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. 2018 Sep 11;8:13576. doi: 10.1038/s41598-018-31851-2

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© The Author(s) 2018

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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In vivo interaction of the proteins using bacterial two-hybrid system. Coding sequences of the studied genes were cloned in bacterial two-hybrid plasmids pT18 and pT25. Recombinants plasmids were introduced in E. coli BTH101 in different combinations as indicated on the graph. β-galactosidase activity was assayed on cells grown overnight in the presence of IPTG and was expressed in arbitrary units⁶².