Biotechnological Production of Statins: Metabolic Aspects and Genetic Approaches

Curr Pharm Biotechnol. 2019;20(15):1244-1259. doi: 10.2174/1389201020666190718165746.

Abstract

Statins are drugs used for people with abnormal lipid levels (hyperlipidemia) and are among the best-selling medications in the United States. Thus, the aspects related to the production of these drugs are of extreme importance for the pharmaceutical industry. Herein, we provide a non-exhaustive review of fungal species used to produce statin and highlighted the major factors affecting the efficacy of this process. The current biotechnological approaches and the advances of a metabolic engineer to improve statins production are also emphasized. The biotechnological production of the main statins (lovastatin, pravastatin and simvastatin) uses different species of filamentous fungi, for example Aspergillus terreus. The statins production is influenced by different types of nutrients available in the medium such as the carbon and nitrogen sources, and several researches have focused their efforts to find the optimal cultivation conditions. Enzymes belonging to Lov class, play essential roles in statin production and have been targeted to genetic manipulations in order to improve the efficiency for Lovastatin and Simvastatin production. For instance, Escherichia coli strains expressing the LovD have been successfully used for lovastatin production. Other examples include the use of iRNA targeting LovF of A. terreus. Therefore, fungi are important allies in the fight against hyperlipidemias. Although many studies have been conducted, investigations on bioprocess optimization (using both native or genetic- modified strains) still necessary.

Keywords: Hyperlipidemia; fermentation processes; genetic manipulation; heterologous expression; microbial secondary metabolites; polyketides..

Publication types

  • Review

MeSH terms

  • Animals
  • Biotechnology / methods*
  • Fermentation
  • Fungi / genetics
  • Fungi / metabolism*
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / pharmacology*
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / toxicity
  • Hyperlipidemias / drug therapy
  • Lovastatin / biosynthesis*
  • Lovastatin / pharmacology
  • Lovastatin / toxicity
  • Metabolic Engineering / methods*
  • Pravastatin / biosynthesis*
  • Pravastatin / pharmacology
  • Pravastatin / toxicity

Substances

  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Lovastatin
  • Pravastatin