2014
DOI: 10.1007/s11274-014-1721-1
|View full text |Cite
|
Sign up to set email alerts
|

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

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
34
0

Year Published

2016
2016
2023
2023

Publication Types

Select...
7
1

Relationship

0
8

Authors

Journals

citations
Cited by 17 publications
(34 citation statements)
references
References 30 publications
(32 reference statements)
0
34
0
Order By: Relevance
“…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%