Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/95657
標題: Deciphering characteristics of the designer cellulosome from Bacillus subtilis WB800N via enzymatic analysis
作者: Chia-Chi Lin
Cally Joe San Yap
Shu-Chen Kan
Nai-Chi Hsueh
Liang-Yu Yang
Chwen-Jen Shieh
Chieh-Chen Huang
劉永銓
Yung-Chuan Liu
關鍵字: Biodegradation
Cellulase
Enzyme technology
Kinetic parameters
Designer cellulosome
Zymographic assay
出版社: BIOCHEMICAL ENGINEERING JOURNAL
摘要: Recombinant Bacillus subtilis WB800N harboring pGETS 118 designer cellulosome genes was applied to the artificial cellulosome production. To investigate the characteristics of cellulosome assembly in the supernatant, three free enzymes clones, i.e., endoglucanase, exoglucanase and xylanase, were constructed. The samples of the respective free enzymes and the cellulosome were collected and examined via various enzymatic assays. In comparison of specific activity of anchored cellulosome and the free enzymes on cell pellets, it was found that only anchored cellulosome exhibited the activities. No activity was detected on the cell pellets of the three free enzyme clones. This indicated that the designer cellulosome subunits must be properly self-assembled into a substantial complex capable of the cellulose degradation. To study the cellulose hydrolytic behavior, the best specific activities of endoglucanase and xylanase obtained in the supernatant cellulosome were 3.62 ± 0.02 U/mg and 1.97 ± 0.06 U/mg, respectively. The end products of the enzyme reaction detected via HPLC analysis showed that oligosaccharide and cellobiose were the major products in the hydrolytic reactions. In the kinetic studies, the Vmax value (8.98 mM/h) for endoglucanase in the supernatant cellulosome was higher than pellets (0.603 mM/h). However, the endoglucanase of pellets gave a lower Km value of 0.359 g/L, indicating a higher substrate affinity than that in the supernatant (11.87 g/L).
URI: http://hdl.handle.net/11455/95657
文章連結: https://www.sciencedirect.com/science/article/pii/S1369703X16302716
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