Multi-Level, Multi Time-Scale Fluorescence Intermittency of Photosynthetic LH2 Complexes: A Precursor of Non-Photochemical Quenching?

2015 ◽  
Vol 119 (44) ◽  
pp. 13958-13963 ◽  
Author(s):  
Mario Schörner ◽  
Sebastian Reinhardt Beyer ◽  
June Southall ◽  
Richard J. Cogdell ◽  
Jürgen Köhler
Keyword(s):  
Time Scale ◽  
Photochemical Quenching ◽  
Multi Level ◽  
Non Photochemical Quenching ◽  
Fluorescence Intermittency

Light Absorption and Partitioning in Response to Nitrogen in Apple Leaves

HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 541a-541
Author(s):  
Lailiang Cheng ◽  
Leslie H. Fuchigami ◽  
Patrick J. Breen
Keyword(s):  
High Light ◽  
Thermal Dissipation ◽  
Photochemical Quenching ◽  
Light Conditions ◽  
Psii Efficiency ◽  
Fluorescence Measurements ◽  
Free Radical Formation ◽  
Highly Correlated ◽  
Non Photochemical Quenching ◽  
Leaf N

Bench-grafted Fuji/M26 apple trees were fertigated with different concentrations of nitrogen by using a modified Hoagland solution for 6 weeks, resulting in a range of leaf N from 1.0 to 4.3 g·m–2. Over this range, leaf absorptance increased curvilinearly from 75% to 92.5%. Under high light conditions (1500 (mol·m–2·s–1), the amount of absorbed light in excess of that required to saturate CO2 assimilation decreased with increasing leaf N. Chlorophyll fluorescence measurements revealed that the maximum photosystem II (PSII) efficiency of dark-adapted leaves was relatively constant over the leaf N range except for a slight drop at the lower end. As leaf N increased, non-photochemical quenching under high light declined and there was a corresponding increase in the efficiency with which the absorbed photons were delivered to open PSII centers. Photochemical quenching coefficient decreased significantly at the lower end of the leaf N range. Actual PSII efficiency increased curvilinearly with increasing leaf N, and was highly correlated with light-saturated CO2 assimilation. The fraction of absorbed light potentially used for free radical formation was estimated to be about 10% regardless of the leaf N status. It was concluded that increased thermal dissipation protected leaves from photo-oxidation as leaf N declined.

scholarly journals Gradual Response of Cyanobacterial Thylakoids to Acute High-Light Stress—Importance of Carotenoid Accumulation

Cells ◽  
2021 ◽  
Vol 10 (8) ◽  
pp. 1916
Author(s):  
Myriam Canonico ◽  
Grzegorz Konert ◽  
Aurélie Crepin ◽  
Barbora Šedivá ◽  
Radek Kaňa
Keyword(s):  
Single Cell ◽  
Thylakoid Membrane ◽  
Intermediate Phase ◽  
Light Stress ◽  
Fast Response ◽  
High Light ◽  
Photochemical Quenching ◽  
Second Phase ◽  
Ros Scavenging ◽  
Non Photochemical Quenching

Light plays an essential role in photosynthesis; however, its excess can cause damage to cellular components. Photosynthetic organisms thus developed a set of photoprotective mechanisms (e.g., non-photochemical quenching, photoinhibition) that can be studied by a classic biochemical and biophysical methods in cell suspension. Here, we combined these bulk methods with single-cell identification of microdomains in thylakoid membrane during high-light (HL) stress. We used Synechocystis sp. PCC 6803 cells with YFP tagged photosystem I. The single-cell data pointed to a three-phase response of cells to acute HL stress. We defined: (1) fast response phase (0–30 min), (2) intermediate phase (30–120 min), and (3) slow acclimation phase (120–360 min). During the first phase, cyanobacterial cells activated photoprotective mechanisms such as photoinhibition and non-photochemical quenching. Later on (during the second phase), we temporarily observed functional decoupling of phycobilisomes and sustained monomerization of photosystem II dimer. Simultaneously, cells also initiated accumulation of carotenoids, especially ɣ–carotene, the main precursor of all carotenoids. In the last phase, in addition to ɣ-carotene, we also observed accumulation of myxoxanthophyll and more even spatial distribution of photosystems and phycobilisomes between microdomains. We suggest that the overall carotenoid increase during HL stress could be involved either in the direct photoprotection (e.g., in ROS scavenging) and/or could play an additional role in maintaining optimal distribution of photosystems in thylakoid membrane to attain efficient photoprotection.

scholarly journals The Role of Acidic Residues in the C Terminal Tail of the LHCSR3 Protein of Chlamydomonas reinhardtii in Non-Photochemical Quenching

2021 ◽  
pp. 6895-6900
Author(s):  
Franco V. A. Camargo ◽  
Federico Perozeni ◽  
Gabriel de la Cruz Valbuena ◽  
Luca Zuliani ◽  
Samim Sardar ◽  
...  
Keyword(s):  
Chlamydomonas Reinhardtii ◽  
Photochemical Quenching ◽  
Acidic Residues ◽  
Non Photochemical Quenching

scholarly journals Effects of iron limitation on carbon balance and photophysiology of the Antarctic diatom Chaetoceros cf. simplex

