 • C and inoculated into ten volumes of CD medium. The fermentation was carried out for 120 h at 26 • C in 250-mL Erlenmeyer flasks on a CERTOMAT BS-1 shaker (Sartorius, Germany) at 230 rpm, as described earlier [42]. After 24 h of culture, 1 mL aliquots were removed, fungi were separated by centrifugation (15 min, 14,000 g) and washed with H 2 O (3 × 2 mL).…”
Section: Determination Of Polyamine Content In the Fungimentioning
confidence: 99%