Effect of N-terminal disulfide bridge on thermostability of family 11 xylanases / 生物工程学报
Chinese Journal of Biotechnology
; (12): 1441-1449, 2012.
Article
in Zh
| WPRIM
| ID: wpr-342382
Responsible library:
WPRO
ABSTRACT
A mesophilic xylanase from Aspergillus oryzae, abbreviated to AoXyn11A, belongs to glycoside hydrolase family 11. Using AoXyn11A as the parent, the thermotolerant hybrid xylanase, we constructed AEx11A by substituting its N-terminus with the corresponding region of a hyperthermostable family 11 xylanase, EvXyn11(TS). AoXyn11A- and AEx11A-encoding genes were expressed in Pichia pastoris GS115 separately, and effects of temperatures on expressed products were determined and compared. The optimum temperature (T(opt)) of AEx11A was 75 degrees C and its half-life at 70 degrees C (t1/2(70)) was 197 min, improved as compared with those (T(opt) = 50 degrees C, t1/2(70) = 1.0 min) of AoXyn11A. Homology modeling of the AEx11A's structure and comparison between structures of AEx11A and AoXyn11A revealed that one disulfide bridge (Cys5-Cys32) was introduced into AEx11A resulted from N-terminus substitution. To explore the effect of the disulfide bridge on the thermostability of AEx11A, it was removed from AEx11A by site-directed mutagenesis (C5T). Analytical results show that the T(opt) of the mutant AEx11A (AEx11A(C5T)) dropped to 60 degrees C from 75 degrees C of AEx11A, and its t1/2(70) and t1/2(80) also decreased to 3.0 and 1.0 min from 197 and 25 min.
Full text:
1
Database:
WPRIM
Main subject:
Pichia
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Aspergillus oryzae
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Enzyme Stability
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Recombinant Proteins
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Molecular Sequence Data
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Base Sequence
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Protein Engineering
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Chemistry
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Mutagenesis, Site-Directed
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Amino Acid Sequence
Language:
Zh
Journal:
Chinese Journal of Biotechnology
Year:
2012
Document type:
Article