Metabolic engineering of Ashbya gossypii for limonene production from xylose

• Published in: Biotechnology for biofuels Vol. 15; no. 1; pp. 1 - 79
• Main Authors: Muéoz-Fernández, Gloria, Martínez-Buey, Rubén, Revuelta, José Luis, Jiménez, Alberto
• Format: Journal Article
• Language: English
• Published: London BioMed Central Ltd 15-07-2022; BioMed Central; BMC
• Subjects: Agricultural wastes; Analysis; Ashbya gossypii; Biocatalysts; Biodiesel fuels; Biofuels; Biosynthesis; Biotechnological microorganisms; Biotechnology; Carbon; Carbon sources; Citrus limon; Engineering; Enzymes; Evaluation; Food industry; Gene mutations; HMG1 gene; Hydrolysates; Hydroxymethylglutaryl-CoA reductase; Industrial production; Industrial wastes; Lethality; Limonene; Metabolic engineering; Metabolism; Metabolites; Microbial biotechnology; Microorganisms; Mutants; Pesticides; Pharmaceutical industry; Plant extracts; Properties; Proteins; Reductases; Sterols; Terpenes; Xylose; Spain
• ISSN: 2731-3654; 2731-3654; 1754-6834
• DOI: 10.1186/s13068-022-02176-0

Limonene is a cyclic monoterpene that has applications in the food, cosmetic, and pharmaceutical industries. The industrial production of limonene and its derivatives through plant extraction presents important drawbacks such as seasonal and climate issues, feedstock limitations, low efficiency and environmental concerns. Consequently, the implementation of efficient and eco-friendly bioprocesses for the production of limonene and other terpenes constitutes an attractive goal for microbial biotechnology. In this context, novel biocatalysts with the ability to produce limonene from alternative carbon sources will help to meet the industrial demands of limonene. Engineered strains of the industrial fungus Ashbya gossypii have been developed to produce limonene from xylose. The limonene synthase (LS) from Citrus limon was initially overexpressed together with the native HMG1 gene (coding for HMG-CoA reductase) to establish a limonene-producing platform from a xylose-utilizing A. gossypii strain. In addition, several strategies were designed to increase the production of limonene. Hence, the effect of mutant alleles of ERG20 (erg20.sup.F95W and erg20.sup.F126W) were evaluated together with a synthetic orthogonal pathway using a heterologous neryl diphosphate synthase. The lethality of the A. gossypii double mutant erg20.sup.F95W-F126W highlights the indispensability of farnesyl diphosphate for the synthesis of essential sterols. In addition, the utilization of the orthogonal pathway, bypassing the Erg20 activity through neryl diphosphate, triggered a substantial increase in limonene titer (33.6 mg/L), without critically altering the fitness of the engineered strain. Finally, the overexpression of the native ERG12 gene further enhanced limonene production, which reached 336.4 mg/L after 96 h in flask cultures using xylose as the carbon source. The microbial production of limonene can be carried out using engineered strains of A. gossypii from xylose-based carbon sources. The utilization of a synthetic orthogonal pathway together with the overexpression of ERG12 is a highly beneficial strategy for the production of limonene in A. gossypii. The strains presented in this work constitute a proof of principle for the production of limonene and other terpenes from agro-industrial wastes such as xylose-rich hydrolysates in A. gossypii.