A unique disulfide bridge of the thermophilic xylanase syxyn11 plays a key role in its thermostability

被引:16
作者
Yin, X. [1 ,2 ]
Yao, Y. [3 ]
Wu, M. C. [4 ]
Zhu, T. D. [1 ,2 ]
Zeng, Y. [3 ]
Pang, Q. F. [4 ]
机构
[1] Jiangnan Univ, Minist Educ, Sch Biotechnol, Wuxi 214122, Peoples R China
[2] Jiangnan Univ, Minist Educ, Key Lab Carbohydrate Chem & Biotechnol, Wuxi 214122, Peoples R China
[3] Jiangnan Univ, Sch Pharmaceut Sci, Wuxi 214122, Peoples R China
[4] Jiangnan Univ, Wuxi Med Sch, Wuxi 214122, Peoples R China
关键词
xylanase; thermostability; disulfide bridge; computational prediction; site-directed mutagenesis; TRICHODERMA-REESEI ENDO-1,4-BETA-XYLANASE-II; SECONDARY STRUCTURE; MOLECULAR-DYNAMICS; PICHIA-PASTORIS; GH11; XYLANASE; EXPRESSION; STABILITY; CLONING;
D O I
10.1134/S0006297914060066
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Based on the hyperthermostable family 11 xylanase (EvXyn11(TS)) gene sequence (EU591743), the gene Syxyn11 encoding a thermophilic xylanase SyXyn11 was synthesized with synonymous codons biasing towards Pichia pastoris. The homology alignment of primary structures among family 11 xylanases revealed that, at their N-termini, only SyXyn11 contains a disulfide bridge (Cys5-Cys32). This to some extent implied the significance of the disulfide bridge of SyXyn11 to its thermostability. To confirm the correlation between the N-terminal disulfide bridge and thermostability, a SyXyn11(C5T)-encoding gene, Syxyn11 (C5T), was constructed by mutating the Cys5 codon of Syxyn11 to Thr5. Then, the genes for the recombinant xylanases, reSyXyn11 and reSyXyn11(C5T), were expressed in P. pastoris GS115, yielding xylanase activity of about 35 U per ml cell culture. Both xylanases were purified to homogeneity with specific activities of 363 and 344 U/mg, respectively. The temperature optimum and stability of reSyXyn11(C5T) decreased to 70 and 50A degrees C from 85 and 80A degrees C of reSyXyn11, respectively. There was no obvious change in pH characteristics.
引用
收藏
页码:531 / 537
页数:7
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