Overexpression of the Squalene Epoxidase Gene Alone and in Combination with the 3‑Hydroxy-3-methylglutaryl Coenzyme A Gene Increases Ganoderic Acid Production in Ganoderma lingzhi

• Published in: Journal of agricultural and food chemistry 2017-06, Vol.65 (23), p.4683-4690
• Main Authors: Zhang, De-Huai, Jiang, Lu-Xi, Li, Na, Yu, Xuya, Zhao, Peng, Li, Tao, Xu, Jun-Wei
• Format: Article
• Language: English
• Subjects: Acyl Coenzyme A - genetics; Acyl Coenzyme A - metabolism; Biosynthetic Pathways; Fungal Proteins - genetics; Fungal Proteins - metabolism; Ganoderma - enzymology; Ganoderma - genetics; Ganoderma - metabolism; Gene Expression; Squalene Monooxygenase - genetics; Squalene Monooxygenase - metabolism; Triterpenes - metabolism
• ISSN: 0021-8561; 1520-5118
• DOI: 10.1021/acs.jafc.7b00629

The squalene epoxidase (SE) gene from the biosynthetic pathway of ganoderic acid (GA) was cloned and overexpressed in Ganoderma lingzhi. The strain that overexpressed the SE produced approximately 2 times more GA molecules than the wild-type (WT) strain. Moreover, SE overexpression upregulated lanosterol synthase gene expression in the biosynthetic pathway. These results indicated that SE stimulates GA accumulation. Then, the SE and 3-hydroxy-3-methylglutaryl coenzyme A (HMGR) genes were simultaneously overexpressed in G. lingzhi. Compared with the individual overexpression of SE or HMGR, the combined overexpression of the two genes further enhanced individual GA production. The overexpressing strain produced maximum GA-T, GA-S, GA-Mk, and GA-Me contents of 90.4 ± 7.5, 35.9 ± 5.4, 6.2 ± 0.5, and 61.8 ± 5.8 μg/100 mg dry weight, respectively. These values were 5.9, 4.5, 2.4, and 5.8 times higher than those produced by the WT strain. This is the first example of the successful manipulation of multiple biosynthetic genes to improve GA content in G. lingzhi.