Analysis of a DNA region from low-copy-number plasmid pYAN-1 ofSphingobium yanoikuyaeresponsible for plasmid stability
Author(s) -
Hiroe Hayashi,
Yasuroh Kurusu
Publication year - 2014
Publication title -
bioscience biotechnology and biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.509
H-Index - 116
eISSN - 1347-6947
pISSN - 0916-8451
DOI - 10.1080/09168451.2014.890029
Subject(s) - plasmid , biology , plasmid preparation , genetics , escherichia coli , dna , t dna binary system , low copy number , microbiology and biotechnology , gene , recombinant dna , pbr322 , vector (molecular biology)
We identified and analyzed a DNA region that is required for the stable maintenance of plasmids in the genus Sphingomonas. This DNA fragment, a 244 bp, is localized in the upstream region of the repA gene of low-copy-number small plasmid pYAN-1 (4896 bp) of Sphingobium yanoikuyae. It has four inverted repeats and one direct repeat for possible secondary structures. We were able to stabilize not only another unstable plasmid, pYAN-2, in the genus Sphingomonas, but also the unstable plasmid pSC101 without par locus in Escherichia coli. The copy-number levels between the unstable plasmid and the parental plasmid were similar, and these results suggest that the stabilization of unstable plasmids by this DNA region of pYAN-1 was not due to an increase in plasmid copy number. We concluded that the stabilization of the plasmid was due to a plasmid partition mechanism encoded by a DNA fragment of pYAN-1.
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