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Development of an Optimized Medium Strain and High-Throughput Culturing Methods for Methylobacterium extorquens

机译:甲基芽胞杆菌优化培养基菌株和高通量培养方法的开发

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摘要

Methylobacterium extorquens strains are the best-studied methylotrophic model system, and their metabolism of single carbon compounds has been studied for over 50 years. Here we develop a new system for high-throughput batch culture of M. extorquens in microtiter plates by jointly optimizing the properties of the organism, the growth media and the culturing system. After removing cellulose synthase genes in M. extorquens strains AM1 and PA1 to prevent biofilm formation, we found that currently available lab automation equipment, integrated and managed by open source software, makes possible reliable estimates of the exponential growth rate. Using this system, we developed an optimized growth medium for M. extorquens using response surface methodologies. We found that media that used EDTA as a metal chelator inhibited growth and led to inconsistent culture conditions. In contrast, the new medium we developed with a PIPES buffer and metals chelated by citrate allowed for fast and more consistent growth rates. This new Methylobacterium PIPES (‘MP’) medium was also robust to large deviations in its component ingredients which avoided batch effects from experiments that used media prepared at different times. MP medium allows for faster and more consistent growth than other media used for M. extorquens.
机译:甲基芽胞杆菌菌株是研究得最好的甲基营养模型系统,其对单个碳化合物的代谢研究已有50多年的历史了。在这里,我们通过共同优化生物体,生长培养基和培养系统的特性,开发了一种在微量滴定板中用于高通量分生克氏杆菌高通量分批培养的新系统。在去除了M. extorquens菌株AM1和PA1中的纤维素合酶基因以防止生物膜形成之后,我们发现由开放源码软件集成和管理的当前可用的实验室自动化设备,可以对指数增长率进行可靠的估计。使用该系统,我们使用响应面方法开发了一种最佳的拉克氏菌生长培养基。我们发现使用EDTA作为金属螯合剂的培养基会抑制生长,并导致不一致的培养条件。相反,我们开发的具有PIPES缓冲液和被柠檬酸盐螯合的金属的新培养基可以实现更快,更一致的生长速度。这种新的甲基杆菌PIPES('MP')培养基还具有强大的组成成分偏差,避免了使用在不同时间制备的培养基的实验产生的批量效应。 MP培养基比其他用于M. extorquens的培养基可以更快,更一致地生长。

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