Change in the plasmid copy number in acetic acid Bacteria in response to growth phase and acetic acid Concentration

被引:9
作者
Akasaka, Naoki [1 ]
Astuti, Wiwik [2 ]
Ishii, Yuri [2 ]
Hidese, Ryota [3 ]
Sakoda, Hisao [1 ]
Fujiwara, Shinsuke [2 ,3 ]
机构
[1] Marukan Vinegar Co Ltd, Inst Appl Microbiol, Higashinada Ku, Kobe, Hyogo 6580033, Japan
[2] Kwansei Gakuin Univ, Grad Sch Sci & Technol, Dept Biosci, Sanda, Hyogo 6691337, Japan
[3] Kwansei Gakuin Univ, Grad Sch Sci & Technol, Res Ctr Environm Biosci, Sanda, Hyogo 6691337, Japan
基金
日本学术振兴会;
关键词
Acetic acid bacteria; Gluconacetobacter europaeus; Acetobacter pasteurianus; Plasmid copy number; Real-time quantitative PCR; COMPLETE GENOME SEQUENCE; ACETOBACTER-ACETI; GLUCONACETOBACTER-EUROPAEUS; ESCHERICHIA-COLI; VINEGAR PRODUCTION; DNA-REPLICATION; RESISTANCE; CONSTRUCTION; SYSTEM; TRANSFORMATION;
D O I
10.1016/j.jbiosc.2014.11.003
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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. (C) 2014, The Society for Biotechnology, Japan. All rights reserved.
引用
收藏
页码:661 / 668
页数:8
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