Abstract
Efficient substrate utilization is the first and most important prerequisite for economically viable production of biofuels and chemicals by microbial cell factories. However, production rates and yields are often compromised by low transport rates of substrates across biological membranes and their diversion to competing pathways. This is especially true when common chassis organisms are engineered to utilize nonphysiological feedstocks. Here, we addressed this problem by constructing an artificial complex between an endogenous sugar transporter and a heterologous xylose isomerase in Saccharomyces cerevisiae. Direct feeding of the enzyme through the transporter resulted in acceleration of xylose consumption and substantially diminished production of xylitol as an undesired side product, with a concomitant increase in the production of ethanol. This underlying principle could also likely be implemented in other biotechnological applications.
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Acknowledgements
Financial support by German Federal Ministry of Food, Agriculture and Consumer Protection following a decision of German Bundestag (to E.B. and M.O.; project ECO-FERM, FKZ: 22031811) is gratefully acknowledged. We would like to thank D. Wolf (University of Stuttgart) for kindly providing Gal2 antibodies. We are grateful to C. Hiesl, C. Hannig and S. Scholl for their contribution to the experimental work. We thank J. Tripp and W. Generoso for stimulating discussions. T. Bionda is acknowledged for critical comments on the manuscript.
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M.O. conceived and supervised the project. E.B. co-supervised the project and provided resources. T.T., I.W., E.B. and M.O. contributed to experimental design. T.T. performed the experiments. T.T. and M.O. analyzed the data. J.C. performed structure modeling. M.O. wrote the manuscript, which was edited and approved by all authors.
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Thomik, T., Wittig, I., Choe, Jy. et al. An artificial transport metabolon facilitates improved substrate utilization in yeast. Nat Chem Biol 13, 1158–1163 (2017). https://doi.org/10.1038/nchembio.2457
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DOI: https://doi.org/10.1038/nchembio.2457
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