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首页> 外文期刊>Proteins: Structure, Function, and Genetics >Distinctive ligand‐binding specificities of tandem PA14 biomass‐sensory elements from Clostridium thermocellum Clostridium thermocellum and Clostridium clariflavum Clostridium clariflavum
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Distinctive ligand‐binding specificities of tandem PA14 biomass‐sensory elements from Clostridium thermocellum Clostridium thermocellum and Clostridium clariflavum Clostridium clariflavum

机译:串联PA14生物质感觉元素的独特配体结合特异性来自Clostridium Thermocellum Clostridium Thermocellum和Clostriflavum Clostridium Clariflavum

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摘要

Abstract Cellulolytic clostridia use a highly efficient cellulosome system to degrade polysaccharides. To regulate genes encoding enzymes of the multi‐enzyme cellulosome complex, certain clostridia contain alternative sigma I (σ I ) factors that have cognate membrane‐associated anti‐σ I factors (RsgIs) which act as polysaccharide sensors. In this work, we analyzed the structure‐function relationship of the extracellular sensory elements of Clostridium ( Ruminiclostridium) thermocellum and Clostridium clariflavum (RsgI3 and RsgI4, respectively). These elements were selected for comparison, as each comprised two tandem PA14‐superfamily motifs. The X‐ray structures of the PA14 modular dyads from the two bacterial species were determined, both of which showed a high degree of structural and sequence similarity, although their binding preferences differed. Bioinformatic approaches indicated that the DNA sequence of promoter of sigI / rsgI operons represents a strong signature, which helps to differentiate binding specificity of the structurally similar modules. The σ I4 ‐dependent C. clariflavum promoter sequence correlates with binding of RsgI4_PA14 to xylan and was identified in genes encoding xylanases, whereas the σ I3 ‐dependent C. thermocellum promoter sequence correlates with RsgI3_PA14 binding to pectin and regulates pectin degradation‐related genes. Structural similarity between clostridial PA14 dyads to PA14‐containing proteins in yeast helped identify another crucial signature element: the calcium‐binding loop 2 (CBL2), which governs binding specificity. Variations in the five amino acids that constitute this loop distinguish the pectin vs xylan specificities. We propose that the first module (PA14 A ) is dominant in directing the binding to the ligand in both bacteria. The two X‐ray structures of the different PA14 dyads represent the first reported structures of tandem PA14 modules.
机译:摘要纤维素分解梭菌利用高效的纤维素体系来降解多糖。为了调节编码多酶纤维素体复合物的酶的基因,某些蛋白酶含有具有同源膜相关的抗-Σi因子(RSGIS)的替代Sigma I(σi)因子,其充当多糖传感器。在这项工作中,我们分析了梭菌(Ruminiclostridium)热团块和蛋黄酸纤维蛋白酶和蛋酸纤维蛋白酶(RSGI3和RSGI4)的细胞外感觉元件的结构功能关系。选择这些元素进行比较,因为每个元素包括两个串联PA14-超家谱基序。确定来自两种细菌种类的PA14模块化二元的X射线结构,两者都显示出高度的结构和序列相似性,尽管它们的结合偏好不同。生物信息化方法表明,SIGI / RSGI操纵子的启动子DNA序列代表强签名,这有助于区分结构上类似模块的结合特异性。 σ14依赖性C.克拉芬兰螺旋蛋白序列与RSGI4_PA14至木聚糖的结合相关,并在编码木聚糖酶的基因中鉴定出来,而σ13依赖性C.热膨胀者促进剂序列与RSGI3_PA14与果胶结合并调节果胶降解相关基因。酵母中含有含有Pa14的蛋白质之间的梭菌PA14α的结构相似有助于鉴定另一种关键的签名元件:钙结合环2(CBL2),其治理结合特异性。构成该回路的五个氨基酸的变化区分果胶与木聚糖的特异性。我们提出第一模块(PA14a)的主导地在两种细菌中引导与配体中的结合。不同PA14 DYADS的两个X射线结构代表了串联PA14模块的第一个报告的结构。

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