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从单个色素的体内特征重建集胞藻 PCC 6803 光突变体的吸收光谱。

Reconstruction of the absorption spectrum of Synechocystis sp. PCC 6803 optical mutants from the in vivo signature of individual pigments.

机构信息

Instituto de Aplicaciones de las Tecnologías de la Información y de las Comunicaciones Avanzadas, Universitat Politècnica de València, Valencia, Spain.

Department of Biophysics, Faculty of Science, Palacký University, Olomouc, Czech Republic.

出版信息

Photosynth Res. 2021 Jan;147(1):75-90. doi: 10.1007/s11120-020-00799-8. Epub 2020 Nov 27.

Abstract

In this work, we reconstructed the absorption spectrum of different Synechocystis sp. PCC 6803 optical strains by summing the computed signature of all pigments present in this organism. To do so, modifications to in vitro pigment spectra were first required: namely wavelength shift, curve smoothing, and the package effect calculation derived from high pigment densities were applied. As a result, we outlined a plausible shape for the in vivo absorption spectrum of each chromophore. These are flatter and slightly broader in physiological conditions yet the mean weight-specific absorption coefficient remains identical to the in vitro conditions. Moreover, we give an estimate of all pigment concentrations without applying spectrophotometric correlations, which are often prone to error. The computed cell spectrum reproduces in an accurate manner the experimental spectrum for all the studied wavelengths in the wild-type, Olive, and PAL strain. The gathered pigment concentrations are in agreement with reported values in literature. Moreover, different illumination set-ups were evaluated to calculate the mean absorption cross-section of each chromophore. Finally, a qualitative estimate of light-limited cellular growth at each wavelength is given. This investigation describes a novel way to approach the cell absorption spectrum and shows all its inherent potential for photosynthesis research.

摘要

在这项工作中,我们通过对该生物体内所有色素的计算特征进行求和,重建了不同的集胞藻 PCC 6803 光学品系的吸收光谱。为此,首先需要对体外色素光谱进行修正:即波长位移、曲线平滑以及从高色素密度衍生出的封装效应计算。结果,我们勾勒出了每个生色团的体内吸收光谱的合理形状。在生理条件下,这些光谱更平坦且略微变宽,但单位重量的平均吸收系数与体外条件保持一致。此外,我们还给出了所有色素浓度的估计值,而没有应用常易出错的分光光度相关法。所计算的细胞光谱在所有研究波长下都能准确地再现实验光谱,适用于野生型、橄榄型和 PAL 型菌株。所获得的色素浓度与文献中报道的值一致。此外,还评估了不同的照明设置,以计算每个生色团的平均吸收截面。最后,对每个波长的光限制细胞生长进行了定性估计。这项研究描述了一种新的方法来研究细胞吸收光谱,并展示了其在光合作用研究中的所有潜在用途。

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