Zeng Wei, Lampugnani Edwin R, Picard Kelsey L, Song Lili, Wu Ai-Min, Farion Isabela M, Zhao Jia, Ford Kris, Doblin Monika S, Bacic Antony
Australian Research Council Centre of Excellence in Plant Cell Walls, School of BioSciences, University of Melbourne, Parkville, Victoria 3010, Australia (W.Z., E.R.L., K.L.P., I.M.F., J.Z., K.F., M.S.D., A.B.);Nurturing Station for the State Key Laboratory of Subtropical Silviculture, Zhejiang A&F University, Lin'an, Hangzhou 311300, China (L.S.); andState Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, South China Agricultural University, Guangzhou 510642, China (A.-M.W.).
Australian Research Council Centre of Excellence in Plant Cell Walls, School of BioSciences, University of Melbourne, Parkville, Victoria 3010, Australia (W.Z., E.R.L., K.L.P., I.M.F., J.Z., K.F., M.S.D., A.B.);Nurturing Station for the State Key Laboratory of Subtropical Silviculture, Zhejiang A&F University, Lin'an, Hangzhou 311300, China (L.S.); andState Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, South China Agricultural University, Guangzhou 510642, China (A.-M.W.)
Plant Physiol. 2016 May;171(1):93-109. doi: 10.1104/pp.15.01919. Epub 2016 Mar 7.
Heteroxylans are abundant components of plant cell walls and provide important raw materials for the food, pharmaceutical, and biofuel industries. A number of studies in Arabidopsis (Arabidopsis thaliana) have suggested that the IRREGULAR XYLEM9 (IRX9), IRX10, and IRX14 proteins, as well as their homologs, are involved in xylan synthesis via a Golgi-localized complex termed the xylan synthase complex (XSC). However, both the biochemical and cell biological research lags the genetic and molecular evidence. In this study, we characterized garden asparagus (Asparagus officinalis) stem xylan biosynthesis genes (AoIRX9, AoIRX9L, AoIRX10, AoIRX14A, and AoIRX14B) by heterologous expression in Nicotiana benthamiana We reconstituted and partially purified an active XSC and showed that three proteins, AoIRX9, AoIRX10, and AoIRX14A, are necessary for xylan xylosyltranferase activity in planta. To better understand the XSC structure and its composition, we carried out coimmunoprecipitation and bimolecular fluorescence complementation analysis to show the molecular interactions between these three IRX proteins. Using a site-directed mutagenesis approach, we showed that the DxD motifs of AoIRX10 and AoIRX14A are crucial for the catalytic activity. These data provide, to our knowledge, the first lines of biochemical and cell biological evidence that AoIRX9, AoIRX10, and AoIRX14A are core components of a Golgi-localized XSC, each with distinct roles for effective heteroxylan biosynthesis.
杂木聚糖是植物细胞壁的丰富成分,为食品、制药和生物燃料行业提供重要原材料。拟南芥(Arabidopsis thaliana)的多项研究表明,不规则木质部9(IRREGULAR XYLEM9,IRX9)、IRX10和IRX14蛋白及其同源物通过一种称为木聚糖合酶复合体(xylan synthase complex,XSC)的高尔基体定位复合体参与木聚糖合成。然而,生化和细胞生物学研究都滞后于遗传和分子证据。在本研究中,我们通过在本氏烟草(Nicotiana benthamiana)中进行异源表达,对芦笋(Asparagus officinalis)茎木聚糖生物合成基因(AoIRX9、AoIRX9L、AoIRX10、AoIRX14A和AoIRX14B)进行了表征。我们重组并部分纯化了一种活性XSC,并表明AoIRX9、AoIRX10和AoIRX14A这三种蛋白是植物中木聚糖木糖基转移酶活性所必需的。为了更好地理解XSC的结构及其组成,我们进行了免疫共沉淀和双分子荧光互补分析,以展示这三种IRX蛋白之间的分子相互作用。使用定点诱变方法,我们表明AoIRX10和AoIRX14A的DxD基序对催化活性至关重要。据我们所知,这些数据提供了首批生化和细胞生物学证据,表明AoIRX9、AoIRX1旦和AoIRX14A是高尔基体定位的XSC的核心成分,每种成分在有效的杂木聚糖生物合成中都具有独特作用。