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首页> 外文期刊>Journal of Molecular Structure >Structural and functional insights of beta-glucosidases identified from the genome of Aspergillus fumigatus
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Structural and functional insights of beta-glucosidases identified from the genome of Aspergillus fumigatus

机译:从曲霉菌基因组中鉴定的β-葡糖苷酶的结构和功能见解

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摘要

Thermostable glucose tolerant beta-glucosidase from Aspergillus species has attracted worldwide interest for their potentiality in industrial applications and bioethanol production. A strain of Aspergillus fumigatus (AfNITDGPICA3) identified by our laboratory from straw retting ground showed higher cellulase activity, specifically the beta-glucosidase activity, compared to other contemporary strains. Though A. fumigatus has been known for high cellulase activity, detailed identification and characterization of the cellulase genes from their genome is yet to be done. In this work we have been analyzed the cellulase genes from the genome sequence database of Aspergillus fumigatus (Af293). Genome analysis suggests two cellobiohydrolase, eleven endoglucanase and seventeen beta-glucosidase genes present. beta-Glucosidase genes belong to either Glycohydro1 (GH1 or Bgl1) or Glycohydro3 (GH3 or Bgl3) family. The sequence similarity suggests that Bgl1 and Bgl3 of A. fumagatus are phylogenetically close to those of A. fisheri and A. oryzae. The modelled structure of the Bgl1 predicts the (beta/alpha)(8) barrel type structure with deep and narrow active site, whereas, Bgl3 shows the (alpha/beta)(8) barrel and (alpha/beta)(6) sandwich structure with shallow and open active site. Docking results suggest that amino acids Glu544, Glu466, Trp408,Trp567,Tyr44,-Tyr222,Tyr770,Asp844,Asp537,Asn212,Asn217 of Bgl3 and Asp224,Asn242,Glu440, Glu445, Tyr367, Tyr365,Thr994,Trp435,Trp446 of Bgl1 are involved in the hydrolysis. Binding affinity analyses suggest that Bgl3 and Bgl1 enzymes are more active on the substrates like 4-methylumbelliferyl glycoside (MUG) and p-nitrophenyl-beta-D-1, 4-glucopyranoside (pNPG) than on cellobiose. Further docking with glucose suggests that Bgl1 is more glucose tolerant than Bgl3. Analysis of the Aspergillus fumigatus genome may help to identify a beta-glucosidase enzyme with better property and the structural information may help to develop an engineered re
机译:耐高温糖耐量从曲霉属的β-葡萄糖苷酶已经引起全世界的兴趣为他们在工业应用和生物乙醇的生产潜力。由我们从稻草沤地面实验室鉴定烟曲霉(AfNITDGPICA3)的菌株表现出较高的纤维素酶活性,特别是β-葡糖苷酶活性,相对于其他当代菌株。虽然烟曲霉已经知道高纤维素酶活性,详细的鉴定及鉴定其基因组中纤维素酶基因的尚未完成。在这项工作中,我们已经分析了来自烟曲霉(AF293)的基因组序列数据库中的纤维素酶基因。基因组分析预示了两种纤维二糖水解,十一内切葡聚糖酶十七β-葡萄糖苷酶基因的存在。 β-葡糖苷酶基因属于任一Glycohydro1(GH1或BGL1)或Glycohydro3(GH3或Bgl3)家族。序列相似性表明,BGL1和A. fumagatus的Bgl3在系统发育上接近于A. fisheri和米曲霉的。所述BGL1的建模结构预测(β/α)(8)桶型结构与深而窄的活性位点,反之,Bgl3显示了(α/β)(8)桶和(α/β)(6)夹层结构浅,开放活跃的网站。对接结果表明,氨基酸Glu544,Glu466,Trp408,Trp567,TYR44,-Tyr222,Tyr770,Asp844,Asp537,Asn212,Bgl3和Asp224,Asn242,Glu440,Glu445,Tyr367,Tyr365,Thr994,Trp435,BGL1的Trp446的Asn217参与水解。结合亲和力的分析表明,Bgl3和BGL1酶更活跃像4-甲基伞形酮糖苷(MUG)和对 - 硝基苯基-β-d-1,4-D-吡喃葡萄糖苷(PNPG)比纤维二糖的底物。与葡萄糖进一步对接表明,BGL1更糖耐量比Bgl3。烟曲霉基因组的分析可能有助于确定更好的性能和结构信息的β-葡萄糖苷酶可帮助制定一个重新设计

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