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Molecular breeding of lignin-degrading brown-rot fungus Gloeophyllum trabeum by homologous expression of laccase gene
The basidiomycete Gloeophyllum trabeum KU-41 can degrade Japanese cedar wood efficiently. To construct a strain better suited for biofuel production from Japanese cedar wood, we developed a gene transformation system for G. trabeum KU-41 using the hygromycin phosphotransferase-encoding gene (hpt) as...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4688280/ https://www.ncbi.nlm.nih.gov/pubmed/26695948 http://dx.doi.org/10.1186/s13568-015-0173-9 |
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author | Arimoto, Misa Yamagishi, Kenji Wang, Jianqiao Tanaka, Kanade Miyoshi, Takanori Kamei, Ichiro Kondo, Ryuichiro Mori, Toshio Kawagishi, Hirokazu Hirai, Hirofumi |
author_facet | Arimoto, Misa Yamagishi, Kenji Wang, Jianqiao Tanaka, Kanade Miyoshi, Takanori Kamei, Ichiro Kondo, Ryuichiro Mori, Toshio Kawagishi, Hirokazu Hirai, Hirofumi |
author_sort | Arimoto, Misa |
collection | PubMed |
description | The basidiomycete Gloeophyllum trabeum KU-41 can degrade Japanese cedar wood efficiently. To construct a strain better suited for biofuel production from Japanese cedar wood, we developed a gene transformation system for G. trabeum KU-41 using the hygromycin phosphotransferase-encoding gene (hpt) as a marker. The endogenous laccase candidate gene (Gtlcc3) was fused with the promoter of the G. trabeum glyceraldehyde-3-phosphate dehydrogenase-encoding gene and co-transformed with the hpt-bearing pAH marker plasmid. We obtained 44 co-transformants, and identified co-transformant L#61, which showed the highest laccase activity among all the transformants. Moreover, strain L#61 was able to degrade lignin in Japanese cedar wood-containing medium, in contrast to wild-type G. trabeum KU-41 and to a typical white-rot fungus Phanerochaete chrysosporium. By using strain L#61, direct ethanol production from Japanese cedar wood was improved compared to wild type. To our knowledge, this study is the first report of the molecular breeding of lignin-degrading brown-rot fungus and direct ethanol production from softwoods by co-transformation with laccase overproduction constructs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13568-015-0173-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4688280 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-46882802015-12-23 Molecular breeding of lignin-degrading brown-rot fungus Gloeophyllum trabeum by homologous expression of laccase gene Arimoto, Misa Yamagishi, Kenji Wang, Jianqiao Tanaka, Kanade Miyoshi, Takanori Kamei, Ichiro Kondo, Ryuichiro Mori, Toshio Kawagishi, Hirokazu Hirai, Hirofumi AMB Express Original Article The basidiomycete Gloeophyllum trabeum KU-41 can degrade Japanese cedar wood efficiently. To construct a strain better suited for biofuel production from Japanese cedar wood, we developed a gene transformation system for G. trabeum KU-41 using the hygromycin phosphotransferase-encoding gene (hpt) as a marker. The endogenous laccase candidate gene (Gtlcc3) was fused with the promoter of the G. trabeum glyceraldehyde-3-phosphate dehydrogenase-encoding gene and co-transformed with the hpt-bearing pAH marker plasmid. We obtained 44 co-transformants, and identified co-transformant L#61, which showed the highest laccase activity among all the transformants. Moreover, strain L#61 was able to degrade lignin in Japanese cedar wood-containing medium, in contrast to wild-type G. trabeum KU-41 and to a typical white-rot fungus Phanerochaete chrysosporium. By using strain L#61, direct ethanol production from Japanese cedar wood was improved compared to wild type. To our knowledge, this study is the first report of the molecular breeding of lignin-degrading brown-rot fungus and direct ethanol production from softwoods by co-transformation with laccase overproduction constructs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13568-015-0173-9) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2015-12-22 /pmc/articles/PMC4688280/ /pubmed/26695948 http://dx.doi.org/10.1186/s13568-015-0173-9 Text en © Arimoto et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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. |
spellingShingle | Original Article Arimoto, Misa Yamagishi, Kenji Wang, Jianqiao Tanaka, Kanade Miyoshi, Takanori Kamei, Ichiro Kondo, Ryuichiro Mori, Toshio Kawagishi, Hirokazu Hirai, Hirofumi Molecular breeding of lignin-degrading brown-rot fungus Gloeophyllum trabeum by homologous expression of laccase gene |
title | Molecular breeding of lignin-degrading brown-rot fungus Gloeophyllum trabeum by homologous expression of laccase gene |
title_full | Molecular breeding of lignin-degrading brown-rot fungus Gloeophyllum trabeum by homologous expression of laccase gene |
title_fullStr | Molecular breeding of lignin-degrading brown-rot fungus Gloeophyllum trabeum by homologous expression of laccase gene |
title_full_unstemmed | Molecular breeding of lignin-degrading brown-rot fungus Gloeophyllum trabeum by homologous expression of laccase gene |
title_short | Molecular breeding of lignin-degrading brown-rot fungus Gloeophyllum trabeum by homologous expression of laccase gene |
title_sort | molecular breeding of lignin-degrading brown-rot fungus gloeophyllum trabeum by homologous expression of laccase gene |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4688280/ https://www.ncbi.nlm.nih.gov/pubmed/26695948 http://dx.doi.org/10.1186/s13568-015-0173-9 |
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