首页> 外文期刊>Applied Microbiology >S-Layer Homology Domain Proteins Csac_0678 and Csac_2722 Are Implicated in Plant Polysaccharide Deconstruction by the Extremely Thermophilic Bacterium Caldicellulosiruptor saccharolyticus
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S-Layer Homology Domain Proteins Csac_0678 and Csac_2722 Are Implicated in Plant Polysaccharide Deconstruction by the Extremely Thermophilic Bacterium Caldicellulosiruptor saccharolyticus

机译:S层同源域蛋白Csac_0678和Csac_2722涉及极端嗜热细菌Caldicellulosiruptor saccharolyticus的植物多糖解构。

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The genus Caldicellulosiruptor contains extremely thermophilic bacteria that grow on plant polysaccharides. The genomes of Caldicellulosiruptor species reveal certain surface layer homology (SLH) domain proteins that have distinguishing features, pointing to a role in lignocellulose deconstruction. Two of these proteins in Caldicellulosiruptor saccharolyticus (Csac_0678 and Csac_2722) were examined from this perspective. In addition to three contiguous SLH domains, the Csac_0678 gene encodes a glycoside hydrolase family 5 (GH5) catalytic domain and a family 28 carbohydrate-binding module (CBM); orthologs to Csac_0678 could be identified in all genome-sequenced Caldicellulosiruptor species. Recombinant Csac_0678 was optimally active at 75°C and pH 5.0, exhibiting both endoglucanase and xylanase activities. SLH domain removal did not impact Csac_0678 GH activity, but deletion of the CBM28 domain eliminated binding to crystalline cellulose and rendered the enzyme inactive on this substrate. Csac_2722 is the largest open reading frame (ORF) in the C. saccharolyticus genome (predicted molecular mass of 286,516 kDa) and contains two putative sugar-binding domains, two Big4 domains (bacterial domains with an immunoglobulin [Ig]-like fold), and a cadherin-like (Cd) domain. Recombinant Csac_2722, lacking the SLH and Cd domains, bound to cellulose and had detectable carboxymethylcellulose (CMC) hydrolytic activity. Antibodies directed against Csac_0678 and Csac_2722 confirmed that these proteins bound to the C. saccharolyticus S-layer. Their cellular localization and functional biochemical properties indicate roles for Csac_0678 and Csac_2722 in recruitment and hydrolysis of complex polysaccharides and the deconstruction of lignocellulosic biomass. Furthermore, these results suggest that related SLH domain proteins in other Caldicellulosiruptor genomes may also be important contributors to plant biomass utilization.
机译:Caldicellulosiruptor属包含在植物多糖上生长的极嗜热细菌。 Caldicellulosiruptor物种的基因组揭示了某些具有独特特征的表面层同源性(SLH)域蛋白,指出了木质纤维素解构中的作用。从这个角度检查了解糖卡尔德氏菌中的两个蛋白质(Csac_0678和Csac_2722)。除了三个连续的SLH域外,Csac_0678基因还编码一个糖苷水解酶5族(GH5)催化域和一个28族碳水化合物结合模块(CBM)。 Csac_0678的直系同源物可以在所有基因组测序的Caldicellulosiruptor物种中找到。重组Csac_0678在75°C和pH 5.0时具有最佳活性,同时具有内切葡聚糖酶和木聚糖酶活性。 SLH结构域的去除不会影响Csac_0678 GH的活性,但是CBM28结构域的缺失消除了与结晶纤维素的结合,并使酶对该底物失去活性。 Csac_2722是解糖梭菌基因组中最大的开放阅读框(ORF)(预测分子量为286,516 kDa),包含两个推定的糖结合域,两个Big4域(具有免疫球蛋白[Ig]样折叠的细菌域),和钙粘蛋白样(Cd)域。缺少SLH和Cd域的重组Csac_2722与纤维素结合,并具有可检测的羧甲基纤维素(CMC)水解活性。针对Csac_0678和Csac_2722的抗体证实,这些蛋白与解糖梭菌S层结合。它们的细胞定位和功能生化特性表明Csac_0678和Csac_2722在复杂多糖的募集和水解以及木质纤维素生物质解构中的作用。此外,这些结果表明,其他Caldicellulosiruptor基因组中的相关SLH域蛋白也可能是植物生物量利用的重要贡献者。

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