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Metab Eng. 2015 Mar;28:91-103. doi: 10.1016/j.ymben.2014.12.001. Epub 2014 Dec 10.

Reconstructing the chemical diversity of labdane-type diterpene biosynthesis in yeast.

Author information

1
Department of Biochemistry, School of Medicine, University of Crete, P.O. Box 2208, Heraklion 71003, Greece; Mediterranean Agronomic Institute of Chania, P.O. Box 85, Chania 73100, Greece.
2
Department of Pharmacognosy and Chemistry of Natural Products, School of Pharmacy, University of Athens, Panepistimiopolis Zografou, Athens 15771, Greece.
3
Mediterranean Agronomic Institute of Chania, P.O. Box 85, Chania 73100, Greece.
4
Institute of Applied Biosciences-Centre for Research and Technology Hellas (INAB-CERTH), P.O. Box 60361, Thermi, 57001 Thessaloniki, Greece.
5
Institute of Applied Biosciences-Centre for Research and Technology Hellas (INAB-CERTH), P.O. Box 60361, Thermi, 57001 Thessaloniki, Greece; Department of Pharmaceutical Sciences, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece.
6
Department of Biochemistry, School of Medicine, University of Crete, P.O. Box 2208, Heraklion 71003, Greece; Mediterranean Agronomic Institute of Chania, P.O. Box 85, Chania 73100, Greece. Electronic address: s.kampranis@med.uoc.gr.

Abstract

Terpenes are a large class of natural products, many of which are used in cosmetics, pharmaceuticals, or biofuels. However, terpene's industrial application is frequently hindered by limited availability of natural sources or low yields of chemical synthesis. In this report, we developed a modular platform based on standardized and exchangeable parts to reproduce and potentially expand the diversity of terpene structures in Saccharomyces cerevisiae. By combining different module-specific parts, we exploited the substrate promiscuity of class I diterpene synthases to produce an array of labdane-type scaffolds. These were subsequently modified by a scaffold decoration module consisting of a mutant library of a promiscuous cytochrome P450 to afford a range of hydroxylated diterpenes. Further P450 protein engineering yielded dedicated and efficient catalysts for specific products. Terpenes produced include precursors of pharmacologically important compounds, molecules that are difficult to obtain from natural sources, or new natural products. The approach described here provides a platform on which additional gene mining, combinatorial biosynthesis, and protein engineering efforts can be integrated to sustainably explore the terpene chemical space.

KEYWORDS:

Combinatorial biosynthesis; Cytochrome P450; Isoprenoids; Metabolic engineering; Protein engineering

PMID:
25498547
DOI:
10.1016/j.ymben.2014.12.001
[Indexed for MEDLINE]
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