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. 2020 Aug 31;10:14325. doi: 10.1038/s41598-020-71297-z

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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 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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Immunodetection of EnaA-GFP and EnaB-GFP. Western-blot analyses showing patterns of EnaA and EnaB bands in total protein extracts of mycelia cultured in the absence (C) and presence of 1 M NaCl, 0.3 M LiCl or alkaline pH for (A) 1 h and (B) 5 h. GFP-tagged fusion were subjected to immunodetection using α-GFP primary antibody. The expected full-length chimeras are indicated with an arrow and the detected modified forms are indicated with a bracket. Actin was used as loading control.