Development of a multi-gene expression system in Xanthophyllomyces dendrorhous

• Published in: Microbial cell factories Vol. 13; no. 1; p. 175
• Main Authors: Hara, Kiyotaka Y, Morita, Toshihiko, Mochizuki, Masao, Yamamoto, Keisuke, Ogino, Chiaki, Araki, Michihiro, Kondo, Akihiko
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 04.12.2014; BioMed Central
• Subjects: Analysis; Basidiomycota - genetics; Basidiomycota - metabolism; Beta carotene; Biosynthesis; Cell growth; Cloning; Dehydrogenases; Gene Expression; Genetic aspects; Genetic engineering; Genetically modified organisms; Health aspects; Metabolic Engineering - methods; Metabolism; Microorganisms; Phaffia rhodozyma; Physiological aspects; Plasmids; Protein expression; Ribosomal DNA; Technical Notes; Xanthophyllomyces dendrorhous; Yeasts - genetics; Yeasts - metabolism; Japan
• ISSN: 1475-2859; 1475-2859
• DOI: 10.1186/s12934-014-0175-3

Red yeast, Xanthophyllomyces dendrorhous (Phaffia rhodozyma) is the only yeast known to produce astaxanthin, an anti-oxidant isoprenoid (carotenoid) that is widely used in the aquaculture, food, pharmaceutical and cosmetic industries. Recently, the potential of this microorganism as a platform cell factory for isoprenoid production has been recognized because of high flux through its native terpene pathway. Addition of mevalonate, the common precursor for isoprenoid biosynthesis, has been shown to be critical to enhance the astaxanthin content in X. dendrorhous. However, addition of mevalonate is unrealistic during industrial isoprenoid production because it is an unstable and costly chemical. Therefore, up-regulating the intracellular mevalonate supply by enhancing the mevalonate synthetic pathway though genetic engineering is a promising strategy to improve isoprenoid production in X. dendrorhous. However, a system to strongly express multiple genes has been poorly developed for X. dendrorhous. Here, we developed a multiple gene expression system using plasmids containing three strong promoters in X. dendrorhous (actin, alcohol dehydrogenase and triose-phosphate isomerase) and their terminators. Using this system, three mevalonate synthetic pathway genes encoding acetoacetyl-CoA thiolase, HMG-CoA synthase and HMG-CoA reductase were overexpressed at the same time. This triple overexpressing strain showed an increase in astaxanthin production compared with each single overexpressing strain. Additionally, this triple overexpression of mevalonate synthetic pathway genes together with genes involved in β-carotene and astaxanthin synthesis showed a synergetic effect on increasing astaxanthin production. Finally, astaxanthin production was enhanced by 2.1-fold compared with the parental strain without a reduction of cell growth. We developed a system to strongly overexpress multiple genes in X. dendrorhous. Using this system, the synthetic pathway of mevalonate, a common substrate for isoprenoid biosynthesis, was enhanced, causing an increase in astaxanthin production. Combining this multiple gene overexpression system with a platform strain that overproduces mevalonate has the potential to improve industrial production of various isoprenoids in X. dendrorhous.