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. 2020 Jul 21;10:12087. doi: 10.1038/s41598-020-68983-3

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© The Author(s) 2020

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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Muralytic activity of Innolysins Ec. Cleared lysates of the Innolysins Ec1-Ec12 (see Fig. 1) were screened for ability to degrade peptidoglycan of P. aeruginosa PAO1 compared to the activity of cleared lysates of cells carrying the empty vector, pVTD (negative control). Phage T5 endolysin (T5 Lys) and receptor binding protein (Pb5) were used as a positive and a negative control, respectively. Average muralytic activities (U/ml cleared lysate) were estimated based on triplicates. *Significant muralytic activity compared to the negative control (cleared lysate of cells carrying the empty vector, pVTD) at P < 0.05.