The Phycobihproteids in Cyanophora paradoxa as Accessoric Pigments and Nitrogen Storage Proteins

1983 ◽  
Vol 38 (11-12) ◽  
pp. 972-977 ◽  
Author(s):  
Hainfried E. A. Schenk ◽  
Jürgen Hanf ◽  
Margarete Neu-Müller
Keyword(s):  
Electron Transport ◽  
Stress Proteins ◽  
Nitrogen Starvation ◽  
Storage Proteins ◽  
Photosynthetic Electron Transport ◽  
Lower Degree ◽  
Nitrogen Storage ◽  
Cyanophora Paradoxa ◽  
Free Living

The phycobiliproteids of cyanobacteria have two functions. They are accessoric pigments for the light-dependent photosynthetic electron transport, and, secondly, they are storage proteins. Cyanocyta korschikoffiana, the endocyanelle of Cyanophora paradoxa, a hardly adapted endocytobiotic cyanobacterium, is responsible for the photoautotrophy of the host flagellate. The biosynthesis of the phycobiliproteids takes place in the endocyanelles and is reversible. Under nitrogen starvation the phycobiliproteids were disintegrated again, in contrast to the carotenoids (and in a lower degree to chlorophyll), whose contents rem ain more constant in the cells, as shown by in vivo measurements. Therefore, it is concluded that sim ilar to the function in free living cyanobacteria the phycobiliproteids of C. paradoxa also serve as storage substances (“stress proteins”). This opinion is supported by experiments with chloramphenicol

Metribuzin-Resistant Mutants of Chlamydomonas reinhardii

1984 ◽  
Vol 39 (5) ◽  
pp. 437-439 ◽  
Author(s):  
N. Pucheu ◽  
W. Oettmeier ◽  
U. Heisterkamp ◽  
K. Masson ◽  
G.F. Wildner
Keyword(s):  
Electron Transport ◽  
Photosynthetic Electron Transport ◽  
Wild Type ◽  
Binding Studies ◽  
Molecular Weight Range ◽  
Chlamydomonas Reinhardii ◽  
Thylakoid Membrane Proteins ◽  
Mutant Strains ◽  
Resistant Mutants

Herbicide resistance in Chlamydomonas reinhardii cells was induced by mutagenesis with 5-fluorodeoxyuridine and ethylmethanesulfonate. Four mutant strains were isolated and analyzed for resistance against DCMU-type or phenolic inhibitors of photosynthetic electron transport. The mutants were different in both the extent and the pattern of their resistance: the R/S value, i.e. the ratio of I50 values of the inhibition of photosynthetic electron transport in isolated resistant and susceptible thylakoids, varied for metribuzin from 10 000 to 36. The mutant MZ-1 was resistant against metribuzin, atrazine and DCMU, whereas the mutant MZ-2 showed resistance mainly against metribuzin and atrazine. The mutant MZ-3 was similar to MZ-1, but showed a lesser extent of resistance against DCMU. The mutant MZ-4 showed resistance against metribuzin, but not against atrazine. These results demonstrate that the resistance against one herbicide of the DCMU-type (metribuzin) must not be accompanied by similar resistance against te other inhibitors. Binding studies with radioactively labeled herbicides, [14C]metribuzin, [14C]atrazine and [3H]DCMU, and isolated thylakoids supported these observations. Phosphorylation of thylakoid membrane proteins was studied with wild-type cells and resistant mutants under in vivo conditions in the light. The 32P-labeled main proteins bands were in the molecular weight range of 10-14 kDa, 26-29 kDa, 32-35 kDa and 46-48 kDa. The pattern and the extent of incorporation of 32P were similar for the mutants and the wild-type cells.

On the Mechanism of Benzoquinone Penetration and Photoreduction by Whole Cells

1971 ◽  
Vol 26 (6) ◽  
pp. 585-588 ◽  
Author(s):  
H. Gimmler ◽  
M. Avron
Keyword(s):  
Electron Transport ◽  
Cell Membrane ◽  
Photosynthetic Electron Transport ◽  
Electron Acceptors ◽  
Electron Donors ◽  
Porphyridium Cruentum ◽  
Whole Cells ◽  
Time Treatment ◽  
Short Time

Short time treatment of intact Porphyridium cruentum cells with benzoquinone results in changes of the cell membranes, which lead to a higher permeability. This increased permeability allows the measurements of photosynthetic electron transport reactions with various electron donors, ac. ceptors and mediators, which cannot enter untreated cells. The capacity of benzoquinone to act as a Hill - reagent in vivo is interpreted as due to a double action of this compound: changing the permeability of the cells by reacting with the cell membrane coupled with the ability of the unreacted molecules to serve as electron acceptors.

