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Public Library of Science, PLoS ONE, 12(7), p. e52498, 2012

DOI: 10.1371/journal.pone.0052498

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Reconstruction and Evaluation of the Synthetic Bacterial MEP Pathway in Saccharomyces cerevisiae

Journal article published in 2012 by Siavash Partow, Verena Siewers, Laurent Daviet, Michel Schalk, Jens B. Nielsen
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

Isoprenoids, which are a large group of natural and chemical compounds with a variety of applications as e.g. fragrances, pharmaceuticals and potential biofuels, are produced via two different metabolic pathways, the mevalonate (MVA) pathway and the 2-C-methyl-D-erythritol 4-phosphate (MEP) pathway. Here, we attempted to replace the endogenous MVA pathway in Saccharomyces cerevisiae by a synthetic bacterial MEP pathway integrated into the genome to benefit from its superior properties in terms of energy consumption and productivity at defined growth conditions. It was shown that the growth of a MVA pathway deficient S. cerevisiae strain could not be restored by the heterologous MEP pathway even when accompanied by the co-expression of genes erpA, hISCA1 and CpIscA involved in the Fe-S trafficking routes leading to maturation of IspG and IspH and E. coli genes fldA and fpr encoding flavodoxin and flavodoxin reductase believed to be responsible for electron transfer to IspG and IspH. Citation: Partow S, Siewers V, Daviet L, Schalk M, Nielsen J (2012) Reconstruction and Evaluation of the Synthetic Bacterial MEP Pathway in Saccharomyces cerevisiae. PLoS ONE 7(12): e52498. doi:10.1371/journal.pone.0052498 Copyright: ß 2012 Partow et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Funding: The Knut and Alice Wallenberg Foundation, the Chalmers Foundation and Firmenich AG have financially supported this work. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Competing Interests: The authors have the following competing interests. Authors L.D. and M.S. declare an interest in FIRMENICH SA as employees of the R&D division. FIRMENICH SA is engaged in the production and commercialization of high-value natural and synthetic ingredients for the flavor and fragrance industry. There are no patents, products in development or marketed products to declare. This does not alter the authors' adherence to all the PLOS ONE policies on sharing data and materials.