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A highly efficient targeted recombination system for engineering linear chromosomes of industrial bacteria Streptomyces

期刊

JOURNAL OF GENERAL AND APPLIED MICROBIOLOGY
卷 64, 期 4, 页码 167-173

出版社

MICROBIOL RES FOUNDATION
DOI: 10.2323/jgam.2017.11.004

关键词

genome engineering; linear chromosome; linear plasmid; Streptomyces; targeted recombination

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  1. Ministry of Science and Technology, Republic of China [96-2628-B-027-001-MY3]

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Soil bacteria Streptomyces are the most important producers of secondary metabolites, including most known antibiotics. These bacteria and their close relatives are unique in possessing linear chromosomes, which typically harbor 20 to 30 biosynthetic gene clusters of tens to hundreds of kb in length. Many Streptomyces chromosomes are accompanied by linear plasmids with sizes ranging from several to several hundred kb. The large linear plasmids also often contain biosynthetic gene clusters. We have developed a targeted recombination procedure for arm exchanges between a linear plasmid and a linear chromosome. A chromosomal segment inserted in an artificially constructed plasmid allows homologous recombination between the two replicons at the homology. Depending on the design, the recombination may result in two recombinant replicons or a single recombinant chromosome with the loss of the recombinant plasmid that lacks a replication origin. The efficiency of such targeted recombination ranges from 9 to 83% depending on the locations of the homology (and thus the size of the chromosomal arm exchanged), essentially eliminating the necessity of selection. The targeted recombination is useful for the efficient engineering of the Streptomyces genome for large-scale deletion, addition, and shuffling.

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