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Green hydrogen, produced during microalgal photosynthesis, is regarded as one of the most promising sustainable energy sources. It utilizes sunlight and water, which are essentially unlimited, and its combustion results in only water as a waste product. In microalgal hydrogen energy production systems, the sensitivity of hydrogenase to O2 poses a significant challenge, limiting sustained photosynthetic H2 production in microalgae. Additionally, efficient photosynthetic H2 production in anaerobic microalgal cells is hindered by impaired electron source (photosystem II) and electron loss through the Calvin‐Benson cycle, cyclic electron transfer around photosystem I, and O2 photoreduction, which are identified as the other key challenges. Over the past eight decades, considerable progress has been made in addressing these challenges and regulating electron transfer to achieve sustainable and efficient photosynthetic H2 production in microalgae. In this review, we discuss a range of regulatory methods for achieving sustainable and efficient photosynthetic H2 production in microalgae. Emphasizing the significant progress made over the past eight decades, we also address current challenges and propose potential future solutions. [ABSTRACT FROM AUTHOR]

Background: Bisulfite addition is an important H2 photoproduction strategy that removes O2 and activates hydrogenase. The pH values of cell cultures can change the ratio of bisulfite to sulfite, which may affect H2 photoproduction. However, little is known regarding the pH effect of bisulfite addition on H2 photoproduction and relevant underlying mechanism. Results: Here, changes in H2 photoproduction with different initial extracellular pH values showed a parabolic distribution and a pH of 8.0 is an optimal value for H2 photoproduction in Chlamydomonas reinhardtii cells treated with bisulfite. Compared to the growth pH (pH 7.3), increased photoproduction of H2 at this optimal pH was primarily caused by a relatively high residual activity of photosystem II (PSII), which provides a relatively plentiful source of electrons for H2 photoproduction. Such increased H2 photoproduction was most likely a result of decreased the ratio of bisulfite to sulfite, consistent with the result that the toxicity of bisulfite on PSII was much more than that of sulfite. This possibility was corroborated by the result that treatment with a combination of 7 mM bisulfite and 6 mM sulfite further enhanced H2 photoproduction compared with 13 mM bisulfite alone. Conclusions: Collectively, our findings provide novel mechanistic insights into pH-dependent H2 photoproduction in C. reinhardtii cells treated with bisulfite, and demonstrate that sulfite addition is another important strategy for H2 photoproduction, just like bisulfite addition. [ABSTRACT FROM AUTHOR]

Highlights: [•] A simple approach to produce H2 from Taihu Lake Microcystis spp. blooms is described. [•] Efficient H2 production occurred in the dark and was inactivated by light. [•] Efficient H2 production resulted from reduced O2 content and enhanced H2ase activity. [•] A post-treatment strategy is proposed to turn algal bloom waste into useful products. [ABSTRACT FROM AUTHOR]

Cyanobacterial NADPH:plastoquinone oxidoreductase, or type I NAD(P)H dehydrogenase, or the NDH-1 complex is involved in plastoquinone reduction and cyclic electron transfer (CET) around photosystem I. CET, in turn, produces extra ATP for cell metabolism particularly under stressful conditions. Despite significant achievements in the study of cyanobacterial NDH-1 complexes during the past few years, the entire subunit composition still remains elusive. To identify missing subunits, we screened a transposon-tagged library of Synechocystis 6803 cells grown under high light. Two NDH-1-mediated CET (NDH-CET)-defective mutants were tagged in the same ssl0352 gene encoding a short unknown protein. To clarify the function of Ssl0352, the ssl0352 deletion mutant and another mutant with Ssl0352 fused to yellow fluorescent protein (YFP) and the His6 tag were constructed. Immunoblotting, mass spectrometry, and confocal microscopy analyses revealed that the Ssl0352 protein resides in the thylakoid membrane and associates with the NDH-1L and NDH-1M complexes. We conclude that Ssl0352 is a novel subunit of cyanobacterial NDH-1 complexes and designate it NdhS. Deletion of the ssl0352 gene considerably impaired the NDH-CET activity and also retarded cell growth under high light conditions, indicating that NdhS is essential for efficient operation of NDH-CET. However, the assembly of the NDH-1L and NDH-1M complexes and their content in the cells were not affected in the mutant. NdhS contains a Src homology 3-like domain and might be involved in interaction of the NDH-1 complex with an electron donor. [ABSTRACT FROM AUTHOR]

The mechanisms of acclimating to a nitrogen-fluctuating environment are necessary for the survival of aquatic cyanobacteria in their natural habitats, but our understanding is still far from complete. Here, the synthesis of phycobiliprotein is confirmed to be much earlier than that of photosystem components during recovery from nitrogen chlorosis and an unknown protein Ssr1698 is discovered to be involved in this synthetic process. The unknown protein is further identified as a c-type heme oxygenase (cHO) in tetrapyrrole biosynthetic pathway and catalyzes the opening of heme ring to form biliverdin IXα, which is required for phycobilin production and ensuing phycobiliprotein synthesis. In addition, the cHO-dependent phycobiliprotein is found to be vital for the growth of cyanobacterial cells during chlorosis and regreening through its nitrogen-storage and light-harvesting functions, respectively. Collectively, the cHO expressed preferentially during recovery from nitrogen chlorosis is identified in photosynthetic organisms and the dual function of this enzyme-dependent phycobiliprotein is proposed to be an important mechanism for acclimation of aquatic cyanobacteria to a nitrogen-fluctuating environment. Cyanobacterial Ssr1698 is a c-type heme oxygenase (cHO) and is involved in phycobiliprotein (PBP) biosynthesis. This cHO-dependent PBP is vital for adapting to nitrogen fluctuations through its nitrogen-storage and light-harvesting functions. [ABSTRACT FROM AUTHOR]

