Literature DB >> 25575969

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

Naoki Akasaka1, Wiwik Astuti2, Yuri Ishii2, Ryota Hidese3, Hisao Sakoda1, Shinsuke Fujiwara4.   

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.
Copyright © 2014 The Society for Biotechnology, Japan. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Acetic acid bacteria; Acetobacter pasteurianus; Gluconacetobacter europaeus; Plasmid copy number; Real-time quantitative PCR

Mesh:

Substances:

Year:  2015        PMID: 25575969     DOI: 10.1016/j.jbiosc.2014.11.003

Source DB:  PubMed          Journal:  J Biosci Bioeng        ISSN: 1347-4421            Impact factor:   2.894


  7 in total

Review 1.  Beyond horizontal gene transfer: the role of plasmids in bacterial evolution.

Authors:  Jerónimo Rodríguez-Beltrán; Javier DelaFuente; Ricardo León-Sampedro; R Craig MacLean; Álvaro San Millán
Journal:  Nat Rev Microbiol       Date:  2021-01-19       Impact factor: 60.633

Review 2.  On the way toward regulatable expression systems in acetic acid bacteria: target gene expression and use cases.

Authors:  Philipp Moritz Fricke; Angelika Klemm; Michael Bott; Tino Polen
Journal:  Appl Microbiol Biotechnol       Date:  2021-04-15       Impact factor: 4.813

3.  Effective trapping of fruit flies with cultures of metabolically modified acetic acid bacteria.

Authors:  Yuri Ishii; Naoki Akasaka; Itsuko Goda; Hisao Sakoda; Shinsuke Fujiwara
Journal:  Appl Environ Microbiol       Date:  2015-01-16       Impact factor: 4.792

4.  Quantification of Plasmid Copy Number with Single Colour Droplet Digital PCR.

Authors:  Magdalena Plotka; Mateusz Wozniak; Tadeusz Kaczorowski
Journal:  PLoS One       Date:  2017-01-13       Impact factor: 3.240

5.  A genetic toolkit for co-expression of multiple proteins of diverse physiological implication.

Authors:  Ali Samy Abdelaal; Syed Shams Yazdani
Journal:  Biotechnol Rep (Amst)       Date:  2021-12-03

6.  Leucine-Responsive Regulatory Protein in Acetic Acid Bacteria Is Stable and Functions at a Wide Range of Intracellular pH Levels.

Authors:  Yuri Ishii; Yuki Shige; Naoki Akasaka; Afi Candra Trinugraha; Haruka Higashikubo; Wakao Fukuda; Shinsuke Fujiwara
Journal:  J Bacteriol       Date:  2021-08-20       Impact factor: 3.490

7.  Comparative genomics of the Komagataeibacter strains-Efficient bionanocellulose producers.

Authors:  Małgorzata Ryngajłło; Katarzyna Kubiak; Marzena Jędrzejczak-Krzepkowska; Paulina Jacek; Stanisław Bielecki
Journal:  Microbiologyopen       Date:  2018-10-26       Impact factor: 3.139

  7 in total

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