Abstract

Cyanobacteria use a carbon dioxide (CO2)-concentrating mechanism (CCM) that enhances their carbon fixation efficiency and is regulated by many environmental factors that impact photosynthesis, including carbon availability, light levels, and nutrient access. Efforts to connect the regulation of the CCM by these factors to functional effects on carbon assimilation rates have been complicated by the aqueous nature of cyanobacteria. Here, we describe the use of cyanobacteria in a semiwet state on glass fiber filtration discs-cyanobacterial discs-to establish dynamic carbon assimilation behavior using gas exchange analysis. In combination with quantitative PCR (qPCR) and transmission electron microscopy (TEM) analyses, we linked the regulation of CCM components to corresponding carbon assimilation behavior in the freshwater, filamentous cyanobacterium Fremyella diplosiphon Inorganic carbon (Ci) levels, light quantity, and light quality have all been shown to influence carbon assimilation behavior in F. diplosiphon Our results suggest a biphasic model of cyanobacterial carbon fixation. While behavior at low levels of CO2 is driven mainly by the Ci uptake ability of the cyanobacterium, at higher CO2 levels, carbon assimilation behavior is multifaceted and depends on Ci availability, carboxysome morphology, linear electron flow, and cell shape. Carbon response curves (CRCs) generated via gas exchange analysis enable rapid examination of CO2 assimilation behavior in cyanobacteria and can be used for cells grown under distinct conditions to provide insight into how CO2 assimilation correlates with the regulation of critical cellular functions, such as the environmental control of the CCM and downstream photosynthetic capacity.IMPORTANCE Environmental regulation of photosynthesis in cyanobacteria enhances organismal fitness, light capture, and associated carbon fixation under dynamic conditions. Concentration of carbon dioxide (CO2) near the carbon-fixing enzyme RubisCO occurs via the CO2-concentrating mechanism (CCM). The CCM is also tuned in response to carbon availability, light quality or levels, or nutrient access-cues that also impact photosynthesis. We adapted dynamic gas exchange methods generally used with plants to investigate environmental regulation of the CCM and carbon fixation capacity using glass fiber-filtered cells of the cyanobacterium Fremyella diplosiphon We describe a breakthrough in measuring real-time carbon uptake and associated assimilation capacity for cells grown in distinct conditions (i.e., light quality, light quantity, or carbon status). These measurements demonstrate that the CCM modulates carbon uptake and assimilation under low-Ci conditions and that light-dependent regulation of pigmentation, cell shape, and downstream stages of carbon fixation are critical for tuning carbon uptake and assimilation.

Highlights

  • Cyanobacteria use a carbon dioxide (CO2)-concentrating mechanism (CCM) that enhances their carbon fixation efficiency and is regulated by many environmental factors that impact photosynthesis, including carbon availability, light levels, and nutrient access

  • We hypothesized that identification of the conditions under which carbon assimilation was disrupted in WT F. diplosiphon or a ΔrcaE mutant strain with compromised chromatic acclimation (CCA) would highlight functional roles of CCA in impacting the regulation of CCM and associated carbon fixation and would indicate mechanisms for future analysis

  • The use of gas exchange analysis to construct Carbon response curves (CRCs) in cyanobacteria suggests that the acclimation to dominant light quality through CCA has a nuanced impact on overall assimilation behavior

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Summary

Introduction

Cyanobacteria use a carbon dioxide (CO2)-concentrating mechanism (CCM) that enhances their carbon fixation efficiency and is regulated by many environmental factors that impact photosynthesis, including carbon availability, light levels, and nutrient access. As the carbon fixation steps of photosynthesis are often regulated to ensure that they are kept in balance with the overall rate of photosynthesis [3], components of the CCM are likely to be tuned to environmental factors that affect photosynthesis, as well (Fig. 1) Both carbon transport and carboxysome components are upregulated under conditions where there is a greater need for Ci uptake and fixation, such as during growth under conditions of low CO2 or high light (HL) [4, 5]. A parallel set of proteins with higher substrate affinity can be induced to increase Ci uptake and includes SbtA, an inducible Naϩ/HCO3- symporter [10]; BCT1, an ATP-dependent HCO3- pump [11]; and NDH-13 (subunits D3/F3/CupA) at the thylakoid membrane [6, 8, 12] These complexes provide cyanobacteria with a high and tunable capacity for regulating internal Ci-influx as HCO3-. Other shell protein paralogs that may be found in carboxysomes include CcmK1, CcmK3, CcmK4, CcmK5, CcmK6, CcmO, CcmP, and CcmL [15, 20,21,22,23,24,25,26]

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