Bio-hydrogen-producing Potential Evaluation and Capacity Enhancement from Tobacco Processing Leftovers by Photo-fermentation Under Diverse Initial pH.

The use of tobacco growing and processing residues for bio-hydrogen production is an effective exploration to broaden the source of bio-hydrogen production raw materials and realize waste recycling. In this study, bio-hydrogen-producing potential was evaluated and the effect of diverse initial pH on hydrogen production performance was investigated. The cumulative hydrogen yield (CHY) and the properties of fermentation liquid were monitored. The modified Gompertz model was adopted to analyze the kinetic characteristics of photo-fermentation bio-hydrogen production process. Results showed that CHY increased firstly and then decreased with the increase of initial pH. Highest CHY and hydrogen production rate of appeared at the initial pH of 8, which were 257.7 mL and 6.15 mL/h, respectively. The acidic initial pH was found to severely limit the bio-hydrogen production capacity. The correlation coefficients (R2) of hydrogen production kinetics parameters were all greater than 0.99, meaning that the fitting effect was good. The main metabolites of bacteria in the system were acetic acid, butyric acid, and ethanol, and the consumption of acetic acid was promoted with the increase of initial pH.

S(-II) reactivates Cd2+-stressed Shewanella oneidensis via promoting low-molecular-weight thiols synthesis and activating antioxidant defense.

Efficient remedies for living organisms including bacteria to counteract cadmium (Cd2+) toxicity are still highly needed. Plant toxicity studies have showed that exogenous S(-II) (including hydrogen sulfide and its ionic forms, i.e., H2S, HS-, and S2-) application can effectively alleviate adverse effects of Cd stress, but whether S(-II) could mitigate bacterial Cd toxicity remains unclear. In this study, S(-II) was applied exogenously to Cd-stressed Shewanella oneidensis MR-1 and the results showed that S(-II) can significantly reactivate impaired physiological processes including growth arrest and enzymatic ferric (Fe(III) reduction inhibition. The efficacy of S(-II) treatment is negatively correlated with the concentration and time length of Cd exposure. Energy-dispersive X-ray (EDX) analysis suggested the presence of cadmium sulfide inside cells treated with S(-II). Both compared proteomic analysis and RT-qPCR showed that enzymes associated with sulfate transport, sulfur assimilation, methionine, and glutathione biosynthesis were up-regulated in both mRNA and protein levels after the treatment, indicating S(-II) may induce the biosynthesis of functional low-molecular-weight (LMW) thiols to counteract Cd toxicity. Meanwhile, the antioxidant enzymes were positively modulated by S(-II) and thus the activity of intracellular reactive oxygen species was attenuated. The study demonstrated that exogenous S(-II) can effectively alleviate Cd stress for S. oneidensis likely through inducing intracellular trapping mechanisms and modulating cellular redox status. It suggested that S(-II) may be a highly effective remedy for bacteria such as S. oneidensis under Cd-polluted environments.

Transcriptome analysis of low-temperature-affected ripening revealed MYB transcription factors-mediated regulatory network in banana fruit.

Low temperature leads to abnormal ripening and poor quality of the harvested banana fruit, which is an urgent problem limiting the development of industry in China. To comprehensively understand the mechanism underlying low-temperature-affected ripening, we performed comparative RNA-Seq analysis of ethylene-induced ripening of banana fruit after 3 days of pre-storage at 7 °C and 22 °C. A total of 986 differentially expressed genes (DEGs) were identified in both RT-0 d versus RT-3 d, LT-0 d versus LT-3 d, RT-0 d versus LT-0 d and RT-3 d versus LT-3 d, and the RNA-Seq outputs of 15 randomly selective DEGs were verified using qRT-PCR. Among the 986 DEGs obtained in the four groups, 9 MYB genes (MaMYB75/281/219/4/151/156/3/37 and MaMYB3R1) and 32 genes related to carotenoid biosynthesis (MaPSY1/2a), flavor formation (MaLOX6, MaADH7, MaAAT1), sucrose transport (MaSUS2/4), ethylene production (MaSAM1, MaACO9/10/12, MaACS1/12), starch degradation (MaAMY1A/1B, MaPHS1/2, MaMEX2, MapGlcT1) and cell wall degradation (MaPG3/X1, MaPME25/41, MaXTH5/7/22/23/25, MaEXP2/20/A1/A15) were characterized. Combining transcription factor binding site (TFBS) analysis as well as cis-acting element analysis, the regulatory network of low-temperature-affected ripening mediated by MYBs were constructed. The data generated in this study may unravel the transcriptional regulatory network of MYBs associated with low-temperature-affected ripening and provide a solid foundation for future studies.

