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Functional Characterization of a Glycosyltransferase from the Moss Physcomitrella patens Involved in the Biosynthesis of a Novel Cell Wall Arabinoglucan

机译:糖基转移酶的功能表征来自苔藓Physcomitrella含量的含有新型细胞壁的生物合成的葡萄球菌

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摘要

Mixed-linkage (1,3; 1,4)-beta-glucan (MLG), an abundant cell wall polysaccharide in the Poaceae, has been detected in ascomycetes, algae, and seedless vascular plants, but not in eudicots. Although MLG has not been reported in bryophytes, a predicted glycosyltransferase from the moss Physcomitrella patens (Pp3c12_24670) is similar to a bona fide ascomycete MLG synthase. We tested whether Pp3c12_24670 encodes an MLG synthase by expressing it in wild tobacco (Nicotiana benthamiana) and testing for release of diagnostic oligosaccharides from the cell walls by either lichenase or (1,4)-beta-glucan endohydrolase. Lichenase, an MLG-specific endohydrolase, showed no activity against cell walls from transformed N. benthamiana, but (1,4)-beta-glucan endohydrolase released oligosaccharides that were distinct from oligosaccharides released from MLG by this enzyme. Further analysis revealed that these oligosaccharides were derived from a novel unbranched, unsubstituted arabinoglucan (AGlc) polysaccharide. We identified sequences similar to the P. patens AGlc synthase from algae, bryophytes, lycophytes, and monilophytes, raising the possibility that other early divergent plants synthesize AGlc. Similarity of P. patens AGlc synthase to MLG synthases from ascomycetes, but not those from Poaceae, suggests that AGlc and MLG have a common evolutionary history that includes loss in seed plants, followed by a more recent independent origin of MLG within the monocots.
机译:混合连锁(1,3; 1,4)-beta-glucan(MLG),在零霉病,藻类和无籽血管植物中检测到淘汰的丰富细胞壁多糖,但在无籽血管植物中被检测到,但不在拒于。尽管尚未在苔藓中报道MLG,但是来自苔藓Physcomitrella Patens的预测糖基转移酶(PP3C12_24670)类似于Bona FIDESycete MLG合酶。我们测试了PP3C12_24670通过在野生烟草(Nicotiana Benthamiana)中是否在野外烟草(Nicotiana Benthamiana)中进行编码,并通过结缕碱或(1,4)-β-葡聚糖内加水解酶来测试从细胞壁的诊断寡糖进行测试。 Lichenase,一种MLG特异性内加水解酶,对于来自转化的N型N必需的N必需蛋白,但(1,4)-Beta-glucan内加水解酶释放的寡糖释放的寡糖,该酶与该酶不同于来自MLG的寡糖。进一步的分析表明,这些寡糖衍生自新颖的未经支链未取代的阿拉伯葡聚糖(AGLC)多糖。我们鉴定了与藻类,苔藓植物,溶血性和单偶联物相似的P.Glc合成酶的序列。提高其他早期发散植物合成AGLC的可能性。 P.P.P.P.P.P.pactC的相似性来自ascometes的ascoycetes的MLG合成酶,但不是来自Poaceae的合成酶,表明AGLC和MLG具有常见的进化历史,包括种子植物中的损失,然后是单像中最近的MLG的独立起源。

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  • 来源
    《The Plant Cell》 |2018年第6期|共16页
  • 作者单位

    Univ Rhode Isl Dept Biol Sci Kingston RI 02881 USA;

    Univ Adelaide Sch Agr Food &

    Wine ARC Ctr Excellence Plant Cell Walls Urrbrae SA 5064 Australia;

    Univ Adelaide Sch Agr Food &

    Wine ARC Ctr Excellence Plant Cell Walls Urrbrae SA 5064 Australia;

    Univ Adelaide Sch Agr Food &

    Wine ARC Ctr Excellence Plant Cell Walls Urrbrae SA 5064 Australia;

    Univ Adelaide Sch Agr Food &

    Wine ARC Ctr Excellence Plant Cell Walls Urrbrae SA 5064 Australia;

    Univ Rhode Isl Dept Biol Sci Kingston RI 02881 USA;

    Univ Rhode Isl Dept Biol Sci Kingston RI 02881 USA;

    Univ Adelaide Sch Agr Food &

    Wine ARC Ctr Excellence Plant Cell Walls Urrbrae SA 5064 Australia;

    Univ Melbourne Sch BioSci Plant Cell Biol Res Ctr ARC Ctr Excellence Plant Cell Walls Melbourne Vic 3010 Australia;

    Rhode Isl Coll Dept Biol Providence RI 02908 USA;

    Univ Adelaide Sch Agr Food &

    Wine ARC Ctr Excellence Plant Cell Walls Urrbrae SA 5064 Australia;

    Univ Adelaide Sch Agr Food &

    Wine ARC Ctr Excellence Plant Cell Walls Urrbrae SA 5064 Australia;

    Univ Melbourne Sch BioSci Plant Cell Biol Res Ctr ARC Ctr Excellence Plant Cell Walls Melbourne Vic 3010 Australia;

    Univ Melbourne Sch BioSci Plant Cell Biol Res Ctr ARC Ctr Excellence Plant Cell Walls Melbourne Vic 3010 Australia;

    Univ Adelaide Sch Agr Food &

    Wine ARC Ctr Excellence Plant Cell Walls Urrbrae SA 5064 Australia;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 植物细胞学;
  • 关键词

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