Biodegradation of Polystyrene by Pseudomonas sp. Isolated from the Gut of Superworms

Author(s):  
Hong Rae Kim ◽  
Hyun Min Lee ◽  
Eunbeen Jeon ◽  
Hee Cheol Yu ◽  
Sukkyoo Lee ◽  
...  

<p>Large quantities of plastic waste represent a grave social issue. Various attempts have been made to solve plastic waste problems, such as methods of natural plastic degradation. Currently, polystyrene (PS) is one of the most widely used plastics in many industries; therefore, degrading PS becomes a critical global issue. In this study, we isolated <i>Pseudomonas</i> sp., a strain of plastic-degrading bacteria known to survive only in the soil, from the gut of the superworms. Thus far, the degradation of PS by <i>Pseudomonas</i> sp. has barely been explored. We examined PS degradation using electronic microscopy, and measured changes in atomic distribution and contact angles with water droplets on the PS surface that represent a chemical change from hydrophobicity to hydrophilicity. During the process of PS degradation by <i>Pseudomonas</i> sp., we examined chemical structural changes using X-ray photoelectron spectroscopy (XPS), Fourier transform-infrared spectroscopy (FT-IR) and nuclear magnetic resonance spectroscopy (NMR) to check for the formation of C=O bonds and changes towards hydrophilicity. RT-qPCR was used to measure the gene expression level of <a></a><a>serine hydrolase </a>in <i>Pseudomonas</i>, an enzyme that mediates the plastic degradation. Our findings indicate that <i>Pseudomonas</i> present in the gut of the superworms participates in the degradation of plastics following ingestion. Moreover, this study also identified a candidate enzyme related to PS degradation in <i>Pseudomonas</i> for the first time. Thus, the findings of this study prove significance not only in presenting a novel function of <i>Pseudomonas</i> in the gut of superworms, but also in highlighting a potential solution for PS degradation.<b></b></p>

2019 ◽  
Author(s):  
Hong Rae Kim ◽  
Hyun Min Lee ◽  
Eunbeen Jeon ◽  
Hee Cheol Yu ◽  
Sukkyoo Lee ◽  
...  

<p>Large quantities of plastic waste represent a grave social issue. Various attempts have been made to solve plastic waste problems, such as methods of natural plastic degradation. Currently, polystyrene (PS) is one of the most widely used plastics in many industries; therefore, degrading PS becomes a critical global issue. In this study, we isolated <i>Pseudomonas</i> sp., a strain of plastic-degrading bacteria known to survive only in the soil, from the gut of the superworms. Thus far, the degradation of PS by <i>Pseudomonas</i> sp. has barely been explored. We examined PS degradation using electronic microscopy, and measured changes in atomic distribution and contact angles with water droplets on the PS surface that represent a chemical change from hydrophobicity to hydrophilicity. During the process of PS degradation by <i>Pseudomonas</i> sp., we examined chemical structural changes using X-ray photoelectron spectroscopy (XPS), Fourier transform-infrared spectroscopy (FT-IR) and nuclear magnetic resonance spectroscopy (NMR) to check for the formation of C=O bonds and changes towards hydrophilicity. RT-qPCR was used to measure the gene expression level of <a></a><a>serine hydrolase </a>in <i>Pseudomonas</i>, an enzyme that mediates the plastic degradation. Our findings indicate that <i>Pseudomonas</i> present in the gut of the superworms participates in the degradation of plastics following ingestion. Moreover, this study also identified a candidate enzyme related to PS degradation in <i>Pseudomonas</i> for the first time. Thus, the findings of this study prove significance not only in presenting a novel function of <i>Pseudomonas</i> in the gut of superworms, but also in highlighting a potential solution for PS degradation.<b></b></p>


