首页> 美国卫生研究院文献>Applied and Environmental Microbiology >Heterologous expression of endo-beta-14-D-glucanase from Clostridium cellulovorans in Clostridium acetobutylicum ATCC 824 following transformation of the engB gene.
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Heterologous expression of endo-beta-14-D-glucanase from Clostridium cellulovorans in Clostridium acetobutylicum ATCC 824 following transformation of the engB gene.

机译:engB基因转化后在丙酮丁醇梭菌ATCC 824中来自纤维素梭菌的内切β-14-D-葡聚糖酶的异源表达。

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摘要

Heterologous expression of the Clostridium cellulovorans engB gene by Clostridium acetobutylicum BKW-1 was detected as zones of hydrolysis on carboxymethyl cellulose (CMC) Trypticase glucose yeast plates stained with Congo red. The extracellular cellulase preparation from C. acetobutylicum BKW-1 has a specific activity towards CMC which is more than fourfold that present in C. acetobutylicum ATCC 824. Western blot (immunoblot) analysis using the C. cellulovorans anti-EngB primary antibody demonstrated that an additional 44-kDa protein band was present in the supernatant derived from C. acetobutylicum BKW-1 but was not present in ATCC 824 or ATCC 824(pMTL500E).
机译:检测丙酮丁醇梭菌BKW-1异纤梭菌engB基因的异源表达,并将其标记为用刚果红​​染色的羧甲基纤维素(CMC)胰蛋白酶葡萄糖酵母平板上的水解区域。丙酮丁醇梭菌BKW-1的细胞外纤维素酶制剂对CMC的特异性活性是丙酮丁醇梭菌ATCC 824的四倍以上。使用纤维素丙种梭菌抗EngB一抗的蛋白质印迹(免疫印迹)分析表明,在来自丙酮丁醇梭菌BKW-1的上清液中存在另外的44kDa蛋白带,但是在ATCC 824或ATCC 824(pMTL500E)中不存在。

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