Purification, crystallization and preliminary crystallographic analysis of the catalytic domain of the extracellular cellulase CBHI from Trichoderma harzianum

被引:6
|
作者
Colussi, Francieli [1 ]
Textor, Larissa C. [1 ]
Serpa, Viviane [1 ]
Maeda, Roberto Nobuyuki [2 ]
Pereira, Nei, Jr. [2 ]
Polikarpov, Igor [1 ]
机构
[1] Univ Sao Paulo, Inst Fis Sao Carlos, BR-13560970 Sao Carlos, SP, Brazil
[2] Univ Fed Rio de Janeiro, Ctr Tecnol, Escola Quim, Lab Desenvolvimento Bioprocessos LaDeBio, BR-21949900 Rio De Janeiro, Brazil
来源
ACTA CRYSTALLOGRAPHICA SECTION F-STRUCTURAL BIOLOGY COMMUNICATIONS | 2010年 / 66卷
基金
巴西圣保罗研究基金会;
关键词
cellobiohydrolases; Trichoderma harzianum; cellulases; CELLOBIOHYDROLASE-I; REESEI CELLOBIOHYDROLASES; ENDOGLUCANASE-II; IDENTIFICATION; ENZYMES;
D O I
10.1107/S1744309110026886
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The filamentous fungus Trichoderma harzianum has a considerable cellulolytic activity that is mediated by a complex of enzymes which are essential for the hydrolysis of microcrystalline cellulose. These enzymes were produced by the induction of T. harzianum with microcrystalline cellulose (Avicel) under submerged fermentation in a bioreactor. The catalytic core domain (CCD) of cellobiohydrolase I (CBHI) was purified from the extracellular extracts and submitted to robotic crystallization. Diffraction-quality CBHI CCD crystals were grown and an X-ray diffraction data set was collected under cryogenic conditions using a synchrotron-radiation source.
引用
收藏
页码:1041 / 1044
页数:4
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