Expression of multi-functional cellulase gene mfc in Coprinus cinereus under control of different basidiomycete promoters

被引:30
作者
Cheng, Shujie [1 ,2 ]
Yang, Peizhou [1 ,3 ]
Guo, Liqiong [1 ,2 ]
Lin, Junfang [1 ,2 ]
Lou, Nannan [1 ,2 ]
机构
[1] S China Agr Univ, Coll Food Sci, Dept Bioengn, Guangzhou 510640, Peoples R China
[2] S China Agr Univ, Inst Biomass Res, Guangzhou 510640, Peoples R China
[3] Hefei Univ Technol, Sch Biotechnol & Food Engn, Hefei 230009, Peoples R China
基金
中国国家自然科学基金;
关键词
Multi-functional cellulase; Endo-beta-1,4-glucanase; Endo-beta-1,4-xylanase; Coprinus cinereus; Basidiomycete promoters; COPRINOPSIS-CINEREA; MEDIATED TRANSFORMATION; AGARICUS-BISPORUS; XYLANASE GENE; LACCASE; CLONING;
D O I
10.1016/j.biortech.2009.04.021
中图分类号
S2 [农业工程];
学科分类号
0828 ;
摘要
Multi-functional cellulase gene infc was expressed in Coprinus cinereus under naturally non-inductive conditions using three heterologous promoters. Endo-beta-1,4-glucanase expression was achieved in solid and liquid media with promoter sequences from the Lentinula edodes gpd gene, the Flammulina velutipes gpd gene and the Volvariella volvacea gpd gene. As measured by enzyme activity in liquid cultures, a 613-bp gpd promoter fragment from L. edodes was most efficient. followed by a 752-bp gpd fragment from F. velutipes. The V. volvacea gpd promoter sequence was less active, in comparison. Irrespective of the promoter used, enzymatic activities increase 34-fold for highly active transformants and 29-fold for less active one by using cellulase-inducing medium. The highest activities of endo-beta-1,4-glucanase (34.234 U/ml) and endo-beta-1,4-xylanase (263.695 U/ml) were reached by using the L. edodes gpd promoter. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4475 / 4480
页数:6
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