Biology subjects

Adir, N.

Publications and source records attributed to Adir, N..

6 recordsLinked to original sources

bioRxiv2022

A desert green alga that thrives at extreme high-light intensities using a unique photoin-hibition protection mechanism

While light is the driving force of photosynthesis, excessive light can be harmful. Photoinhibition, or light-induced photo-damage, is one of the key processes limiting photosynthesis. When the absorbed light exceeds the amount that can be dissipated by photosynthetic electron flow and other processes, damaging radicals are formed that mostly inactivate photosystem II (PSII). A well-defined mechanism that protects the photosynthetic apparatus from photoinhibition has been described in the model green alga Chlamydomonas reinhardtii and plants. Chlorella oha-dii is a green micro-alga, isolated from biological desert soil crusts, that thrives under extreme high light (HL) in which other organisms do not survive. Here, we show that this alga evolved unique protection mechanisms distinct from those of C. reinhardtii and plants. When grown under extreme HL, significant structural changes were noted in the C. ohadii thylakoids, including a drastic reduction in the antennae and the formation of stripped core PSII, lacking its outer and inner antennae. This is accompanied by a massive accumulation of protective carotenoids and proteins that scavenge harmful radicals. At the same time, several elements central to photoinhibition protection in C. reinhardtii, such as psbS, the stress-related light harvesting complex, PSII protein phosphorylation and state-transitions are entirely absent or were barely detected in C. ohadii. Taken together, a unique photoinhibition protection mechanism evolved in C. ohadii, enabling the species to thrive under extreme-light intensities where other photo-synthetic organisms fail to survive.

plant biology↗

bioRxiv2022

Trichodesmium Erythraeum produces a higher photocurrent than other cyanobacterial species in bio-photo electrochemical cells.

In recent years, the increase in world energy consumption, and the worries from potential future disasters that may derive from climate change have inspired the motivation to develop renewable energy technologies. One of the promising methods is the utilization of whole bacterial cells to produce photocurrent in a bio-photo electrochemical cell (BPEC). The photocurrent derives from the photosynthesis pathway, while the redox couple NADP+/NADPH perform cyclic electron mediation between photosystem I inside the cells, and the anode. Over the years, various cyanobacterial species were utilized in diverse BPECs setups, while the photocurrent was enhanced by the addition of natural electron mediators such as NAD+, NADP+, Cytochrome C, Vitamin B1, and the artificial mediator potassium ferricyanide. The cyanobacterium Trichodesmium Erythraeum (Te) is a marine species that consist of high content of Phycocyanin and Phycoerythrin pigments that play a major role in photosynthesis enhancement. In this work, we produce for the first-time photocurrent from Te. We apply 2D-fluorescence measurements to detect its NADPH secretion and show that its photocurrent production is enhanced as a function of increasing electrolyte salinity. Finally, we produce photocurrent from additional cyanobacterial species: Synechocystis sp. PCC6803, Synechococcus elongatus PCC 7942, Acaryochloris marina MBIC 11017, and Spirulina, using their cultivation medium as electrolytes in the BPEC. We show that TE produces a photocurrent intensity that is significantly greater than all other species with and without the addition of exogenous electron mediators. The utilization of TE may pave the way toward the establishment of marine clean energy technologies.

microbiology↗

bioRxiv2021

A new replication medium enables a rapid identification of {varphi}x-174 virus by synchronous fluorescence of Tryptophan.

Development of rapid methods for detection of virus particles based on their intrinsic fluorescence is challenging. Pure viruses may be detected in filtered solutions, based on the strong fluorescence of the amino acid Tryptophan (Trp) in their proteins. Nevertheless, Trp also exists in high quantities in the hosts and host cultivation media. In this work, we show that a separation of the bacteriophage{varphi} x-174 from its E. coli host (grown on the standard cultivation medium "Nutrient Agar") by simple extraction and filtration is not sufficient for its detection based on the intrinsic fluorescence since ~70 % of the Trp fluorescence is derived from impurities. We formulate a new cultivation medium with very low Trp concentration. We apply synchronous fluorescence measurements to show that no Trp fluorescence is detected in the extract solution upon incubation of this medium substrate with ammonium acetate extraction buffer. Finally, we detect{varphi} x-174 based on the spectral fingerprint of its intrinsic Trp content by synchronous fluorescence measurements. The concept of coupling intrinsic fluorescence-based methods to impurities reduction in the source, may pave the way towards future development of simple, cheap, and rapid methods for detection of viral pathogens.

