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An equation for biomimicking macromolecular crowding using Escherichia coli MG1655 strain

机译:使用大肠杆菌MG1655菌株的生物剥削大分子挤出的等式

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Macromolecules present in the intracellular environment of a cell are densely packed, resulting in a highly crowded cytosolic environment. This crowded milieu influences several biochemical equilibria such as diffusibility and association constant of biomolecules which impose a serious impact on cellular functions as well as its processes. A number of in silico and in vitro studies have been reported till date about using synthetic crowding agents for resembling such a crowding environment within the cell. Lately, it has been realized that synthetic crowders are not suitable for mimicking the intrinsic environment of the cell. In this study, proteins were assumed to be the major biological molecule which contributes to the crowding environment. We have semi-theoretically determined the total protein concentration within an individual E. coli MG1655 cell which changes notably as the growth curve proceeds from 0.2 to 1.0 OD600. The average range of total cellular protein concentration throughout the batch culture was found to be in the range of 15.2 to 178?fg/fL of cytoplasmic volume. The fundamental knowledge gained through the study was translated to applied research in the form of an equation. We propose an equation that could help to mimic the OD600 dependent crowding environment present within a single cell of E. coli in the desired volume of reaction solution. In a nutshell, the equation provides quantitative estimation of the volume of culture required to prepare the cell lysate for biomimicking the intracellular crowding environment in vitro. This finding provides a new insight into the cellular cytosolic environment that could be used as a platform to frame more cells like environment in cell-free protein synthesis (CFPS) system for synthetic biology applications.
机译:存在于细胞的细胞内环境中的大分子密集包装,导致胞质环境高度拥挤。这种拥挤的Milieu影响了几种生化均衡,例如生物分子的扩散性和结合常数,这对细胞功能和过程产生了严重影响。迄今为止,使用合成拥挤剂在细胞内类似于这种拥挤的环境的综合拥挤剂,迄今为止,已经报道了许多在硅和体外研究。最近,已经意识到合成队员不适合模仿细胞的内在环境。在本研究中,假设蛋白质是有助于拥挤环境的主要生物分子。我们已经半理解了单独的大肠杆菌Mg1655细胞内的总蛋白质浓度,显着变化,因为生长曲线从0.2-1.000D600进行。发现整个分批培养物的平均细胞蛋白质浓度的平均范围在15.2至178℃的细胞质体积的范围内。通过该研究获得的基本知识被翻译成以方程式的形式应用研究。我们提出了一种方程,可以有助于模仿在所需的反应溶液中在大肠杆菌的单个细胞内存在的OD600依赖的拥挤环境。简而言之,该等式提供了制备细胞裂解物的培养物体积的定量估计,用于在体外进行生物剥削细胞内拥挤环境。该发现提供了一种新的洞察力,进入细胞细胞溶质环境,可以用作符合细胞蛋白质合成(CFPS)系统中的更多细胞的平台,用于合成生物学应用。

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