Biochar-immobilized Bacillus megaterium enhances Cd immobilization in soil and promotes Brassica chinensis growth.

Phosphate solubilizing bacteria (PSB) has been considered an environmental-friendly phosphate fertilizer without cadmium (Cd) input into soils, but its possibility of Cd fixation in soil needs to be explored. Since direct inoculation results in a rapid decline of the population and activity, we immobilized Bacillus megaterium with maize straw biochar (B-PSB) and investigated its feasibility in remediating Cd-contaminated soil. Pot experiments showed that the application of B-PSB significantly ameliorated the growth of Brassica chinensis under Cd stress, with a fresh weight increased by 59.08% compared to the Cd-control. B-PSB reduced Cd accumulation in Brassica chinensis by 61.69%, and promoted the uptake of P and N by 134.97% and 98.71% respectively. Microbial community analysis showed B-PSB recruited more plant growth-promoting bacteria in near-rhizosphere soil, which provides a favorable microenvironment for both PSB and crops. Column leaching experiments verified that B-PSB achieved the dissolution of stable P while fixing Cd. Batch tests further revealed that biochar served as a successful carrier facilitating the growth of B. megaterium and Cd immobilization. Given the widespread Cd contamination in agricultural soils, our results indicate that B-PSB is a promising soil amendment to secure food safety.

Stability and biomineralization of cadmium sulfide nanoparticles biosynthesized by the bacterium Rhodopseudomonas palustris under light.

Cadmium (Cd) pollution is regarded as a potent problem due to its hazard risks to the environment, making it crucial to be removed. Compared to the physicochemical techniques (e.g., adsorption, ion exchange, etc.), bioremediation is a promising alternative technology for Cd removal, due to its cost-effectiveness, and eco-friendliness. Among them, microbial-induced cadmium sulfide mineralization (Bio-CdS NPs) is a process of great significance for environmental protection. In this study, microbial cysteine desulfhydrase coupled with cysteine acted as a strategy for Bio-CdS NPs by Rhodopseudomonas palustris. The synthesis, activity, and stability of Bio-CdS NPs-R. palustris hybrid was explored under different light conditions. Results show that low light (LL) intensity could promote cysteine desulfhydrase activities to accelerate hybrid synthesis, and facilitated bacterial growth by the photo-induced electrons of Bio-CdS NPs. Additionally, the enhanced cysteine desulfhydrase activity effectively alleviated high Cd-stress. However, the hybrid rapidly dissolved under changed environmental factors, including light intensity and oxygen. The factors affecting the dissolution were ranked as follows: darkness/microaerobic ≈ darkness/aerobic < LL/microaerobic < high light (HL)/microaerobic < LL/aerobic < HL/aerobic. The research provides a deeper understanding of Bio-CdS NPs-bacteria hybird synthesis and its stability in Cd-polluted water, allowing advanced bioremediation treatment of heavy metal pollution in water.

Establishment of a resource recycling strategy by optimizing isobutanol production in engineered cyanobacteria using high salinity stress.

BACKGROUND: Isobutanol is an attractive biofuel with many advantages. Third-generation biorefineries that convert CO2 into bio-based fuels have drawn considerable attention due to their lower feedstock cost and more ecofriendly refining process. Although autotrophic cyanobacteria have been genetically modified for isobutanol biosynthesis, there is a lack of stable and convenient strategies to improve their production. RESULTS: In this study, we first engineered Synechococcus elongatus for isobutanol biosynthesis by introducing five exogenous enzymes, reaching a production titer of 0.126 g/L at day 20. It was then discovered that high salinity stress could result in a whopping fivefold increase in isobutanol production, with a maximal in-flask titer of 0.637 g/L at day 20. Metabolomics analysis revealed that high salinity stress substantially altered the metabolic profiles of the engineered S. elongatus. A major reason for the enhanced isobutanol production is the acceleration of lipid degradation under high salinity stress, which increases NADH. The NADH then participates in the engineered isobutanol-producing pathway. In addition, increased membrane permeability also contributed to the isobutanol production titer. A cultivation system was subsequently developed by mixing synthetic wastewater with seawater to grow the engineered cyanobacteria, reaching a similar isobutanol production titer as cultivation in the medium. CONCLUSIONS: High salinity stress on engineered cyanobacteria is a practical and feasible biotechnology to optimize isobutanol production. This biotechnology provides a cost-effective approach to biofuel production, and simultaneously recycles chemical nutrients from wastewater and seawater.

Selenium nanoparticles ameliorate Brassica napus L. cadmium toxicity by inhibiting the respiratory burst and scavenging reactive oxygen species.

