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Determination of Cell Doubling Times from the Return-on-Investment Time of Photosynthetic Vesicles based on Atomic Detail Structural Models

机译:基于原子细节结构模型的光合囊泡投资回报时间确定细胞倍增时间

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摘要

Cell doubling times of the purple bacterium Rhodobacter sphaeroides during photosynthetic growth are determined experimentally and computationally as a function of illumination. For this purpose, energy conversion processes in an intracytoplasmic membrane vesicle, the chromatophore, are described based on an atomic detail structural model. The cell doubling time and its illumination dependence are computed in terms of the return-on-investment (ROI) time of the chromatophore, determined computationally from the ATP production rate, and the mass ratio of chromatophores in the cell, determined experimentally from whole cell absorbance spectra. The ROI time is defined as the time it takes to produce enough ATP to pay for the construction of another chromatophore. The ROI time of the low light-growth chromatophore is 4.5–2.6 hours for a typical illumination range of 10–100 μmol photons m−2 s−1, respectively, with corresponding cell doubling times of 8.2–3.9 hours. When energy expenditure is considered as a currency, the benefit-to-cost ratio computed for the chromatophore as an energy harvesting device is 2–8 times greater than for photovoltaic and fossil fuel based energy solutions, whereas the corresponding ROI times are approximately 3–4 orders of magnitude shorter for the chromatophore than for synthetic systems.
机译:紫色细菌球形红细菌在光合作用生长过程中的细胞倍增时间是根据照明条件通过实验和计算确定的。为此目的,基于原子细节结构模型描述了细胞质内膜囊泡中的能量转化过程。细胞的倍增时间及其照度依赖性是根据由ATP产生速率计算得出的色谱的投资回报(ROI)时间以及由整个细胞实验得出的细胞中色谱的质量比来计算的吸收光谱。 ROI时间定义为产生足够的ATP来支付构建另一种色谱所需的时间。对于典型的10–100μmol光子m -2 s -1 的典型照射范围,低光生长色谱的ROI时间为4.5–2.6小时,相应的细胞倍增时间为8.2-3.9小时。如果将能源支出视为一种货币,则计算得出的作为能量收集装置的色谱的成本效益比是基于光伏和化石燃料的能源解决方案的2-8倍,而相应的ROI时间约为3-染色体比合成系统短4个数量级。

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