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重組細胞
expressed in corn
形狀
liquid
比活性
0.13 U/mg
環保替代產品特色
Design for Energy Efficiency
Learn more about the Principles of Green Chemistry.
sustainability
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環保替代類別
運輸包裝
dry ice
儲存溫度
−20°C
一般說明
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纤维素水解酶 I 是存在于许多真菌（尤其木腐真菌）中的一种酶。它是 53 kDa 的单体，具有催化结构域和纤维素结合结构域。这个反应将水加到纤维素（糖链的非还原端）的葡萄糖键上，生成纤维二糖。
應用
纤维二糖水解酶I可与内切纤维素酶和b-葡萄糖苷酶结合用于从纤维素中产生葡萄糖。
生化／生理作用
纤维二糖水解酶（CBH）是一种纤维素酶，可通过水解1,4-β-D-糖苷键来降解纤维素。CBH是一种外切纤维素酶，可从纤维素末端切割2至4个单元。CBH I可从还原端逐步切割。CBH I常用于清洁纺织品的洗涤剂中。它在37° C至50° C间存在酶活，最适温度约为45° C。该酶的最适pH为5-6。
單位定義
单位定义：在 50° C、pH 为 5 的条件下，1 个单位每分钟将转化 1 nmole 甲基伞形基 β-D 纤维生物糖苷。
外觀
以硫酸铵沉淀的形式提供，来源为重组玉米。
訊號詞
Danger
危險聲明
危險分類
Resp. Sens. 1
儲存類別代碼
10 - Combustible liquids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
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Zachary K Haviland et al.
The Journal of biological chemistry, 297(3), 101029-101029 (2021-08-03)
Understanding the mechanism by which cellulases from bacteria, fungi, and protozoans catalyze the digestion of lignocellulose is important for developing cost-effective strategies for bioethanol production. Cel7A from the fungus Trichoderma reesei is a model exoglucanase that degrades cellulose strands from
Nicolaj Cruys-Bagger et al.
Biotechnology and bioengineering, 109(12), 3199-3204 (2012-07-07)
An amperometric enzyme biosensor for continuous detection of cellobiose has been implemented as an enzyme assay for cellulases. We show that the initial kinetics for cellobiohydrolase I, Cel7A from Trichoderma reesei, acting on different types of cellulose substrates, semi-crystalline and
Oren Yaniv et al.
Acta crystallographica. Section D, Biological crystallography, 68(Pt 7), 819-828 (2012-07-04)
The crystal structure of the family 3b carbohydrate-binding module (CBM3b) of the cellulosomal multimodular hydrolytic enzyme cellobiohydrolase 9A (Cbh9A) from Clostridium thermocellum has been determined. Cbh9A CBM3b crystallized in space group P4(1) with four molecules in the asymmetric unit and
Kiyohiko Igarashi et al.
Methods in enzymology, 510, 169-182 (2012-05-23)
Cellulases hydrolyze β-1,4-glucosidic linkages of insoluble cellulose at the solid/liquid interface, generating soluble cellooligosaccharides. We describe here our method for real-time observation of the behavior of cellulase molecules on the substrate, using high-speed atomic force microscopy (HS-AFM). When glycoside hydrolase
Larissa C Textor et al.
The FEBS journal, 280(1), 56-69 (2012-11-02)
Aiming to contribute toward the characterization of new, biotechnologically relevant cellulolytic enzymes, we report here the first crystal structure of the catalytic core domain of Cel7A (cellobiohydrolase I) from the filamentous fungus Trichoderma harzianum IOC 3844. Our structural studies and
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Uncover more about glycosaminoglycans and proteoglycans including the structure of glycosaminoglycans (GAGs), the different types of GAGs, and their functions.
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