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醋酸菌中质粒拷贝数随生长阶段和醋酸浓度的变化。

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

作者信息

Akasaka Naoki, Astuti Wiwik, Ishii Yuri, Hidese Ryota, Sakoda Hisao, Fujiwara Shinsuke

机构信息

Institute of Applied Microbiology, Marukan Vinegar Co. Ltd., 5-6 Koyo-cho West, Higashinada-ku, Kobe, Hyogo 658-0033, Japan.

Department of Bioscience, Graduate School of Science and Technology, Kwansei Gakuin University, 2-1 Gakuen, Sanda, Hyogo 669-1337, Japan.

出版信息

J Biosci Bioeng. 2015 Jun;119(6):661-8. doi: 10.1016/j.jbiosc.2014.11.003. Epub 2015 Jan 6.

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.

摘要

从欧洲葡糖醋杆菌KGMA0119中分离出质粒pGE1(2.5 kb)、pGE2(7.2 kb)和pGE3(5.5 kb),序列分析表明它们分别含有3个、8个和4个基因。通过实时定量PCR测定细菌生长不同阶段的质粒拷贝数(PCN)。当KGMA0119在含有0.4%乙醇和0.5%乙酸的培养基中培养时,pGE1的PCN从对数期的7拷贝/基因组增加到稳定期开始时的最高12拷贝/基因组,然后在稳定期末期降至4拷贝/基因组。在整个生长阶段,pGE2和pGE3的PCN维持在1 - 3拷贝/基因组。在较高浓度乙醇(3.2%)下,pGE1在所有生长阶段的PCN略低,而pGE2和pGE3的PCN不变。在存在1.0%乙酸的情况下,对数期pGE1(10拷贝/基因组)和pGE3(6拷贝/基因组)的PCN较高。pGE2的拷贝数没有变化,表明pGE1和pGE3会响应乙酸增加其PCN。通过将线性化的pGE2和pGE3连接到pBR322中构建了质粒pBE2和pBE3。这两种质粒均可在大肠杆菌、巴斯德醋酸杆菌和欧洲葡糖醋杆菌中复制,突出了它们作为醋酸菌载体的适用性。

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