- Mar 2023
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static-content.springer.com static-content.springer.com
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(a)colE1(b)SC101(c)RSF1010
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- Dec 2021
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www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
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. This is the first reported case of conjugative transfer of a naturally occurring plasmid between gram-negative and gram-positive bacteria.
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- Apr 2021
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bmcmicrobiol.biomedcentral.com bmcmicrobiol.biomedcentral.com
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The pUB origin of replication stems from Staphylococcus aureus and is known to be active in a wide range of low GC Gram-positive bacteria (Firmicutes)
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- Dec 2020
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www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
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All replication in R6K relies on the two essential components of a minimal replicon, the γ ori, and its cognate Rep, π protein, encoded by the pir gene
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- Nov 2020
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journals.plos.org journals.plos.org
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Replication begins
Rolling circle replication overview
Replication begins when the Rep protein, which is encoded on the plasmid (ORF A), recognizes a specific site on the plasmid (double-strand origin, or DSO) and catalyzes the nicking of one DNA strand. The Rep protein remains bound to the 5′ phosphate after the nicking action. The newly released 3′ hydroxyl on the opposite end serves as a primer for DNA synthesis. The host DNA polymerase uses the unnicked circular strand as a template, so that a single replication fork moves around a plasmid until it regenerates the DSO. A second copy of Rep protein catalyzes the cleavage of the newly formed DSO, effectively releasing a single stranded copy of the plasmid. In the absence of Rep, the replication fork continues to move around the template, forming a single stranded concatemer. The single strand origin (SSO), a non-coding element that forms extensive secondary structure, is required for synthesis of the lagging strand. SSO sequences vary considerably among different RCR plasmids, but are extremely important for robust replication of the plasmid in the cell [10]. Here we describe the engineering of the pWV01 RCR origin to create pBAV1K-T5, a very broad-host range expression vector.
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