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Novel genes retrieved from environmental DNA by polymerase chain reaction: Current genome-walking techniques for future metagenome applications

机译:通过聚合酶链反应从环境DNA中检索到的新基因:用于未来的基因组学应用的当前基因组遍历技术

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摘要

Environmental DNA is an extremely rich source of genes encoding enzymes with novel biocatalytic activities. To tap this source, function-based and sequence-based strategies have been established to isolate, clone, and express these novel metagenome-derived genes. Sequence-based strategies, which rely on PCR with consensus primers and genome walking, represent an efficient and inexpensive alternative to activity-based screening of recombinant strains harbouring fragments of environmental DNA. This review covers the diverse array of genome-walking techniques, which were originally developed for genomic DNA and currently are also used for PCR-based recovery of entire genes from the metagenome. These sequence-based gene mining methods appear to offer a powerful tool for retrieving from the metagenome novel genes encoding biocatalysts with potential applications in biotechnology.
机译:环境DNA是编码具有新生物催化活性的酶的基因的极其丰富的来源。为了利用这一资源,已经建立了基于功能和基于序列的策略来分离,克隆和表达这些新颖的基因组学衍生基因。基于序列的策略依赖于具有共有引物的PCR和基因组步移,是一种有效且廉价的替代方法,可替代基于活性的,筛选环境DNA片段的重组菌株。这篇综述涵盖了各种各样的基因组遍历技术,这些技术最初是为基因组DNA开发的,目前也用于基于基因组学的基于PCR的完整基因组回收。这些基于序列的基因挖掘方法似乎提供了一个强大的工具,可以从元基因组中检索编码生物催化剂的新基因,并将其应用于生物技术中。

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