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

被引:47
作者
Kotik, Michael [1 ]
机构
[1] Acad Sci Czech Republ, Inst Microbiol, Lab Enzyme Technol, Vvi, CR-14220 Prague 4, Czech Republic
关键词
Metagenome; Consensus sequence; Genome walking; DNA cassette; PCR; MULTIPLE DISPLACEMENT AMPLIFICATION; UNKNOWN FLANKING DNA; RESTRICTION-SITE PCR; DEEP-SEA SEDIMENT; CASSETTE-LIGATION; SOIL METAGENOME; RAPID METHOD; UNCULTURED MICROORGANISMS; OLIGONUCLEOTIDE PRIMERS; HUMIC SUBSTANCES;
D O I
10.1016/j.jbiotec.2009.08.013
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
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. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:75 / 82
页数:8
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