Expression and processing of a major xylanase (XYN2) from the thermophilic fungus Humicola grisea var. thermoidea in Trichoderma reesei

被引:48
作者
de Faria, FP
Te'o, VSJ
Bergquist, PL
Azevedo, MO
Nevalainen, KMH [1 ]
机构
[1] Macquarie Univ, Dept Biol Sci, Sydney, NSW 2109, Australia
[2] FAENQUIL, Dept Biotecnol, Lorena, SP, Brazil
[3] Univ Auckland, Sch Med, Div Mol Med, Auckland, New Zealand
[4] Univ Brasilia, IB, Dept Biol Celular, Brasilia, DF, Brazil
关键词
D O I
10.1046/j.1472-765x.2002.01057.x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aims: To express a gene encoding a heterologous fungal xylanase in Trichoderma reesei. Methods and Results: Humicola grisea xylanase 2 (xyn2) cDNA was expressed in Trichoderma reesei under the main cellobiohydrolase I (cbh1) promoter (i) as a fusion to the cellobiohydrolase I (CBHI) secretion signal and (ii) the mature CBHI core-linker. The recombinant xylanase (HXYN2) was secreted into the cultivation medium and processed in a similar fashion to the endogenous T. reesei xylanases, resulting in an active enzyme. Conclusions, Significance and Impact of the Study: HXYN2 was successfully processed in T. reesei. Composition of the culture medium affected the HXYN2 yields, favouring Avicel-lactose as a carbon source. Best yields (about 0.5 g l(-1)) in shake flask cultivations were obtained from a transformant where xyn2 was fused directly to the CBHI secretion signal.
引用
收藏
页码:119 / 123
页数:5
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