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紫外线辐射对集胞藻PCC 6803细胞功能的影响及其在光合有效辐射下的恢复

Effects of ultraviolet radiation on cellular functions of the cyanobacterium Synechocystis sp. PCC 6803 and its recovery under photosynthetically active radiation.

作者信息

Singh Prashant R, Gupta Amit, Singh Ashish P, Jaiswal Jyoti, Sinha Rajeshwar P

机构信息

Laboratory of Photobiology and Molecular Microbiology, Department of Botany, Institute of Science, Banaras Hindu University, Varanasi 221005, India.

Laboratory of Photobiology and Molecular Microbiology, Department of Botany, Institute of Science, Banaras Hindu University, Varanasi 221005, India.

出版信息

J Photochem Photobiol B. 2024 Mar;252:112866. doi: 10.1016/j.jphotobiol.2024.112866. Epub 2024 Feb 9.

Abstract

Cyanobacteria are photosynthetic organisms and challenged by large number of stresses, especially by ultraviolet radiation (UVR). UVR primarily impacts lipids, proteins, DNA, photosynthetic performance, which lowers the fitness and production of cyanobacteria. UVR has a catastrophic effect on cyanobacterial cells and eventually leads to cell death. UVR tolerance in the Synechocystis was poorly studied. Therefore, we irradiated Synechocystis sp. PCC 6803 to varying hours of photosynthetically active radiations (PAR), PAR + UV-A (PA), and PAR + UV-A + UV-B (PAB) for 48 h. To study the tolerance of Synechocystis sp. PCC 6803 against different UVR. The study shows that Chl a and total carotenoids content increased up to 36 h in PAR and PA, after 36 h a decrease was observed. PC increased up to 4-fold in 48 h of PA irradiation compared to 12 h. Maximum increase in ROS was observed under 48 h PAB i.e., 5.8-fold. Flowcytometry (FCM) based analysis shows that 25% of cells do not give fluorescence of Chl a and HDCFH. In case of cell viability 10% cells were found to be non-viable in 48 h of PAB irradiance compared to 12 h. From the above study it was found that FCM-based approaches would provide a better understanding of the variations that occurred within the Synechocystis cells compared to fluorescence microscopy-based methods.

摘要

蓝藻是光合生物,面临着大量胁迫,尤其是紫外线辐射(UVR)。UVR主要影响脂质、蛋白质、DNA和光合性能,这会降低蓝藻的适应性和产量。UVR对蓝藻细胞具有灾难性影响,最终导致细胞死亡。对集胞藻中UVR耐受性的研究较少。因此,我们用不同时长的光合有效辐射(PAR)、PAR + UV - A(PA)和PAR + UV - A + UV - B(PAB)照射集胞藻PCC 6803 48小时。以研究集胞藻PCC 6803对不同UVR的耐受性。研究表明,在PAR和PA处理中,叶绿素a和总类胡萝卜素含量在36小时内增加,36小时后开始下降。与12小时相比,在PA照射48小时后藻蓝蛋白增加了4倍。在48小时PAB处理下观察到活性氧的最大增加,即增加了5.8倍。基于流式细胞术(FCM)的分析表明,25%的细胞不发出叶绿素a和二氯二氢荧光素的荧光。在细胞活力方面,与12小时相比,在48小时PAB照射下发现10%的细胞无活力。从上述研究发现,与基于荧光显微镜的方法相比,基于FCM的方法能更好地了解集胞藻细胞内发生的变化。

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