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. 2017 Dec 11;7:17346. doi: 10.1038/s41598-017-17439-2

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© The Author(s) 2017

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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Transcription of mat1-2-1 under different cultivation conditions. qRT-PCR analysis of the relative transcription level of mat1-2-1. The mean values of each column were obtained from three independent biological replicates. Error bars indicated the standard error (SE) from three independent biological replicates. Significant differences (T-test *P < 0.05, **P < 0.01, ***P < 0.001) were detected for the transcription of mat1-2-1 when comparing light and darkness for the indicated inducing carbon sources.