Fate of oxalic-acid-intervened arsenic during Fe(II)-induced transformation of As(V)-bearing jarosite.

Jarosite is a metastable Fe(III)-oxyhydroxysulfate mineral that can act as an excellent scavenger for arsenic (As) in acid sulfate soils (ASSs) and in areas polluted by acid mine drainage (AMD). The Fe(II)-induced transformation of jarosite can influence the As mobility in reducing soil and sediment systems. Although organic acids are prevalent in these environments, their influence on the behavior of As during the Fe(II)-induced transformation of jarosite is yet to be fully understood. In this study, we investigated the effects of oxalic acid on the partitioning of As into dissolved, adsorbed, poorly crystalline, and residual phases during the Fe(II)-induced transformation of As(V)-bearing jarosite at pH 5.5 and 1 mM Fe(II) concentration. The results demonstrated that jarosite frequently transformed to lepidocrocite in treatments without oxalic acid or with low oxalic acid (0.1 mM), and As was typically redistributed in the surface-bound exchangeable and residual phases. While a high concentration of oxalic acid (1 mM) retarded the transformation of jarosite and produced goethite as the primary end product, it also changed the Fe(II)-induced transformation pathway and drove most As into the residual phase (approximately 92%). The results indicated that oxalic acid exerts a significant influence on the partitioning and speciation of As during the above-mentioned transformation. X-ray photo electron spectroscopy analysis of the reaction products also revealed that As(V) may be still the dominant redox species. Overall, this study provides critical information for understanding the fate of As during the transformation of secondary minerals under complex influencing factors, thereby assisting in more accurately predicting the geochemical cycling of As in natural systems.

Reductive dissolution of jarosite by a sulfate reducing bacterial community: Secondary mineralization and microflora development.

Jarosite is an iron-hydroxysulfate mineral commonly found in acid mine drainage (AMD). Given its strong adsorption capacity and its ability to co-precipitation with heavy metals, jarosite is considered a potent scavenger of contaminants in AMD-impacted environments. Sulfate-reducing bacteria (SRB) play an important role in the reductive dissolution of jarosite; however, the mechanism involved has yet to be elucidated. In this study, an indigenous SRB community enriched from the Dabaoshan mine area (Guangdong, China) was employed to explore the mechanism of the microbial reduction of jarosite. Different cultures, with or without dissolved sulfate and the physical separation of jarosite from bacteria by dialysis bags, were examined. Results indicate that the reduction of jarosite by SRB occurred via an indirect mechanism. In systems with dissolved sulfate, lactate was incompletely oxidized to acetate coupled with the reduction of SO42- to S2-, which subsequently reduced the Fe3+ in jarosite, forming secondary minerals including vivianite, mackinawite and pyrite. In systems without dissolved sulfate, jarosite dissolution occurred prior to reduction, and similar secondary minerals formed as well. Extracellular polymeric substances secreted by SRB appeared to facilitate the release of sulfate from jarosite. Structural sulfate in the solid phase of jarosite may not be available for SRB respiration. Although direct contact between SRB and jarosite is not necessary for mineral reduction, wrapping jarosite into dialysis bags suppressed the reduction to a certain extent. Microbial community composition differed in direct contact treatments and physical separation treatments. Physical separation of the SRB community from jarosite mineral supported the growth of Citrobacter, while Desulfosporosinus dominated in direct contact treatments.