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单细胞蓝细菌蓝藻ATCC51142在昼夜明暗循环中的动态蛋白质组学分析。

Dynamic proteomic profiling of a unicellular cyanobacterium Cyanothece ATCC51142 across light-dark diurnal cycles.

作者信息

Aryal Uma K, Stöckel Jana, Krovvidi Ravi K, Gritsenko Marina A, Monroe Matthew E, Moore Ronald J, Koppenaal David W, Smith Richard D, Pakrasi Himadri B, Jacobs Jon M

机构信息

Pacific Northwest National Laboratory, Richland, WA 99352, USA.

出版信息

BMC Syst Biol. 2011 Dec 1;5:194. doi: 10.1186/1752-0509-5-194.

Abstract

BACKGROUND

Unicellular cyanobacteria of the genus Cyanothece are recognized for their ability to execute nitrogen (N2)-fixation in the dark and photosynthesis in the light. An understanding of these mechanistic processes in an integrated systems context should provide insights into how Cyanothece might be optimized for specialized environments and/or industrial purposes. Systems-wide dynamic proteomic profiling with mass spectrometry (MS) analysis should reveal fundamental insights into the control and regulation of these functions.

RESULTS

To expand upon the current knowledge of protein expression patterns in Cyanothece ATCC51142, we performed quantitative proteomic analysis using partial ("unsaturated") metabolic labeling and high mass accuracy LC-MS analysis. This dynamic proteomic profiling identified 721 actively synthesized proteins with significant temporal changes in expression throughout the light-dark cycles, of which 425 proteins matched with previously characterized cycling transcripts. The remaining 296 proteins contained a cluster of proteins uniquely involved in DNA replication and repair, protein degradation, tRNA synthesis and modification, transport and binding, and regulatory functions. Functional classification of labeled proteins suggested that proteins involved in respiration and glycogen metabolism showed increased expression in the dark cycle together with nitrogenase, suggesting that N2-fixation is mediated by higher respiration and glycogen metabolism. Results indicated that Cyanothece ATCC51142 might utilize alternative pathways for carbon (C) and nitrogen (N) acquisition, particularly, aspartic acid and glutamate as substrates of C and N, respectively. Utilization of phosphoketolase (PHK) pathway for the conversion of xylulose-5P to pyruvate and acetyl-P likely constitutes an alternative strategy to compensate higher ATP and NADPH demand.

CONCLUSION

This study provides a deeper systems level insight into how Cyanothece ATCC51142 modulates cellular functions to accommodate photosynthesis and N2-fixation within the single cell.

摘要

背景

蓝丝菌属的单细胞蓝细菌因其在黑暗中进行固氮作用以及在光照下进行光合作用的能力而受到认可。在综合系统背景下对这些机制过程的理解,应能为如何针对特定环境和/或工业目的优化蓝丝菌提供见解。通过质谱(MS)分析进行全系统动态蛋白质组学分析,应能揭示对这些功能的控制和调节的基本见解。

结果

为了扩展对蓝丝菌ATCC51142中蛋白质表达模式的现有认识,我们使用部分(“不饱和”)代谢标记和高质量精度液相色谱 - 质谱分析进行了定量蛋白质组学分析。这种动态蛋白质组学分析鉴定出721种在整个明暗周期中表达有显著时间变化的活跃合成蛋白质,其中425种蛋白质与先前表征的循环转录本相匹配。其余296种蛋白质包含一组独特参与DNA复制和修复、蛋白质降解、tRNA合成和修饰、转运和结合以及调节功能的蛋白质。标记蛋白质的功能分类表明,参与呼吸作用和糖原代谢的蛋白质与固氮酶一起在黑暗周期中表达增加,这表明固氮作用是由更高的呼吸作用和糖原代谢介导的。结果表明,蓝丝菌ATCC51142可能利用替代途径获取碳(C)和氮(N),特别是分别将天冬氨酸和谷氨酸作为C和N的底物。利用磷酸酮醇酶(PHK)途径将木酮糖 - 5P转化为丙酮酸和乙酰 - P可能构成一种替代策略,以补偿更高的ATP和NADPH需求。

结论

本研究提供了更深入的系统层面见解,以了解蓝丝菌ATCC51142如何调节细胞功能,以在单个细胞内适应光合作用和固氮作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87f1/3261843/4d721ae268cd/1752-0509-5-194-1.jpg

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