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Mnsod1 promotes the development of Pleurotus ostreatus and enhances the tolerance of mycelia to heat stress

BACKGROUND: Superoxide dismutases (SODs, EC 1.15.1.1) are defense proteins that can be used as sweepers to clear reactive oxygen species (ROS). They have been widely studied in the plant. Intensive research demonstrates that SOD plays an essential role in plants. However, in Pleurotus ostreatus, the...

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Autores principales: Hou, Ludan, Liu, Zongqi, Yan, Kexing, Xu, Lijing, Chang, Mingchang, Meng, Junlong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9358896/
https://www.ncbi.nlm.nih.gov/pubmed/35934720
http://dx.doi.org/10.1186/s12934-022-01878-2
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author Hou, Ludan
Liu, Zongqi
Yan, Kexing
Xu, Lijing
Chang, Mingchang
Meng, Junlong
author_facet Hou, Ludan
Liu, Zongqi
Yan, Kexing
Xu, Lijing
Chang, Mingchang
Meng, Junlong
author_sort Hou, Ludan
collection PubMed
description BACKGROUND: Superoxide dismutases (SODs, EC 1.15.1.1) are defense proteins that can be used as sweepers to clear reactive oxygen species (ROS). They have been widely studied in the plant. Intensive research demonstrates that SOD plays an essential role in plants. However, in Pleurotus ostreatus, the function and regulatory pathway of SOD in the growth and development and the abiotic stress response have not been clear. RESULTS: In this study, three MnSOD-encoding genes of the P. ostreatus CCMSSC00389 strain were cloned and identified. Mnsod1, Mnsod2, and Mnsod3 were interrupted by 3, 7, and 2 introns, and encoded proteins of 204, 220, and 344 amino acids, respectively. By comparing the relative expression of three MnSOD-encoding genes in mycelia, the results showed that the gene with the highest primary expression was Mnsod1. Subsequently, the function of P. ostreatus Mnsod1 was explored by overexpression (OE) and RNA interference (RNAi). The results showed that during the growth and development of P. ostreatus, MnSOD1 protein increased gradually from mycelia to the fruiting body, but decreased in spores. The change of Mnsod1 transcription level was not consistent with the changing trend of MnSOD1 protein. Further studies showed that during primordia formation, the expression of Mnsod1 gradually increased, reaching a peak at 48 h, and the transcription level was 2.05-folds compared to control. H(2)O(2) content progressively accumulated during the formation of primordia, and its change trend was similar to that of Mnsod1 transcription. OE-Mnsod1-1 and OE-Mnsod1-21 strains accelerated the formation of primordia. The results suggested that Mnsod1 may participate in the formation rate of P. ostreatus primordium by regulating the signal molecule H(2)O(2). In addition, OE-Mnsod1-1 and OE-Mnsod1-21 strains shortened the mycelial recovery time after heat stress and improved the tolerance of the strains to 2.5 mM and 5 mM H(2)O(2), which showed that Mnsod1 was involved in the response of P. ostreatus mycelium to heat stress. CONCLUSIONS: This study indicates that Mnsod1 plays an active role in the formation of P. ostreatus primordia and the response to abiotic stress. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12934-022-01878-2.
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spelling pubmed-93588962022-08-10 Mnsod1 promotes the development of Pleurotus ostreatus and enhances the tolerance of mycelia to heat stress Hou, Ludan Liu, Zongqi Yan, Kexing Xu, Lijing Chang, Mingchang Meng, Junlong Microb Cell Fact Research BACKGROUND: Superoxide dismutases (SODs, EC 1.15.1.1) are defense proteins that can be used as sweepers to clear reactive oxygen species (ROS). They have been widely studied in the plant. Intensive research demonstrates that SOD plays an essential role in plants. However, in Pleurotus ostreatus, the function and regulatory pathway of SOD in the growth and development and the abiotic stress response have not been clear. RESULTS: In this study, three MnSOD-encoding genes of the P. ostreatus CCMSSC00389 strain were cloned and identified. Mnsod1, Mnsod2, and Mnsod3 were interrupted by 3, 7, and 2 introns, and encoded proteins of 204, 220, and 344 amino acids, respectively. By comparing the relative expression of three MnSOD-encoding genes in mycelia, the results showed that the gene with the highest primary expression was Mnsod1. Subsequently, the function of P. ostreatus Mnsod1 was explored by overexpression (OE) and RNA interference (RNAi). The results showed that during the growth and development of P. ostreatus, MnSOD1 protein increased gradually from mycelia to the fruiting body, but decreased in spores. The change of Mnsod1 transcription level was not consistent with the changing trend of MnSOD1 protein. Further studies showed that during primordia formation, the expression of Mnsod1 gradually increased, reaching a peak at 48 h, and the transcription level was 2.05-folds compared to control. H(2)O(2) content progressively accumulated during the formation of primordia, and its change trend was similar to that of Mnsod1 transcription. OE-Mnsod1-1 and OE-Mnsod1-21 strains accelerated the formation of primordia. The results suggested that Mnsod1 may participate in the formation rate of P. ostreatus primordium by regulating the signal molecule H(2)O(2). In addition, OE-Mnsod1-1 and OE-Mnsod1-21 strains shortened the mycelial recovery time after heat stress and improved the tolerance of the strains to 2.5 mM and 5 mM H(2)O(2), which showed that Mnsod1 was involved in the response of P. ostreatus mycelium to heat stress. CONCLUSIONS: This study indicates that Mnsod1 plays an active role in the formation of P. ostreatus primordia and the response to abiotic stress. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12934-022-01878-2. BioMed Central 2022-08-08 /pmc/articles/PMC9358896/ /pubmed/35934720 http://dx.doi.org/10.1186/s12934-022-01878-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Hou, Ludan
Liu, Zongqi
Yan, Kexing
Xu, Lijing
Chang, Mingchang
Meng, Junlong
Mnsod1 promotes the development of Pleurotus ostreatus and enhances the tolerance of mycelia to heat stress
title Mnsod1 promotes the development of Pleurotus ostreatus and enhances the tolerance of mycelia to heat stress
title_full Mnsod1 promotes the development of Pleurotus ostreatus and enhances the tolerance of mycelia to heat stress
title_fullStr Mnsod1 promotes the development of Pleurotus ostreatus and enhances the tolerance of mycelia to heat stress
title_full_unstemmed Mnsod1 promotes the development of Pleurotus ostreatus and enhances the tolerance of mycelia to heat stress
title_short Mnsod1 promotes the development of Pleurotus ostreatus and enhances the tolerance of mycelia to heat stress
title_sort mnsod1 promotes the development of pleurotus ostreatus and enhances the tolerance of mycelia to heat stress
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9358896/
https://www.ncbi.nlm.nih.gov/pubmed/35934720
http://dx.doi.org/10.1186/s12934-022-01878-2
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