microbiology↗

bioRxiv2021

Harvesting electrical current from intact plant leaves

Here, we show that it is possible to harvest photocurrent directly from unprocessed plant tissues from terrestrial or aquatic environments in bio-photoelectrochemical cells (BPECs) and use the current to produce molecular H2. The source of electrons is shown to originate from the Photosystem II water-oxidation reaction and utilizes exported mediating molecules, especially NADPH. The photocurrent production is dependent on the concentration of the photosynthetic complexes, as an increase in total chlorophyll and oxygen evolution rates lead to increased photocurrent rates. The permeability of the outer leaf surface is another important factor in photocurrent harvesting. Different tissues produce photocurrent densities in the range of [~] 1 - 10 mA / cm2 which is significantly higher than microorganism-based BPECs. The relatively high photocurrent and the simplicity of the plants BPEC may pave the way toward the development of future applicative photosynthetic based energy technologies.

bioengineering↗

bioRxiv2021

Bioelectricity generation from live marine photosynthetic macroalgae

Conversion of solar energy into electrical current by photosynthetic organisms has the potential to produce clean energy. Previously reported bio-photoelectrochemical cells (BPECs) have utilized unicellular photosynthetic microorganisms. In this study, we describe for the first time BPECs that utilize intact live marine macroalgae (seaweeds) in natural seawater or saline buffer or natural seawater. The BPECs produce electrical currents from of >50mA/cm2, from both light-dependent (photosynthesis) and light independent processes. These values are significantly greater than the current densities that have been reported for single-cell microorganisms. The photocurrent is inhibited by the Photosystem II inhibitor DCMU, indicating that the source of light-driven electrons is from water oxidation via NADPH and other reduced molecules. We show here that intact seaweed cultures can be used in a large-scale BPEC containing seawater that produces bias-free photocurrent. The ability to produce bioelectricity from intact seaweeds may pave the way to future development of a low-cost energy technology using BPECs.

bioengineering↗

bioRxiv2021

The desert green algae Chlorella ohadii thrives at excessive high light intensities by exceptionally enhancing the mechanisms that protect photosynthesis from photoinhibition

Although light is the driving force of photosynthesis, excessive light can be harmful. One of the main processes that limits photosynthesis is photoinhibition, the process of light-induced photodamage. When the absorbed light exceeds the amount that is dissipated by photosynthetic electron flow and other processes, damaging radicals are formed that mostly inactivate photosystem II (PSII). Damaged PSII must be replaced by a newly repaired complex in order to preserve full photosynthetic activity. Chlorella ohadii is a green micro-alga, isolated from biological desert soil crusts, that thrives under extreme high light and is highly resistant to photoinhibition. Therefore, C. ohadii is an ideal model for studying the molecular mechanisms underlying protection against photoinhibition. Comparison of the thylakoids of C. ohadii cells that were grown under low light versus extreme high light intensities, found that the alga employs all three known photoinhibition protection mechanisms: i) massive reduction of the PSII antenna size; ii) accumulation of protective carotenoids; and iii) very rapid repair of photo-damaged reaction center proteins. This work elucidated the molecular mechanisms of photoinhibition resistance in one of the most light-tolerant photosynthetic organisms and shows how photoinhibition protection mechanisms evolved to marginal conditions, enabling photosynthesis-dependent life in severe habitats. One Sentence HighlightAnalysis of the photosynthetic properties of a desert algae that thrives at extreme high light intensities revealed protection from photoinhibition driven by the remarkable enhancement of three protection mechanisms.

plant biology↗