Author(s):  
Shan Jiang ◽  
Tingting Su ◽  
Jingjing Zhao ◽  
Zhanyong Wang

Polystyrene (PS) is a widely used petroleum-based plastic, that pollutes the environment because it is difficult to degrade. In this study, a PS degrading bacterium identified as Massilia sp. FS1903 was successfully isolated from the gut of Galleria mellonella (Lepidoptera: Pyralidae) larvae that were fed with PS foam. Scanning electron microscopy and X-ray energy dispersive spectrometry showed that the structure and morphology of the PS film was destroyed by FS 1903, and that more oxygen appeared on the degraded PS film. A water contact angle assay verified the chemical change of the PS film from initially hydrophobic to hydrophilic after degradation. X-ray photoelectron spectroscopy further demonstrated that more oxygen-containing functional groups were generated during PS degradation. After 30 days of bacterial stain incubation with 0.15 g PS, 80 ml MSM, 30°C and PS of Mn 64400 and Mw 144400 Da, the weight of the PS film significantly decreased, with 12.97 ± 1.05% weight loss. This amount of degradation exceeds or is comparable to that previously reported for other species of bacteria reported to degrade PS. These results show that Massilia sp. FS1903 can potentially be used to degrade PS waste.


2021 ◽  
Vol 30 ◽  
pp. 2633366X2097865
Author(s):  
Li Jian

The surface treatment of carbon fibers (CFs) was carried out using a self-synthesized sizing agent. The effects of sizing agent on the surface of CFs and the interface properties of CF/polymethyl methacrylate (PMMA) composites were mainly studied. Scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and static contact angle were used to compare and study the CFs before and after the surface treatment, including surface morphology, surface chemical element composition, and wettability of the surface. The influence of sizing agent on the mechanical properties of CF/PMMA resin composite interface was investigated. The results show that after sizing treatment, the CF surface O/C value increased by 35.1% and the contact angles of CF and resin decreased by 16.2%. The interfacial shear strength and interlayer shear strength increased by 12.6%.


Nanomaterials ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 1519
Author(s):  
Jong Gyeong Kim ◽  
Sunghoon Han ◽  
Chanho Pak

The price and scarcity of platinum has driven up the demand for non-precious metal catalysts such as Fe-N-C. In this study, the effects of phosphoric acid (PA) activation and phosphorus doping were investigated using Fe-N-C catalysts prepared using SBA-15 as a sacrificial template. The physical and structural changes caused by the addition of PA were analyzed by nitrogen adsorption/desorption and X-ray diffraction. Analysis of the electronic states of Fe, N, and P were conducted by X-ray photoelectron spectroscopy. The amount and size of micropores varied depending on the PA content, with changes in pore structure observed using 0.066 g of PA. The electronic states of Fe and N did not change significantly after treatment with PA, and P was mainly found in states bonded to oxygen or carbon. When 0.135 g of PA was introduced per 1 g of silica, a catalytic activity which was increased slightly by 10 mV at −3 mA/cm2 was observed. A change in Fe-N-C stability was also observed through the introduction of PA.


2020 ◽  
Vol 6 (1) ◽  
pp. 34-49
Author(s):  
Abul Arafat ◽  
Sabrin A. Samad ◽  
Jeremy J. Titman ◽  
Andrew L. Lewis ◽  
Emma R. Barney ◽  
...  

AbstractThis study investigates the role of yttrium in phosphate-based glasses in the system 45(P2O5)–25(CaO)– (30-x)(Na2O)–x(Y2O3) (0≤x≤5) prepared via melt quenching and focuses on their structural characterisation and degradation properties. The structural analyses were performed using a combination of solid-state nuclear magnetic resonance (NMR), Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). 31P NMR analysis showed that depolymerisation of the phosphate network occurred which increased with Y2O3 content as metaphosphate units (Q2) decreased with subsequent increase in pyrophosphate species (Q1). The NMR results correlated well with structural changes observed via FTIR and XPS analyses. XRD analysis of crystallised glass samples revealed the presence of calcium pyrophosphate (Ca2P2O7) and sodium metaphosphate (NaPO3) phases for all the glass formulations explored. Yttrium-containing phases were found for the formulations containing 3 and 5 mol% Y2O3. Degradation analyses performed in Phosphate buffer saline (PBS) and Milli-Q water revealed significantly reduced rates with addition of Y2O3 content. This decrease was attributed to the formation of Y-O-P bonds where the octahedral structure of yttrium (YO6) cross-linked phosphate chains, subsequently leading to an increase in chemical durability of the glasses. The ion release studies also showed good correlation with the degradation profiles.


