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. 2016 Feb 9;15:32. doi: 10.1186/s12934-016-0434-6

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© Rollero et al. 2016

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 5 — Focus on the bioconversion of isoamyl alcohol to isoamyl acetate. a Changes in total isoamyl acetate production as a function of total isoamyl alcohol production in SM330 with 8 mg/L of phytosterols for Lalvin EC1118^® (blue) and Affinity™ ECA5 (red). The arrows indicate the timing of sampling for transcriptomic analyses. b Changes in total isoamyl acetate production as a function of total isoamyl alcohol production subsequently to phytosterol additions for Lalvin EC1118^® (blue) and Affinity™ ECA5 (purple and red). For Lalvin EC1118^®, despite phytosterol additions, bioconversion yield between the two compounds remains identical: 0.0241 (R² = 0.947). For Affinity™ ECA5, four linear phases are identified; their yields of conversion are 0.0689 (R² = 0.990); 0.0367 (R² = 0.966); 0.0696 (R² = 0.991); and 0.0351 (R² = 0.955)