Evidence map›Paper›PMID 25915422›Full record

ArticlePloS one2015

Photosynthetic Membranes of Synechocystis or Plants Convert Sunlight to Photocurrent through Different Pathways due to Different Architectures.

Roy I Pinhassi, Dan Kallmann, Gadiel Saper, Shirley Larom, Artyom Linkov, Alix Boulouis, Mark-Aurel Schöttler, Ralph Bock, Avner Rothschild, Noam Adir and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.6field-weighted citation impact, top 31% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
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  3. Article
  4. Direct Electricity Production fromInternational journal of molecular sciences · 2022
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  6. Review
  7. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 2 countries.

Roy I PinhassiGrand Technion Energy Program, Technion-Israel Institute of Technology, Technion City, Haifa 32000 Israel; Faculty of Biology, Technion-Israel Institute of Technology, Technion City, Haifa 32000 Israel; Schulich Faculty of Chemistry, Technion-Israel Institute of Technology, Technion City, Haifa 32000 Israel; Department of Science and Material Engineering, Technion-Israel Institute of Technology, Technion City, Haifa 32000 Israel.
Dan KallmannGrand Technion Energy Program, Technion-Israel Institute of Technology, Technion City, Haifa 32000 Israel; Faculty of Biology, Technion-Israel Institute of Technology, Technion City, Haifa 32000 Israel; Schulich Faculty of Chemistry, Technion-Israel Institute of Technology, Technion City, Haifa 32000 Israel; Department of Science and Material Engineering, Technion-Israel Institute of Technology, Technion City, Haifa 32000 Israel.
Gadiel SaperGrand Technion Energy Program, Technion-Israel Institute of Technology, Technion City, Haifa 32000 Israel; Faculty of Biology, Technion-Israel Institute of Technology, Technion City, Haifa 32000 Israel; Schulich Faculty of Chemistry, Technion-Israel Institute of Technology, Technion City, Haifa 32000 Israel; Department of Science and Material Engineering, Technion-Israel Institute of Technology, Technion City, Haifa 32000 Israel.
Shirley LaromFaculty of Biology, Technion-Israel Institute of Technology, Technion City, Haifa 32000 Israel.
Artyom LinkovSchulich Faculty of Chemistry, Technion-Israel Institute of Technology, Technion City, Haifa 32000 Israel.
Alix BoulouisMax-Planck-Institut für molekulare Pflanzenphysiologie, Am Mühlenberg 1, D-14476 Potsdam-Golm, Germany.
Mark-Aurel SchöttlerMax-Planck-Institut für molekulare Pflanzenphysiologie, Am Mühlenberg 1, D-14476 Potsdam-Golm, Germany.
Ralph BockMax-Planck-Institut für molekulare Pflanzenphysiologie, Am Mühlenberg 1, D-14476 Potsdam-Golm, Germany.
Avner RothschildGrand Technion Energy Program, Technion-Israel Institute of Technology, Technion City, Haifa 32000 Israel; Department of Science and Material Engineering, Technion-Israel Institute of Technology, Technion City, Haifa 32000 Israel.
Noam AdirGrand Technion Energy Program, Technion-Israel Institute of Technology, Technion City, Haifa 32000 Israel; Schulich Faculty of Chemistry, Technion-Israel Institute of Technology, Technion City, Haifa 32000 Israel.
Gadi SchusterGrand Technion Energy Program, Technion-Israel Institute of Technology, Technion City, Haifa 32000 Israel; Faculty of Biology, Technion-Israel Institute of Technology, Technion City, Haifa 32000 Israel.
Technion – Israel Institute of Technology · ILMax Planck Institute of Molecular Plant Physiology · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Thylakoid membranes contain the redox active complexes catalyzing the light-dependent reactions of photosynthesis in cyanobacteria, algae and plants. Crude thylakoid membranes or purified photosystems from different organisms have previously been utilized for generation of electrical power and/or fuels. Here we investigate the electron transferability from thylakoid preparations from plants or the cyanobacterium Synechocystis. We show that upon illumination, crude Synechocystis thylakoids can reduce cytochrome c. In addition, this crude preparation can transfer electrons to a graphite electrode, producing an unmediated photocurrent of 15 μA/cm2. Photocurrent could be obtained in the presence of the PSII inhibitor DCMU, indicating that the source of electrons is QA, the primary Photosystem II acceptor. In contrast, thylakoids purified from plants could not reduce cyt c, nor produced a photocurrent in the photocell in the presence of DCMU. The production of significant photocurrent (100 μA/cm2) from plant thylakoids required the addition of the soluble electron mediator DCBQ. Furthermore, we demonstrate that use of crude thylakoids from the D1-K238E mutant in Synechocystis resulted in improved electron transferability, increasing the direct photocurrent to 35 μA/cm2. Applying the analogous mutation to tobacco plants did not achieve an equivalent effect. While electron abstraction from crude thylakoids of cyanobacteria or plants is feasible, we conclude that the site of the abstraction of the electrons from the thylakoids, the architecture of the thylakoid preparations influence the site of the electron abstraction, as well as the transfer pathway to the electrode. This dictates the use of different strategies for production of sustainable electrical current from photosynthetic thylakoid membranes of cyanobacteria or higher plants.

Indexed as

ElectrodesElectronsElectron TransportLightPhotosynthesisPhotosystem II Protein ComplexSunlightSynechocystisThylakoidsPhotosystem II Protein Complex

Identifiers

PMID25915422
PMCPMC4411099
OpenAlexW2022646494

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.