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Original molecular cloning vectors were plasmids such as the pBR232, were meant to clone single genes, and were based in multicopy plasmids that have low stringency control of the copy number. Later on with the development of genomics, larger insert vectors were required for the assembly of repeated regions and in general to pair-end the individual shotgun reads. Bacterial artificial chromosomes (BAC) were developed based in the large single-copy plasmids of the F group (Shizuya et al. 1992). These can be propagated in Escherichia coli with inserts larger than 300 Kbp. BACs were used by Beja and coworkers in one of the first and more influential papers of the early development of metagenomics in which the existence of an energy-generating rhodopsin was found in a proteobacterial BAC clone (Beja et al. 2000). However, BACs are laborious to generate and do not work well with the limited amount of DNA that normally is available for...
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Rodriguez-Valera, F. (2013). Fosmid System. In: Nelson, K. (eds) Encyclopedia of Metagenomics. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-6418-1_115-3
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DOI: https://doi.org/10.1007/978-1-4614-6418-1_115-3
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