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Change in the plasmid copy number in acetic acid bacteria in response to growth phase and acetic acid concentration.

Authors :
Akasaka N
Astuti W
Ishii Y
Hidese R
Sakoda H
Fujiwara S
Source :
Journal of bioscience and bioengineering [J Biosci Bioeng] 2015 Jun; Vol. 119 (6), pp. 661-8. Date of Electronic Publication: 2015 Jan 06.
Publication Year :
2015

Abstract

Plasmids pGE1 (2.5 kb), pGE2 (7.2 kb), and pGE3 (5.5 kb) were isolated from Gluconacetobacter europaeus KGMA0119, and sequence analyses revealed they harbored 3, 8, and 4 genes, respectively. Plasmid copy numbers (PCNs) were determined by real-time quantitative PCR at different stages of bacterial growth. When KGMA0119 was cultured in medium containing 0.4% ethanol and 0.5% acetic acid, PCN of pGE1 increased from 7 copies/genome in the logarithmic phase to a maximum of 12 copies/genome at the beginning of the stationary phase, before decreasing to 4 copies/genome in the late stationary phase. PCNs for pGE2 and pGE3 were maintained at 1-3 copies/genome during all phases of growth. Under a higher concentration of ethanol (3.2%) the PCN for pGE1 was slightly lower in all the growth stages, and those of pGE2 and pGE3 were unchanged. In the presence of 1.0% acetic acid, PCNs were higher for pGE1 (10 copies/genome) and pGE3 (6 copies/genome) during the logarithmic phase. Numbers for pGE2 did not change, indicating that pGE1 and pGE3 increase their PCNs in response to acetic acid. Plasmids pBE2 and pBE3 were constructed by ligating linearized pGE2 and pGE3 into pBR322. Both plasmids were replicable in Escherichia coli, Acetobacter pasteurianus and G. europaeus, highlighting their suitability as vectors for acetic acid bacteria.<br /> (Copyright © 2014 The Society for Biotechnology, Japan. Published by Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1347-4421
Volume :
119
Issue :
6
Database :
MEDLINE
Journal :
Journal of bioscience and bioengineering
Publication Type :
Academic Journal
Accession number :
25575969
Full Text :
https://doi.org/10.1016/j.jbiosc.2014.11.003