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Biotechnol Biofuels. 2017 Oct 23;10:241. doi: 10.1186/s13068-017-0927-5. eCollection 2017.

Rhodosporidium toruloides: a new platform organism for conversion of lignocellulose into terpene biofuels and bioproducts.

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Joint BioEnergy Institute, 5885 Hollis St, Emeryville, CA 94608 USA.
Pacific Northwest National Laboratory, 902 Battelle Blvd, Richland, WA 99354 USA.
California Institute of Quantitative Biosciences (QB3), University of California, Berkeley, Berkeley, CA 94720 USA.
Energy Biosciences Institute, 2151 Berkeley Way, Berkeley, CA 94704 USA.
Department of Biomass Science and Conversion Technology, Sandia National Laboratories, Livermore, CA 94551 USA.
Lawrence Berkeley National Laboratory, 1 Cyclotron Rd, Berkeley, CA 94720 USA.
Department of Chemical & Biomolecular Engineering, University of California, Berkeley, Berkeley, CA 94720 USA.
Department of Bioengineering, University of California, Berkeley, Berkeley, CA 94720 USA.



Economical conversion of lignocellulosic biomass into biofuels and bioproducts is central to the establishment of a robust bioeconomy. This requires a conversion host that is able to both efficiently assimilate the major lignocellulose-derived carbon sources and divert their metabolites toward specific bioproducts.


In this study, the carotenogenic yeast Rhodosporidium toruloides was examined for its ability to convert lignocellulose into two non-native sesquiterpenes with biofuel (bisabolene) and pharmaceutical (amorphadiene) applications. We found that R. toruloides can efficiently convert a mixture of glucose and xylose from hydrolyzed lignocellulose into these bioproducts, and unlike many conventional production hosts, its growth and productivity were enhanced in lignocellulosic hydrolysates relative to purified substrates. This organism was demonstrated to have superior growth in corn stover hydrolysates prepared by two different pretreatment methods, one using a novel biocompatible ionic liquid (IL) choline α-ketoglutarate, which produced 261 mg/L of bisabolene at bench scale, and the other using an alkaline pretreatment, which produced 680 mg/L of bisabolene in a high-gravity fed-batch bioreactor. Interestingly, R. toruloides was also observed to assimilate p-coumaric acid liberated from acylated grass lignin in the IL hydrolysate, a finding we verified with purified substrates. R. toruloides was also able to consume several additional compounds with aromatic motifs similar to lignin monomers, suggesting that this organism may have the metabolic potential to convert depolymerized lignin streams alongside lignocellulosic sugars.


This study highlights the natural compatibility of R. toruloides with bioprocess conditions relevant to lignocellulosic biorefineries and demonstrates its ability to produce non-native terpenes.


Amorphadiene; Bisabolene; Heterologous expression; Multiple carbon source utilization; Plant biomass-derived hydrolysate; Rhodosporidium toruloides; Terpenes

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