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Altered Lignin Biosynthesis Improves Cellulosic Bioethanol Production in Transgenic Maize Plants Down-Regulated for Cinnamyl Alcohol Dehydrogenase

机译:改变的木质素生物合成改善了肉桂醇脱氢酶下调的转基因玉米植物中纤维素生物乙醇的生产

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摘要

Cinnamyl alcohol dehydrogenase(CAD)is a key enzyme involved in the last step of monolignol biosynthesis.The effect of CAD down-regulation on lignin production was investigated through a transgenic approach in maize.Transgenic CAD-RNAi plants show a different degree of enzymatic reduction depending on the analyzed tissue and show alterations in cell wall composition.Cell walls of CAD-RNAi stems contain a lignin polymer with a slight reduction in the S-to-G ratio without affecting the total lignin content.In addition,these cell walls accumulate higher levels of cellulose and arabinoxylans.In contrast,cell walls of CAD-RNAi midribs present a reduction in the total lignin content and of cell wall polysaccharides.In vitro degradability assays showed that,although to a different extent,the changes induced by the repression of CAD activity produced midribs and stems more degradable than wild-type plants.CAD-RNAi plants grown in the field presented a wild-type phenotype and produced higher amounts of dry biomass.Cellulosic bioethanol assays revealed that CAD-RNAi biomass produced higher levels of ethanol compared to wild-type,making CAD a good target to improve both the nutritional and energetic values of maize lignocellulosic biomass.
机译:肉桂醇脱氢酶(CAD)是参与单木酚生物合成最后一步的关键酶。通过转基因方法研究了玉米下调CAD对木质素产生的影响。转基因CAD-RNAi植物显示出不同程度的酶促还原取决于所分析的组织并显示出细胞壁组成的变化.CAD-RNAi茎的细胞壁包含木质素聚合物,S / G比率略有降低,而不会影响总木质素含量。此外,这些细胞壁会积累相比之下,CAD-RNAi中肋细胞壁的总木质素含量和细胞壁多糖的含量降低。体外降解性试验表明,尽管抑制程度不同,但压抑诱导的变化的CAD活性产生的中肋和茎比野生型植物更易降解。在田间生长的CAD-RNAi植物表现出野生型的表型并产生更高的amo纤维素生物乙醇检测表明,与野生型相比,CAD-RNAi生物质产生的乙醇含量更高,这使CAD成为提高玉米木质纤维素生物质营养价值和能量价值的良好靶标。

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  • 来源
    《分子植物(英文版)》 |2012年第4期|817-830|共14页
  • 作者单位

    Laboratori de Genetica Molecular Vegetal,Centre de Recerca en AgriGenomica(CRAG),Consorci CSIC-IRTA-UAB-UB,Edifici CRAG,Campus UAB,Bellaterra(Cerdanyola del Vallés),08193 Barcelona,Spain;

    Laboratori de Genetica Molecular Vegetal,Centre de Recerca en AgriGenomica(CRAG),Consorci CSIC-IRTA-UAB-UB,Edifici CRAG,Campus UAB,Bellaterra(Cerdanyola del Vallés),08193 Barcelona,Spain;

    Laboratori de Genetica Molecular Vegetal,Centre de Recerca en AgriGenomica(CRAG),Consorci CSIC-IRTA-UAB-UB,Edifici CRAG,Campus UAB,Bellaterra(Cerdanyola del Vallés),08193 Barcelona,Spain;

    Laboratori de Genetica Molecular Vegetal,Centre de Recerca en AgriGenomica(CRAG),Consorci CSIC-IRTA-UAB-UB,Edifici CRAG,Campus UAB,Bellaterra(Cerdanyola del Vallés),08193 Barcelona,Spain;

    Laboratori de Genetica Molecular Vegetal,Centre de Recerca en AgriGenomica(CRAG),Consorci CSIC-IRTA-UAB-UB,Edifici CRAG,Campus UAB,Bellaterra(Cerdanyola del Vallés),08193 Barcelona,Spain;

    (A)rea de Fisiología Vegetal,Universidad de León,24071,Spain;

    Center for Plant Transformation,Iowa State University,G405 Agronomy Hall,Ames,IA 50011-1010,USA;

    Laboratori de Genetica Molecular Vegetal,Centre de Recerca en AgriGenomica(CRAG),Consorci CSIC-IRTA-UAB-UB,Edifici CRAG,Campus UAB,Bellaterra(Cerdanyola del Vallés),08193 Barcelona,Spain;

    Institut Jean-Pierre Bourgin,INRA-AgroParisTech,UMR 1318,78026 Versailles cedex,France;

    Centre de Recherches sur les Macromolecules Végétales-UPR-CNRS-5301,38041 Grenoble Cedex 09,France;

    Centre de Recherches sur les Macromolecules Végétales-UPR-CNRS-5301,38041 Grenoble Cedex 09,France;

    Laboratori de Genetica Molecular Vegetal,Centre de Recerca en AgriGenomica(CRAG),Consorci CSIC-IRTA-UAB-UB,Edifici CRAG,Campus UAB,Bellaterra(Cerdanyola del Vallés),08193 Barcelona,Spain;

  • 收录信息 中国科学引文数据库(CSCD);中国科技论文与引文数据库(CSTPCD);
  • 原文格式 PDF
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