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. 2020 Jul 7;20:198. doi: 10.1186/s12866-020-01876-7

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© The Author(s) 2020

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.

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Fig. 1 — Effect of growth medium on the proportion of 18:2n-6 and its biohydrogenation intermediates (% of total intermediates and 18:2n-6) during a 24 h incubation period with Butyrivibrio fibrisolvens D1 (left; a–d) and Cutibacterium acnes DSM 1897 (right; e–h) (Exp. 3). The initial concentration of 18:2n-6 was 40 μg/mL. Control medium (diamond); low pH medium (square), control medium with pH adjusted to 5.5; DHA-enriched (docosahexaenoic acid) medium (triangle), control medium containing 40 μg/mL of 22:6n-3. c, cis; t, trans; CLA, conjugated linoleic acid