Department of Microbiology and Biotechnology, University of Hamburg, Hamburg, Germany.
Methods Mol Biol. 2023;2555:167-179. doi: 10.1007/978-1-0716-2795-2_12.
Metagenomic screening is a widely applied biotechnological approach for screening of novel industrial enzymes. The traditional method of metagenomic screening is based on the functional analyses of heterologously expressed environmental genes in a suitable host, which is the bottleneck of this method. To avoid limitation from the clone-dependent system, an in vitro expression technology has been developed in combination with next-generation sequencing and bioinformatics. First, the sequence profile of a target enzyme, e.g., poly(ethylene terephthalate) esterase in this protocol, is constructed according to the sequences of well-characterized enzymes. Then, the sequence screening is performed with this computationally generated profile among all available metagenomic databases. Afterwards, the candidate genes are synthesized and expressed in vitro with RNA polymerase and translation machinery from special cell extract. Finally, such in vitro produced enzymes are directly applied for the functional analyses. Comparing to the traditional screening methods, this in vitro screening technology can not only save time and materials, but also be easily developed for high-throughput screening with an automatic pipetting robot.
宏基因组筛选是一种广泛应用的生物技术方法,用于筛选新型工业酶。传统的宏基因组筛选方法基于在合适的宿主中异源表达环境基因的功能分析,这是该方法的瓶颈。为了避免克隆依赖性系统的限制,已经开发了一种体外表达技术,结合下一代测序和生物信息学。首先,根据特征明确的酶的序列,构建目标酶(例如本方案中的聚对苯二甲酸乙二醇酯酯酶)的序列特征。然后,使用此计算生成的图谱在所有可用的宏基因组数据库中进行序列筛选。之后,使用特殊细胞提取物中的 RNA 聚合酶和翻译机制合成并体外表达候选基因。最后,直接将体外产生的酶用于功能分析。与传统的筛选方法相比,这种体外筛选技术不仅可以节省时间和材料,而且还可以很容易地开发用于高通量筛选的自动化移液机器人。