Production of α-cuprenene in Xanthophyllomyces dendrorhous: A step closer to a potent terpene biofactory

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Abstract

Background: The red yeast Xanthophyllomyces dendrorhous is a natural producer of the carotenoid astaxanthin. Because of its high flux, the native terpene pathway leading to the production of the tetraterpene is of particular interest as it can be redirected toward the production of other terpene compounds. The genetic tools for the transformation of the yeast with the concurrent knock-out of genes involved in the astaxanthin biosynthesis are made available and here we show that the production of the sesquiterpene α-cuprenene is possible in mutant strains of X. dendrorhous transformed with the Cop6 gene originating from the fungus Coprinus cinereus. For the evaluation of the production levels, we chose to express the same gene and analyze the accumulation of α-cuprenene in Escherichia coli and Saccharomyces cerevisiae, as well. Here we propose that X. dendrorhous is a candidate in the search for the potential platform organism for the production of terpenes.Results: All three X. dendrorhous mutants functionally express the Cop6 gene and accumulate α-cuprenene. The production of α-cuprenene in the red yeast reached 80 mg/L, which represents a far higher concentration compared to the levels obtained in the E. coli and S. cerevisiae mutants. At this expression levels the pool of terpene precursors has not become a limiting factor in the X. dendrorhous mutants since the expression of the Cop6 gene in the genomic rDNA of the yeast allows production of both α-cuprenene and astaxanthin without affecting the growth or the accumulation levels of both compounds.Conclusions: We have shown that X. dendrorhous can produce α-cuprenene, and the results here presented, next to the capability of accumulating at least two more non-native sesquiterpenes, demonstrates the high potential of this yeast to become an interesting terpene-based drugs producer. © 2013 Melillo et al.; licensee BioMed Central Ltd.

Figures

  • Figure 1 Cuprenene production during time course with E. coli pHis8Cop6.
  • Figure 2 Schematic representation of X. dendrorhous mutant strains. (A) In the mutant XdCop6, the native astaxanthin pathway has not been modified but the gene Cop6 has been integrated in the rDNA of the yeast allowing the mutant to produce both astaxanthin and α-cuprenene. (B) In the strain ΔE-Cop6 the Cop6 gene has been inserted in the crtE gene causing the disruption of the carotenoid production at the GGPP synthesis level. (C) When Cop6 is inserted in the crtYB gene, the ΔYB-Cop6 strain is created. While there is still expression of the GGPPS, phytoene cannot be produced anymore, blocking the production of astaxanthin one step downstream of the ΔE-Cop6.
  • Figure 3 OD600 and cell dry weight of ScCop6, ΔE-Cop6, ΔYB-Cop6 and XdCop6 in 10 ml of YPD medium.
  • Figure 4 Chromatograms of the diluted dodecane from (A) X. dendro the hexadecane used as internal standard. The α-cuprenene has a retention
  • Figure 5 Fragmentation patterns. (A) α-cuprenene from ScCop6; (B) peak at 12.8 minutes from XdCop6. The “x” axis represents the m/z ratio.
  • Figure 6 Production of α-cuprenene in rich YPD medium.
  • Figure 7 OD600 and cell dry weight of ScCop6, ΔE-Cop6, ΔYB-Cop6 an
  • Figure 8 Production of α-cuprenene in minimal medium.

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APA

Melillo, E., Setroikromo, R., Quax, W. J., & Kayser, O. (2013). Production of α-cuprenene in Xanthophyllomyces dendrorhous: A step closer to a potent terpene biofactory. Microbial Cell Factories, 12(1). https://doi.org/10.1186/1475-2859-12-13

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