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. 2017 Jun 2;7:2715. doi: 10.1038/s41598-017-02996-3

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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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Representative 2-D gels of cellular proteins of S. pneumoniae TIGR4 (A and B) and R6 (C and D) cultured without (A and C) and with 0.5 × MIC purified rhodomyrtone (B and D). The isolated proteins were separated by isoelectric focusing in the pI range of 4 to 7 in the first dimension (11 cm). The proteins were further separated by 10% SDS-PAGE in the second dimension. Spot numbers indicate spots with altered abundances: those marked in (A and C) diminished after rhodomyrtone treatment, and those marked in (B and D) augmented after rhodomyrtone exposure.