Cadmium (Cd) is a widely distributed soil contaminant which induces oxidative damage and is therefore toxic to plants. Although selenium oxyanions such as selenite (SeO32-) and selenate (SeO42-) can alleviate Cd stress to plants, it is not known whether selenium nanoparticles (SeNPs) are able to do the same. The present study demonstrated the positive impact of both SeNPs and SeO32- on Brassica napus L. growth under conditions of Cd stress. Underlying mechanisms were elucidated using an oxidative stress detection assay, whole-genome RNA sequencing, and RT-qPCR. Application of selenium, especially in the form of SeNPs, decreased Cd-induced reactive oxygen species production by inhibiting the expression of NADPH oxidases (BnaRBOHC, BnaRBOHD1, and BnaRBOHF1) and glycolate oxidase (BnaGLO), thereby decreasing oxidative protein and membrane lipid damage. In addition, SeNPs improved resistance to Cd stress by decreasing Cd accumulation, maintaining intracellular calcium homeostasis, promoting disulfide bond formation, and restoring the waxy outer layer of the leaf surface. Although both forms of selenium decreased Cd toxicity, the beneficial concentration range was more extensive for SeNPs than for SeO32-.

D-amino acids inhibit initial bacterial adhesion: thermodynamic evidence.

Bacterial biofilms are structured communities of cells enclosed in a self-produced hydrated polymeric matrix that can adhere to inert or living surfaces. D-Amino acids were previously identified as self-produced compounds that mediate biofilm disassembly by causing the release of the protein component of the polymeric matrix. However, whether exogenous D-amino acids could inhibit initial bacterial adhesion is still unknown. Here, the effect of the exogenous amino acid D-tyrosine on initial bacterial adhesion was determined by combined use of chemical analysis, force spectroscopic measurement, and theoretical predictions. The surface thermodynamic theory demonstrated that the total interaction energy increased with more D-tyrosine, and the contribution of Lewis acid-base interactions relative to the change in the total interaction energy was much greater than the overall nonspecific interactions. Finally, atomic force microscopy analysis implied that the hydrogen bond numbers and adhesion forces decreased with the increase in D-tyrosine concentrations. D-Tyrosine contributed to the repulsive nature of the cell and ultimately led to the inhibition of bacterial adhesion. This study provides a new way to regulate biofilm formation by manipulating the contents of D-amino acids in natural or engineered systems.

Influences of D-tyrosine on the stability of activated sludge flocs.

The sludge floc stability is essential for the solid/liquid separation in biological wastewater treatment. In this study, the effect of an exogenous d-tyrosine on the shear stability and surface characteristics of activated sludge flocs was investigated. Sludge flocs were found to be less stable in the addition of d-tyrosine. d-Tyrosine inhibited the production of extracellular polymeric substances (EPS) especially for the proteins. A high correlation coefficient was observed between the composition of EPS fraction and d-tyrosine content. In addition, the hydrophobicity of sludge flocs was reduced and the zeta potential was more negative with the content of d-tyrosine increased. A linear relationship between the extracellular polymeric substances and surface characteristics for sludge flocs indicated that the inhibited EPS production may be responsible for the instability of sludge upon the addition of d-tyrosine.

Characterization of the interactions between tetracycline antibiotics and microbial extracellular polymeric substances with spectroscopic approaches.

The antibiotics have attracted global attentions for their impact on aquatic ecosystem. The knowledge about the fate of antibiotics encountering extracellular polymeric substances (EPS) is, however, limited. In this study, we investigated the interacting mechanisms of tetracycline (TC) to EPS extracted from aerobic activated sludge. The contributions of the main components of EPS, extracellular proteins, and polysaccharides were evaluated using bovine serum albumin and alginate sodium, respectively. Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and nuclear magnetic resonance indicated that hydroxyl, carboxyl, and amino groups were the domain chemical groups involved in the interaction between TC and EPS, and the binding of TC onto EPS changed the structure of these chemical groups, thus causing shifts in their UV-visible absorption spectra. In addition, we found that extracellular proteins, rather than polysaccharides, were the major active contents involved in the interaction. Three-dimensional excitation-emission matrix fluorescence spectroscopy showed that the fluorophores in EPS were clearly quenched by TC and the static quenching process was observed, implying the complex formation of TC and EPS. Furthermore, thermodynamic analysis indicated that the binding of TC with EPS is spontaneous and dominated by electrostatic forces.

Sorption and biodegradation of tetracycline by nitrifying granules and the toxicity of tetracycline on granules.

This paper examines the simultaneous sorption and biodegradation performance of tetracycline (TC) by the nitrifying granular sludge as well as the short-term exposure toxicity of TC. The removal of TC was characterized by a quick sorption and a slow process of biodegradation. The adsorption process fits pseudo-second-order kinetic model, with a complex mechanism of surface adsorption and intra-particle diffusion. Both temperature and mixed liquor suspended solid (MLSS) influenced TC sorption to the granules. TC biodegradation was enhanced with the increase of COD and NH(4)(+)-N concentrations, with except of the NH(4)(+)-N concentrations higher than 150 mg/L. With the ATU addition, TC degradation was weakened remarkably, indicating a synergistic effect of multiple microbes. Results of the short-term exposure (12h) effects showed that the respirometric activities of the microbes decreased greatly. The addition of TC also decreased the rate of NH(4)(+)-N utilization considerably, with the half saturation constant (K(s)) increasing from 297.7 to 347.2 mg/L.