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Characterization of Novel Sorghum brown midrib Mutants from an EMS-Mutagenized Population
Reducing lignin concentration in lignocellulosic biomass can increase forage digestibility for ruminant livestock and saccharification yields of biomass for bioenergy. In sorghum (Sorghum bicolor (L.) Moench) and several other C4 grasses, brown midrib (bmr) mutants have been shown to reduce lignin c...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Genetics Society of America
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4232537/ https://www.ncbi.nlm.nih.gov/pubmed/25187038 http://dx.doi.org/10.1534/g3.114.014001 |
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author | Sattler, Scott E. Saballos, Ana Xin, Zhanguo Funnell-Harris, Deanna L. Vermerris, Wilfred Pedersen, Jeffrey F. |
author_facet | Sattler, Scott E. Saballos, Ana Xin, Zhanguo Funnell-Harris, Deanna L. Vermerris, Wilfred Pedersen, Jeffrey F. |
author_sort | Sattler, Scott E. |
collection | PubMed |
description | Reducing lignin concentration in lignocellulosic biomass can increase forage digestibility for ruminant livestock and saccharification yields of biomass for bioenergy. In sorghum (Sorghum bicolor (L.) Moench) and several other C4 grasses, brown midrib (bmr) mutants have been shown to reduce lignin concentration. Putative bmr mutants isolated from an EMS-mutagenized population were characterized and classified based on their leaf midrib phenotype and allelism tests with the previously described sorghum bmr mutants bmr2, bmr6, and bmr12. These tests resulted in the identification of additional alleles of bmr2, bmr6, and bmr12, and, in addition, six bmr mutants were identified that were not allelic to these previously described loci. Further allelism testing among these six bmr mutants showed that they represented four novel bmr loci. Based on this study, the number of bmr loci uncovered in sorghum has doubled. The impact of these lines on agronomic traits and lignocellulosic composition was assessed in a 2-yr field study. Overall, most of the identified bmr lines showed reduced lignin concentration of their biomass relative to wild-type (WT). Effects of the six new bmr mutants on enzymatic saccharification of lignocellulosic materials were determined, but the amount of glucose released from the stover was similar to WT in all cases. Like bmr2, bmr6, and bmr12, these mutants may affect monolignol biosynthesis and may be useful for bioenergy and forage improvement when stacked together or in combination with the three previously described bmr alleles. |
format | Online Article Text |
id | pubmed-4232537 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Genetics Society of America |
record_format | MEDLINE/PubMed |
spelling | pubmed-42325372014-11-18 Characterization of Novel Sorghum brown midrib Mutants from an EMS-Mutagenized Population Sattler, Scott E. Saballos, Ana Xin, Zhanguo Funnell-Harris, Deanna L. Vermerris, Wilfred Pedersen, Jeffrey F. G3 (Bethesda) Investigations Reducing lignin concentration in lignocellulosic biomass can increase forage digestibility for ruminant livestock and saccharification yields of biomass for bioenergy. In sorghum (Sorghum bicolor (L.) Moench) and several other C4 grasses, brown midrib (bmr) mutants have been shown to reduce lignin concentration. Putative bmr mutants isolated from an EMS-mutagenized population were characterized and classified based on their leaf midrib phenotype and allelism tests with the previously described sorghum bmr mutants bmr2, bmr6, and bmr12. These tests resulted in the identification of additional alleles of bmr2, bmr6, and bmr12, and, in addition, six bmr mutants were identified that were not allelic to these previously described loci. Further allelism testing among these six bmr mutants showed that they represented four novel bmr loci. Based on this study, the number of bmr loci uncovered in sorghum has doubled. The impact of these lines on agronomic traits and lignocellulosic composition was assessed in a 2-yr field study. Overall, most of the identified bmr lines showed reduced lignin concentration of their biomass relative to wild-type (WT). Effects of the six new bmr mutants on enzymatic saccharification of lignocellulosic materials were determined, but the amount of glucose released from the stover was similar to WT in all cases. Like bmr2, bmr6, and bmr12, these mutants may affect monolignol biosynthesis and may be useful for bioenergy and forage improvement when stacked together or in combination with the three previously described bmr alleles. Genetics Society of America 2014-09-02 /pmc/articles/PMC4232537/ /pubmed/25187038 http://dx.doi.org/10.1534/g3.114.014001 Text en Copyright © 2014 Sattler et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Unported License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Investigations Sattler, Scott E. Saballos, Ana Xin, Zhanguo Funnell-Harris, Deanna L. Vermerris, Wilfred Pedersen, Jeffrey F. Characterization of Novel Sorghum brown midrib Mutants from an EMS-Mutagenized Population |
title | Characterization of Novel Sorghum brown midrib Mutants from an EMS-Mutagenized Population |
title_full | Characterization of Novel Sorghum brown midrib Mutants from an EMS-Mutagenized Population |
title_fullStr | Characterization of Novel Sorghum brown midrib Mutants from an EMS-Mutagenized Population |
title_full_unstemmed | Characterization of Novel Sorghum brown midrib Mutants from an EMS-Mutagenized Population |
title_short | Characterization of Novel Sorghum brown midrib Mutants from an EMS-Mutagenized Population |
title_sort | characterization of novel sorghum brown midrib mutants from an ems-mutagenized population |
topic | Investigations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4232537/ https://www.ncbi.nlm.nih.gov/pubmed/25187038 http://dx.doi.org/10.1534/g3.114.014001 |
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