dc.contributor.author | López Malvar, Ana | |
dc.contributor.author | Malvar, Rosa Ana | |
dc.contributor.author | Souto, Xose Carlos | |
dc.contributor.author | Gómez, Leonardo Dario | |
dc.contributor.author | Simister, Rachael | |
dc.contributor.author | Encina, Antonio | |
dc.contributor.author | Barros Rios, Jaime | |
dc.contributor.author | Pereira Crespo, Sonia | |
dc.contributor.author | Santiago Carabelos, Rogelio | |
dc.date.accessioned | 2021-11-25T13:40:58Z | |
dc.date.available | 2021-11-25T13:40:58Z | |
dc.date.issued | 2021-06-02 | |
dc.identifier.citation | BMC Plant Biology, 21(1): 251 (2021) | spa |
dc.identifier.issn | 14712229 | |
dc.identifier.uri | http://hdl.handle.net/11093/2760 | |
dc.description.abstract | Background
Besides the use of maize grain as food and feed, maize stover can be a profitable by-product for cellulosic ethanol production, whereas the whole plant can be used for silage production. However, yield is reduced by pest damages, stem corn borers being one of the most important yield constraints. Overall, cell wall composition is key in determining the quality of maize biomass, as well as pest resistance. This study aims to evaluate the composition of the four cell wall fractions (cellulose, hemicellulose, lignin and hydroxycinnamates) in diverse maize genotypes and to understand how this composition influences the resistance to pests, ethanol capacity and digestibility.
Results
The following results can be highlighted: (i) pests’ resistant materials may show cell walls with low p-coumaric acid and low hemicellulose content; (ii) inbred lines showing cell walls with high cellulose content and high diferulate cross-linking may present higher performance for ethanol production; (iii) and inbreds with enhanced digestibility may have cell walls poor in neutral detergent fibre and diferulates, combined with a lignin polymer composition richer in G subunits.
Conclusions
Results evidence that there is no maize cell wall ideotype among the tested for optimal performance for various uses, and maize plants should be specifically bred for each particular application | eng |
dc.description.sponsorship | Agencia Estatal de Investigación | Ref. RTI2018–096776-B-C21 | spa |
dc.description.sponsorship | Agencia Estatal de Investigación | Ref. RTI2018–096776-B-C22 | spa |
dc.language.iso | eng | spa |
dc.publisher | BMC Plant Biology | spa |
dc.relation | info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/RTI2018-096776-B-C21/ES | |
dc.relation | info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/RTI2018-096776-B-C22/ES | |
dc.rights | Attribution 4.0 International | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.title | Elucidating the multifunctional role of the cell wall components in the maize exploitation | eng |
dc.type | article | spa |
dc.rights.accessRights | openAccess | spa |
dc.identifier.doi | 10.1186/s12870-021-03040-3 | |
dc.identifier.editor | https://bmcplantbiol.biomedcentral.com/articles/10.1186/s12870-021-03040-3 | spa |
dc.publisher.departamento | Bioloxía vexetal e ciencias do solo | spa |
dc.publisher.grupoinvestigacion | Agrobioloxía Ambiental: Calidade, Solos e Plantas | spa |
dc.subject.unesco | 3103.01 Producción de Cultivos | spa |
dc.subject.unesco | 3103.08 Gestión de la Producción Vegetal | spa |
dc.subject.unesco | 2417 Biología Vegetal (Botánica) | spa |
dc.date.updated | 2021-11-25T09:23:28Z | |
dc.computerCitation | pub_title=BMC Plant Biology|volume=21|journal_number=1|start_pag=251|end_pag= | spa |
dc.references | We are grateful to Prof. Simon J McQueen Mason for their support at the CNAP, University of York, UK. We thank Lana Reid for the transfer of the Canadian inbred lines, and the Dixon laboratory at University of North Texas for support with the lignin compositional analyses. We thank Dr. Pedro Revilla and Dr. Ana Butrón for the final proof read of the manuscript | spa |