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Xylan Utilization Regulon in Xanthomonas citri pv. citri Strain 306: Gene Expression and Utilization of Oligoxylosides

机译:Xanthomonas citri pv中的木聚糖利用法规。柠檬菌株306:低聚果糖苷的基因表达与利用

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Xanthomonas citri pv. citri strain 306 ( Xcc 306), a causative agent of citrus canker, produces endoxylanases that catalyze the depolymerization of cell wall-associated xylans. In the sequenced genomes of all plant-pathogenic xanthomonads, genes encoding xylanolytic enzymes are clustered in three adjacent operons. In Xcc 306, these consecutive operons contain genes encoding the glycoside hydrolase family 10 (GH10) endoxylanases Xyn10A and Xyn10C, the agu67 gene, encoding a GH67 α-glucuronidase (Agu67), the xyn43E gene, encoding a putative GH43 α-l-arabinofuranosidase, and the xyn43F gene, encoding a putative β-xylosidase. Recombinant Xyn10A and Xyn10C convert polymeric 4- O -methylglucuronoxylan (MeGX_( n )) to oligoxylosides methylglucuronoxylotriose (MeGX_(3)), xylotriose (X_(3)), and xylobiose (X_(2)). Xcc 306 completely utilizes MeGX_( n ) predigested with Xyn10A or Xyn10C but shows little utilization of MeGX_( n ). Xcc 306 with a deletion in the gene encoding α-glucuronidase ( Xcc 306 Δ agu67 ) will not utilize MeGX_(3) for growth, demonstrating the role of Agu67 in the complete utilization of GH10-digested MeGX_( n ). Preferential growth on oligoxylosides compared to growth on polymeric MeGX_( n ) indicates that GH10 xylanases, either secreted by Xcc 306 in planta or produced by the plant host, generate oligoxylosides that are processed by Xyn10 xylanases and Agu67 residing in the periplasm. Coordinate induction by oligoxylosides of xyn10 , agu67 , cirA , the tonB receptor, and other genes within these three operons indicates that they constitute a regulon that is responsive to the oligoxylosides generated by the action of Xcc 306 GH10 xylanases on MeGX_( n ). The combined expression of genes in this regulon may allow scavenging of oligoxylosides derived from cell wall deconstruction, thereby contributing to the tissue colonization and/or survival of Xcc 306 and, ultimately, to plant disease.
机译:Xanthomonas citri pv。柑橘溃疡病的病原体柠檬酸菌株306(Xcc 306)产生内切木聚糖酶,催化与细胞壁相关的木聚糖解聚。在所有植物病原体黄单胞菌的测序基因组中,编码木聚糖分解酶的基因聚集在三个相邻的操纵子中。在Xcc 306中,这些连续的操纵子包含编码糖苷水解酶家族10(GH10)内切木聚糖酶Xyn10A和Xyn10C的基因,agu67基因编码GH67α-葡萄糖醛酸糖苷酶(Agu67),xyn43E基因编码推定的GH43α-1-阿拉伯呋喃糖苷酶,和xyn43F基因,编码一个假定的β-木糖苷酶。重组Xyn10A和Xyn10C将聚合的4- O-甲基葡糖醛酸木聚糖(MeGX_(n))转化为低聚果糖甲基葡糖醛酸木糖(MeGX_(3)),木糖三糖(X_(3))和木糖(X_(2))。 Xcc 306完全利用Xyn10A或Xyn10C预先消化的MeGX_(n),但对MeGX_(n)的利用很少。在编码α-葡萄糖醛酸苷酶(Xcc 306Δagu67)的基因中缺失的Xcc 306将不会利用MeGX_(3)进行生长,这表明Agu67在完全利用GH10消化的MeGX_(n)中的作用。与在聚合MeGX_(n)上的生长相比,低聚环氧乙烷的优先生长表明,GH10木聚糖酶(由植物中的Xcc 306分泌或由植物宿主产生)生成由Xyn10木聚糖酶和存在于周质中的Agu67处理的低聚环氧乙烷。在这三个操纵子中xyn10,agu67,cirA,tonB受体和其他基因的低聚氧苷的坐标诱导表明,它们构成了对Xcc 306 GH10木聚糖酶对MeGX_(n)作用产生的低聚氧苷响应的调节子。基因在该调节子中的联合表达可允许清除源自细胞壁解构的寡聚氧苷,从而有助于组织定植和/或Xcc 306的存活,并最终导致植物病害。

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