Abstract

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

Highlights

  • Unicellular cyanobacteria of the genus Cyanothece are recognized for their ability to execute nitrogen (N2)-fixation in the dark and photosynthesis in the light

  • Based on the quantitative information of new protein synthesis, we provided an overview of the temporal separation of cellular processes and metabolism in Cyanothece ATCC51142 during the light-dark cycle

  • Interrogation of the dynamic proteome over two consecutive diurnal cycles provided a unique picture of real-time protein synthesis in response to the lightdark cycle

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Summary

Introduction

Unicellular cyanobacteria of the genus Cyanothece are recognized for their ability to execute nitrogen (N2)-fixation in the dark and photosynthesis in the light. Oxygenic photosynthetic cyanobacteria are widely recognized for their important role in the global carbon cycle [1], and have generated significant interest as a potential solution for carbon-neutral energy production and carbon (C) sequestration [2] Some unicellular cyanobacteria such as Cyanothece and Crocosphaera are capable of biological N2-fixation (diazotrophic) [3], and play a significant role in marine nitrogen (N) cycle [4]. Cyanothece have developed mechanisms to switch/alternate the cellular and molecular machinery twice daily to temporally separate N2-fixation in the dark from photosynthesis in the light [6,7] Components of this temporal segregation of incompatible metabolic functions are controlled by circadian rhythms and/or daily oscillations of bio-chemicals in response to the light-dark cycle [8]. Cellular metabolism in various cyanobacteria is intricately linked to and modified by growth conditions that include lighting regimes [11]

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