Thus, the paralogous genes annotated as crtB2 and crtI2-1 and crtI2-2 are either not functional or not expressed (enough) under the chosen conditions. Complementation analysis of the deletion mutants ΔcrtB and ΔcrtI was chosen to test whether crtB2 and/or crtI2-1/2 encode functional enzymes. Overexpression of crtB2 almost completely complemented the crtB deletion and as HPLC analysis of extracts from C. glutamicum ΔcrtB(pEKEx3-crtB2) indicated accumulation of decaprenoxanthin crtB2 encodes a functional phytoene synthase (AZD1390 solubility dmso Figure 2, Additional file 5: Figure S3). By contrast, overexpression of crtI2-1/2 in C. glutamicum ΔcrtI did not restore the wild-type phenotype

while overexpression of crtI did. Furthermore, while combined expression of crtB2 and crtI in C. glutamicum strain ΔΔ led to an accumulation of lycopene, the combined expression of crtB2 and crtI2-1/2 did not (Additional selleck compound file 6: Figure S4). Thus, whereas no evidence for crtI2-1/2 encoding a phytoene desaturase was found, crtB2 encodes an enzyme active as phytoene synthase. Enhancing lycopene production by overexpression of carotenogenic genes in the lycopene accumulating strain C. glutamicum ΔcrtEb The deletion of the gene crtEb entailed accumulation of lycopene to 0.03 ± 0.01 mg/g CDW in C. glutamicum. To enhance the production of lycopene we focused on improving conversion of GGPP to lycopene. Overexpression of the phytoene synthase gene crtB and/or

the phytoene BMN 673 supplier desaturase gene crtI in C. glutamicum ΔcrtEb (Additional file 3: Table S1) was tested. Whereas crtI overexpression showed no effect on lycopene production (0.02 ± 0.01 mg/g CDW), it could be shown that lycopene accumulation was increased two-fold when crtB was overexpressed (0.06 ± 0.01 mg/g CDW, Figure 4). However, combined overexpression of both genes did not increase the lycopene content significantly (0.04 ± 0.01 mg/g

CDW). Figure 4 Lycopene production PAK5 in C. glutamicum Δ crtEb overexpressing carotenogenic genes. (A) Cell pellets of cultures grown in glucose CGXII minimal medium after consumption of the carbon source. By the overexpression of the indicated carotenogenic genes the intensity of the red color was enhanced. (B) Lycopene concentrations of the cells depicted in A as determined by HPLC analyses of cell extracts. Besides overexpression of crtB, also overexpression of crtE which codes for the geranylgeranyl pyrophosphatase catalyzing the condensation of IPP and DMPP eventually leading to GGPP (Figure 2), increased lycopene production (Figure 4). As a consequence of overproduction of geranylgeranyl pyrophosphatase in C. glutamicum ΔcrtEb, lycopene accumulated to four-fold higher concentrations (0.12 ± 0.01 mg/g CDW). The combined overexpression of crtB and crtE resulted in about 25 fold higher lycopene accumulation (0.8 ± 0.1 mg/g CDW, Figure 4) as compared to C. glutamicum ΔcrtEb. The maximal lycopene concentration of 2.4 ± 0.