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. 2021 Oct 11;11:20116. doi: 10.1038/s41598-021-99490-8

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© The Author(s) 2021

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

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Confocal laser scanning microscopy (CLSM) of the colony boundaries between S. lividans and fungi. Colony boundaries between S. lividans and fungi were observed by CLSM. (A) S. lividans strains were co-cultured with S. pombe (top) and S. cerevisiae (bottom) on a cellophane, and the bottom of the colony boundary was then observed by CLSM. A dotted arrow in the bottom panel indicates the observed region between the colonies. S. lividans and fungi were visualized using Syto59 dye staining (magenta) and GFP expression (green), respectively. Scale bars, 50 μm.