Polar Biology ◽  
2021 ◽  
Author(s):  
Deborah Bozzato ◽  
Torsten Jakob ◽  
Christian Wilhelm ◽  
Scarlett Trimborn
Keyword(s):  
Oxygen Evolution ◽  
Photochemical Quenching ◽  
Gross Photosynthesis ◽  
Manganese Zinc ◽  
C Cycle ◽  
Uptake Rates ◽  
Carbon Pump ◽  
Non Photochemical Quenching ◽  
The Antarctic ◽  
Biological Carbon Pump

AbstractIn the Southern Ocean (SO), iron (Fe) limitation strongly inhibits phytoplankton growth and generally decreases their primary productivity. Diatoms are a key component in the carbon (C) cycle, by taking up large amounts of anthropogenic CO2 through the biological carbon pump. In this study, we investigated the effects of Fe availability (no Fe and 4 nM FeCl3 addition) on the physiology of Chaetoceros cf. simplex, an ecologically relevant SO diatom. Our results are the first combining oxygen evolution and uptake rates with particulate organic carbon (POC) build up, pigments, photophysiological parameters and intracellular trace metal (TM) quotas in an Fe-deficient Antarctic diatom. Decreases in both oxygen evolution (through photosynthesis, P) and uptake (respiration, R) coincided with a lowered growth rate of Fe-deficient cells. In addition, cells displayed reduced electron transport rates (ETR) and chlorophyll a (Chla) content, resulting in reduced cellular POC formation. Interestingly, no differences were observed in non-photochemical quenching (NPQ) or in the ratio of gross photosynthesis to respiration (GP:R). Furthermore, TM quotas were measured, which represent an important and rarely quantified parameter in previous studies. Cellular quotas of manganese, zinc, cobalt and copper remained unchanged while Fe quotas of Fe-deficient cells were reduced by 60% compared with High Fe cells. Based on our data, Fe-deficient Chaetoceros cf. simplex cells were able to efficiently acclimate to low Fe conditions, reducing their intracellular Fe concentrations, the number of functional reaction centers of photosystem II (RCII) and photosynthetic rates, thus avoiding light absorption rather than dissipating the energy through NPQ. Our results demonstrate how Chaetoceros cf. simplex can adapt their physiology to lowered assimilatory metabolism by decreasing respiratory losses.

Non-photochemical quenching in epipsammic and epipelic microalgal assemblages from two marine ecosystems

2017 ◽  
Vol 136 ◽  
pp. 74-82 ◽  
Author(s):  
Filip F. Pniewski ◽  
Pierre Richard ◽  
Adam Latała ◽  
Gerard Blanchard
Keyword(s):  
Marine Ecosystems ◽  
Photochemical Quenching ◽  
Non Photochemical Quenching

Non-photochemical quenching of chlorophyll a fluorescence: early history and characterization of two xanthophyll-cycle mutants of Chlamydomonas reinhardtii

2002 ◽  
Vol 29 (10) ◽  
pp. 1141 ◽  
Author(s):  
Govindjee ◽  
Manfredo J. Seufferheld
Keyword(s):  
Chlamydomonas Reinhardtii ◽  
Oxygen Evolution ◽  
Xanthophyll Cycle ◽  
Photochemical Quenching ◽  
Chl A ◽  
Fluorescence Transient ◽  
Chl A Fluorescence ◽  
Non Photochemical Quenching

This paper deals first with the early, although incomplete, history of photoinhibition, of 'non-QA-related chlorophyll (Chl) a fluorescence changes', and the xanthophyll cycle that preceded the discovery of the correlation between non-photochemical quenching of Chl a fluorescence (NPQ) and conversion of violaxanthin to zeaxanthin. It includes the crucial observation that the fluorescence intensity quenching, when plants are exposed to excess light, is indeed due to a change in the quantum yield of fluorescence. The history ends with a novel turn in the direction of research — isolation and characterization of NPQ xanthophyll-cycle mutants of Chlamydomonas reinhardtii Dangeard and Arabidopsis thaliana (L.) Heynh., blocked in conversion of violaxanthin to zeaxanthin, and zeaxanthin to violaxanthin, respectively. In the second part of the paper, we extend the characterization of two of these mutants (npq1, which accumulates violaxanthin, and npq2, which accumulates zeaxanthin) through parallel measurements on growth, and several assays of PSII function: oxygen evolution, Chl a fluorescence transient (the Kautsky effect), the two-electron gate function of PSII, the back reactions around PSII, and measurements of NPQ by pulse-amplitude modulation (PAM 2000) fluorimeter. We show that, in the npq2 mutant, Chl a fluorescence is quenched both in the absence and presence of 3-(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU). However, no differences are observed in functioning of the electron-acceptor side of PSII — both the two-electron gate and the back reactions are unchanged. In addition, the role of protons in fluorescence quenching during the 'P-to-S' fluorescence transient was confirmed by the effect of nigericin in decreasing this quenching effect. Also, the absence of zeaxanthin in the npq1 mutant leads to reduced oxygen evolution at high light intensity, suggesting another protective role of this carotenoid. The available data not only support the current model of NPQ that includes roles for both pH and the xanthophylls, but also are consistent with additional protective roles of zeaxanthin. However, this paper emphasizes that we still lack sufficient understanding of the different parts of NPQ, and that the precise mechanisms of photoprotection in the alga Chlamydomonas may not be the same as those in higher plants.

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