[Display omitted] • Bisulfite-induced cell growth inhibition reduces iron requirement. • Iron accumulation in bisulfite-treated cells results from reduced iron demand. • Accumulated iron enhances the Fenton reaction, leading to the disruption of PSII. • Iron deficiency suppresses the Fenton reaction and alleviates PSII impairment. • Iron deficiency boosts H 2 photoproduction in bisulfite-treated Chlamydomonas cells. Adding bisulfite is a significant strategy to enhance H 2 photoproduction, but it adversely affects photosystem II (PSII) activity in microalgae, consequently limiting H 2 production. Nevertheless, the exact mechanism through which bisulfite disrupts PSII remains unclear. Here, the addition of NaHSO 3 to Chlamydomonas reinhardtii cultures suppresses growth by inducing iron poisoning through the Fenton reaction, driven by reduced iron demand and the resultant accumulation of iron. Consequently, the removal of iron from C. reinhardtii cultures eliminates the iron poisoning triggered by the Fenton reaction. This, in turn, mitigates PSII impairment and leads to a significant increase in photosynthetic H 2 production in C. reinhardtii cells. Collectively, these discoveries unveil the precise mechanism by which bisulfite disrupts PSII, opening up a new avenue for substantially enhancing green hydrogen production from microalgae through the bisulfite addition strategy. [ABSTRACT FROM AUTHOR]

Abstract: In cyanobacteria, treatment with low concentrations of NaHSO3 can enhance photosynthetic efficiency, whereas NaHSO3 in high amounts often inhibits cell growth and photosynthesis may even cause death. In the present study, our results showed that treatment with moderate concentrations of NaHSO3 considerably improved the yield of photobiological H2 production in the filamentous N2-fixing cyanobacterium Anabaena sp. strain PCC 7120. Under steady state conditions, the accumulated H2 levels in cells treated with 1 mM NaHSO3 were approximately 10 times higher than that in untreated cells. Such improvement occurred in heterocysts and was most likely caused by increases in the expression and activity of nitrogenase. The effects of treatment with low, moderate, and high concentrations of NaHSO3 in cyanobacteria were proposed on the basis of the results obtained in the present study and from previous knowledge. [ABSTRACT FROM AUTHOR]

Abstract: In cyanobacteria, the light-harvesting complex phycobilisomes (PBS) can transfer the harvested energy to photosystem II (PSII) and photosystem I (PSI) and from PSII to PSI. The efficiency of energy transfer from PBS to PSII or PSI, as probed by the ratio of the fluorescence yield of PBS to that of PSII or PSI, was similar in static and aerated cultures of a cyanobacterium Synechocystis sp. strain PCC 6803. In contrast, the fluorescence yield for PSII was notably high while that for PSI was remarkably low in static cultures when compared to that in aerated cultures. Additionally, the level of the efficiency of excitation energy capture by open PSII reaction center was markedly decreased in static cultures in comparison to that in aerated cultures. Thus, the energy transfer from PSII to PSI, but not from PBS to PSII and PSI, was inhibited in static cultures and was most likely caused by the reduction of PSII activity. [Copyright &y& Elsevier]

Purpose: We sought to evaluate the performance of a new "one-stop-shop" scan protocol combining brain computed tomography perfusion (CTP) and head-and-neck CT angiography (CTA) imaging for acute stroke patients using a 256-detector CT scanner.Method: From March to August 2020, 60 patients (30 men and 30 women) aged 22-88 years with suspected acute stroke were enrolled and randomly divided into 2 groups to undergo brain CTP and head-and-neck CTA with a 256-detector CT system. Group A used traditional scan protocol with a separate brain CTP and head-and-neck CT examination that included non-contrast-enhanced and contrast-enhanced acquisitions; group B used the new "one-stop-shop" scan protocol with head-and-neck CTA data inserted into brain CTP scans at the peak time (PT) of the arterial phase. The insertion point of the head-and-neck CTA data was determined by a test bolus. The examination time, contrast dose, radiation dose, and image quality were compared between the groups.Results: The total contrast dose was reduced by 40% in group B compared to group A (60 mL vs. 100 mL). The imaging time was 52.5 ± 2.6 s in group B and 74.9 ± 3.3 s in group A, showing a reduction of approximately 43% in group B. There was no significant difference in image quality both quantitatively and qualitatively between the groups (all P > 0.05). Group B had a slight reduction in dose length product (1139.0 ± 45.3 vs. 1211.6 ± 31.9 mGy·cm, P < 0.001).Conclusions: The proposed "one-stop-shop" scan protocol combining brain CTP and head-and-neck CTA on a 256-detector CT system can reduce imaging time and contrast dose, without affecting image quality or perfusion results, compared to the traditional protocol of separating the examinations. [ABSTRACT FROM AUTHOR]

Abstract: Treatment with NaHSO3 induces a 10-fold increase in H2 photoproduction in the filamentous N2-fixing cyanobacterium Anabaena sp. strain PCC 7120. However, it is unclear whether this treatment also increases H2 photoproduction in green alga. In this study, treatment with 13mM NaHSO3 resulted in about a 200-fold increase in H2 production in Chlamydomonas reinhardtii, and this increase was most probably the result of reduced O2 content and enhanced hydrogenase activity. Compared to the conventional strategy of sulfur deprivation, NaHSO3 treatment results in a higher maximum rate of H2 photoproduction, greater efficiency of conversion of light energy into H2, shorter half-time to produce the maximum accumulated H2 levels, and reduced costs because no centrifugation is involved. We therefore conclude that NaHSO3 treatment is an efficient, rapid, and economic strategy for improving photobiological H2 production in the green alga C. reinhardtii. [Copyright &y& Elsevier]