Takahashi Masato, Sawada Yoshisuke, Aoyagi Hideki
Division of Life Sciences and Bioengineering, Graduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki, 305-8572, Japan.
Iwashiya Bio Science, Inc., 2-18-4, Higashi Shinmachi, Itabashi-ku, Tokyo, 174-0074, Japan.
AMB Express. 2017 Aug 23;7(1):163. doi: 10.1186/s13568-017-0464-4.
Monitoring the environmental factors during shake-flask culture of microorganisms can help to optimise the initial steps of bioprocess development. Herein, we developed a circulation direct monitoring and sampling system (CDMSS) that can monitor the behaviour of CO and O in the gas-liquid phases and obtain a sample without interrupting the shaking of the culture in Erlenmeyer flasks capped with breathable culture plugs. Shake-flask culturing of Escherichia coli using this set-up indicated that a high concentration of CO accumulated not only in the headspace (maximum ~100 mg/L) but also in the culture broth (maximum ~85 mg/L) during the logarithmic phase (4.5-9.0 h). By packing a CO absorbent in the gas circulation unit of CDMSS, a specialised shake-flask culture was developed to remove CO from the headspace. It was posited that removing CO from the headspace would suppress increases in the dissolved CO concentration in the culture broth (maximum ~15 mg/L). Furthermore, the logarithmic growth phase (4.5-12.0 h) was extended, the U.O.D. and pH value increased, and acetic acid concentration was reduced, compared with the control. To our knowledge, this is the first report of a method aimed at improving the growth of E. coli cells without changing the composition of the medium, temperature, and shaking conditions.
在微生物摇瓶培养过程中监测环境因素有助于优化生物工艺开发的初始步骤。在此,我们开发了一种循环直接监测与采样系统(CDMSS),该系统能够监测气液相中CO和O的行为,并在使用透气培养塞封口的锥形瓶中不中断培养物振荡的情况下获取样品。使用该装置对大肠杆菌进行摇瓶培养表明,在对数生长期(4.5 - 9.0小时),高浓度的CO不仅在顶空积累(最高约100 mg/L),而且在培养液中积累(最高约85 mg/L)。通过在CDMSS的气体循环单元中填充CO吸收剂,开发了一种专门的摇瓶培养方法以从顶空中去除CO。据推测,从顶空中去除CO将抑制培养液中溶解CO浓度的增加(最高约15 mg/L)。此外,与对照相比,对数生长期(4.5 - 12.0小时)延长,溶解氧和pH值增加,乙酸浓度降低。据我们所知,这是第一篇关于在不改变培养基成分、温度和振荡条件的情况下旨在改善大肠杆菌细胞生长的方法的报道。