The effect of some factors on expression of gene encoding endoglucanase from dna metagenome of Binh Chau hot spring in Escherichia coli

T. T. Thuy, L. Nhung, T. Man, L. Xuan, Nguyen Thi Kim Thoa
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Abstract

Expression of microbial target genes in Escherichia coli is broadly used due to its advantages namely: well established system, easy to manipulate, a huge biomass, high level productivity, safe and inexpensive to grow. Metagenomic technique has been applying in Vietnam recently for effective mining of uncultured gene resources, especially in endemic mini-ecologies such as hot springs where the cell densities are low. DNA metagenome of Binh Chau hot spring was isolated and sequenced by Illumia HiseqTM. Based on analyses of databases of cellulase-encoded genes, denovogenes 18736 gene sequence for thermal endoglucanase was selected for expression in E. coli. In this paper, some factors for expression of endoglucanase have been investigated. The results show that appropriate gene expression conditions are:  Expression performed in E. coli C43 (DE3) on TB medium at 30oC with 0.25 mM of IPTG as inducer, the culture volume of 20% compared with the bottle volume and the expression time is 42–48 hours. In this condition, the biomass production and soluble enzyme activity can reached up to 5.54–5.58 g /L and  1.92–1.98 U/mL, respectively. Our results show the prospect of exploiting microbial genes without culture.
平洲温泉大肠杆菌dna宏基因组中编码内切葡聚糖酶基因表达的影响
在大肠杆菌中表达微生物靶基因具有体系完善、易于操作、生物量大、生产率高、安全、成本低等优点,被广泛应用。近年来,宏基因组技术在越南被广泛应用于非养殖基因资源的有效挖掘,特别是在温泉等细胞密度低的地方性微型生态环境中。利用Illumia HiseqTM对平洲温泉的DNA宏基因组进行了分离和测序。在分析纤维素酶编码基因数据库的基础上,选择热内切葡聚糖酶的denvogenes 18736基因序列在大肠杆菌中表达。本文对影响内切葡聚糖酶表达的一些因素进行了研究。结果表明,适宜的基因表达条件为:大肠杆菌C43 (DE3)在TB培养基上以0.25 mM IPTG为诱导剂,30℃下进行表达,培养量为瓶体积的20%,表达时间为42 ~ 48小时。在此条件下,生物量可达5.54 ~ 5.58 g /L,可溶性酶活性可达1.92 ~ 1.98 U/mL。我们的研究结果显示了利用微生物基因无需培养的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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