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. 2019 Feb 1;6:24. doi: 10.1038/s41438-018-0104-4

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© The Author(s) 2019

Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 7 — a The benzyl alcohol acetyltransferase activity of PmBEAT34, PmBEAT36 and PmBEAT37. The PmBEAT genes were expressed in tobacco leaves by Agrobacterium injection, and the crude protein was extracted for enzyme activity analysis. The data are presented as the mean values of three replicates ± SD. **P < 0.01 (Student’s t-test). Three independent experiments were performed with similar results. b Detection of the expression levels of PmBEAT34, PmBEAT36 and PmBEAT37 in tobacco leaves by sq-RT-PCR. NbTubulin was used as the reference gene. c Confocal images of petal protoplasts expressing PmBEAT proteins containing the GFP tag. The scale bars are 20 μM