Multiple in vivo Effects of Cadmium on Photosynthetic Electron Transport in Pea Plants

2021 ◽  
Author(s):  
Daria Todorenko ◽  
Alena Volgusheva ◽  
Nyurgun Timofeev ◽  
Ilya Kovalenko ◽  
Dmitry Matorin ◽  
...  
Keyword(s):  
Electron Transport ◽  
Photosynthetic Electron Transport ◽  
In Vivo Effects

Research note: Energy partitioning in photosystem II complexes subjected to photoinhibitory treatment

2007 ◽  
Vol 34 (3) ◽  
pp. 214 ◽  
Author(s):  
Dmytro Kornyeyev ◽  
Luke Hendrickson
Keyword(s):  
Electron Transport ◽  
Photosystem Ii ◽  
Excitation Energy ◽  
Chlorophyll A ◽  
Chlorophyll A Fluorescence ◽  
Photosynthetic Electron Transport ◽  
Energy Partitioning ◽  
Simple Equations

Chlorophyll a fluorescence measured in vivo is frequently used to study the role of different processes influencing the distribution of excitation energy in PSII complexes. Such studies are important for understanding the regulation of photosynthetic electron transport. However, at the present time, there is no unified methodology to analyse the energy partitioning in PSII. In this article, we critically assess several approaches recently developed in this area of research and propose new simple equations, which can be used for de-convolution of non-photochemical energy quenching in PSII complexes.

Irreversibly Binding Photosynthetic Electron Transport Inhibitors II. Halogen-Substituted 1,4-Naphthoquinones and Halogenmethyl-1,4-quinones

1987 ◽  
Vol 42 (6) ◽  
pp. 693-697 ◽  
Author(s):  
Walter Oettmeier ◽  
Ralf Dostatni ◽  
Hans-Joachim Santel
Keyword(s):  
Electron Transport ◽  
Photosystem Ii ◽  
Binding Affinity ◽  
Alkylating Agents ◽  
Photosynthetic Electron Transport ◽  
Hydrogen Halide ◽  
Covalent Linkage ◽  
Transport Inhibitors ◽  
Preincubation Time

Several halogen-substituted 1,4-naphthoquinones have been synthesized and found to be effective photosystem II inhibitors. Due to their properties as vinylogous acid halides they can react with nucleophiles under formation of a covalent linkage. In their presence other photosystem II herbicides show a decreased binding affinity. This decrease is dependent from the preincubation time. Halogenmethyl-1,4-quinones also turned out to be efficient photosystem II inhibitors and. in addition, possessed herbicidal in vivo activity. They function as “bioreductive alkylating agents” in a way that after reduction they can split off hydrogen halide under formation of a o-quinonemethide. This quinonemethide can react with nucleophilic groups in proteins.

Changes in Photosynthetic Electron Transport during Leaf Senescence in Two Barley Varieties Grown in Contrasting Growth Regimes

2020 ◽  
Vol 61 (11) ◽  
pp. 1986-1994 ◽  
Author(s):  
Ginga Shimakawa ◽  
Thomas Roach ◽  
Anja Krieger-Liszkay
Keyword(s):  
Electron Transport ◽  
Leaf Senescence ◽  
Near Infrared ◽  
Electron Paramagnetic Resonance Spectroscopy ◽  
Photosynthetic Electron Transport ◽  
Growth Conditions ◽  
Significant Loss ◽  
Resonance Spectroscopy ◽  
Ros Production

Abstract Leaf senescence is an important process for plants to remobilize a variety of metabolites and nutrients to sink tissues, such as developing leaves, fruits and seeds. It has been suggested that reactive oxygen species (ROS) play an important role in the initiation of leaf senescence. Flag leaves of two different barley varieties, cv. Lomerit and cv. Carina, showed differences in the loss of photosystems and in the production of ROS at a late stage of senescence after significant loss of chlorophyll (Krieger-Liszkay et al. 2015). Here, we investigated photosynthetic electron transport and ROS production in primary leaves of these two varieties at earlier stages of senescence. Comparisons were made between plants grown outside in natural light and temperatures and plants grown in temperature-controlled growth chambers under low light intensity. Alterations in the content of photoactive P700, ferredoxin and plastocyanin (PC) photosynthetic electron transport were analyzed using in vivo near-infrared absorbance changes and chlorophyll fluorescence, while ROS were measured with spin-trapping electron paramagnetic resonance spectroscopy. Differences in ROS production between the two varieties were only observed in outdoor plants, whereas a loss of PC was common in both barley varieties regardless of growth conditions. We conclude that the loss of PC is the earliest detectable photosynthetic parameter of leaf senescence while differences in the production of individual ROS species occur later and depend on environmental factors.

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