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Silencing of a BAHD acyltransferase in sugarcane increases biomass digestibility

BACKGROUND: Sugarcane (Saccharum spp.) covers vast areas of land (around 25 million ha worldwide), and its processing is already linked into infrastructure for producing bioethanol in many countries. This makes it an ideal candidate for improving composition of its residues (mostly cell walls), maki...

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Detalles Bibliográficos
Autores principales: de Souza, Wagner Rodrigo, Pacheco, Thályta Fraga, Duarte, Karoline Estefani, Sampaio, Bruno Leite, de Oliveira Molinari, Patrícia Abrão, Martins, Polyana Kelly, Santiago, Thaís Ribeiro, Formighieri, Eduardo Fernandes, Vinecky, Felipe, Ribeiro, Ana Paula, da Cunha, Bárbara Andrade Dias Brito, Kobayashi, Adilson Kenji, Mitchell, Rowan Andrew Craig, de Sousa Rodrigues Gambetta, Dasciana, Molinari, Hugo Bruno Correa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6501328/
https://www.ncbi.nlm.nih.gov/pubmed/31080518
http://dx.doi.org/10.1186/s13068-019-1450-7
Descripción
Sumario:BACKGROUND: Sugarcane (Saccharum spp.) covers vast areas of land (around 25 million ha worldwide), and its processing is already linked into infrastructure for producing bioethanol in many countries. This makes it an ideal candidate for improving composition of its residues (mostly cell walls), making them more suitable for cellulosic ethanol production. In this paper, we report an approach to improving saccharification of sugarcane straw by RNAi silencing of the recently discovered BAHD01 gene responsible for feruloylation of grass cell walls. RESULTS: We identified six BAHD genes in the sugarcane genome (SacBAHDs) and generated five lines with substantially decreased SacBAHD01 expression. To find optimal conditions for determining saccharification of sugarcane straw, we tried multiple combinations of solvent and temperature pretreatment conditions, devising a predictive model for finding their effects on glucose release. Under optimal conditions, demonstrated by Organosolv pretreatment using 30% ethanol for 240 min, transgenic lines showed increases in saccharification efficiency of up to 24%. The three lines with improved saccharification efficiency had lower cell-wall ferulate content but unchanged monosaccharide and lignin compositions. CONCLUSIONS: The silencing of SacBAHD01 gene and subsequent decrease of cell-wall ferulate contents indicate a promising novel biotechnological approach for improving the suitability of sugarcane residues for cellulosic ethanol production. In addition, the Organosolv pretreatment of the genetically modified biomass and the optimal conditions for the enzymatic hydrolysis presented here might be incorporated in the sugarcane industry for bioethanol production. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-019-1450-7) contains supplementary material, which is available to authorized users.