Polymers ◽  
2019 ◽  
Vol 11 (12) ◽  
pp. 1915 ◽  
Author(s):  
Eyob Wondu ◽  
Hyun Woo Oh ◽  
Jooheon Kim

In this study water-soluble polyurethane (WSPU) was synthesized from isophorone diisocyanate (IPDI), and polyethylene glycol (PEG), 2-bis(hydroxymethyl) propionic acid or dimethylolpropionic acid (DMPA), butane-1,4-diol (BD), and triethylamine (TEA) using an acetone process. The water solubility was investigated by solubilizing the polymer in water and measuring the contact angle and the results indicated that water solubility and contact angle tendency were increased as the molecular weight of the soft segment decreased, the amount of emulsifier was increased, and soft segment to hard segment ratio was lower. The contact angle of samples without emulsifier was greater than 87°, while that of with emulsifier was less than 67°, indicating a shift from highly hydrophobic to hydrophilic. The WSPU was also analyzed using Fourier transform infrared spectroscopy (FT-IR) to identify the absorption of functional groups and further checked by X-ray photoelectron spectroscopy (XPS). The molecular weight of WSPU was measured using size-exclusion chromatography (SEC). The structure of the WSPU was confirmed by nuclear magnetic resonance spectroscopy (NMR). The thermal properties of WSPU were analyzed using thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC).


Nanomaterials ◽  
2019 ◽  
Vol 9 (5) ◽  
pp. 706 ◽  
Author(s):  
Chaoqun Wu ◽  
Yudan Zhou ◽  
Haitao Wang ◽  
Jianhua Hu

Zwitterionic polymers are suitable for replacing poly(ethylene glycol) (PEG) polymers because of their better antifouling properties, but zwitterionic polymers have poor mechanical properties, strong water absorption, and their homopolymers should not be used directly. To solve these problems, a reversible-addition fragmentation chain transfer (RAFT) polymerization process was used to prepare copolymers comprised of zwitterionic side chains that were attached to an ITO glass substrate using spin-casting. The presence of 4-vinylpyridine (4VP) and zwitterion chains on these polymer-coated ITO surfaces was confirmed using 1H NMR, FTIR, and GPC analyses, with successful surface functionalization confirmed using water contact angle, X-ray photoelectron spectroscopy (XPS), and atomic force microscopy (AFM) studies. Changes in water contact angles and C/O ratios (XPS) analysis demonstrated that the functionalization of these polymers with β-propiolactone resulted in hydrophilic mixed 4VP/zwitterionic polymers. Protein adsorption and cell attachment assays were used to optimize the ratio of the zwitterionic component to maximize the antifouling properties of the polymer brush surface. This work demonstrated that the antifouling surface coatings could be readily prepared using a “P4VP-modified” method, that is, the functionality of P4VP to modify the prepared zwitterionic polymer. We believe these materials are likely to be useful for the preparation of biomaterials for biosensing and diagnostic applications.


2012 ◽  
Vol 482-484 ◽  
pp. 1585-1591 ◽  
Author(s):  
Cheng Fu Yang ◽  
Wei Wen Wang ◽  
Hsin Hwa Chen ◽  
Wei Tan Sun ◽  
Chi Lin Shiau ◽  
...  

In this paper, we report a new phenomenon observed in the gamma-ray radiation-induced hydrophobic effects on an Invar surface: When the Invar alloy is subjected to different doses of gamma-ray irradiation, the contact angle increases with the radiation dose. Invar samples with exposed to a higher dose appear more hydrophobic, but this tendency disappears following post-irradiation etching. The contact angles of the irradiated and etched Invar samples can be restored back to a stable value with small deviation after 30 min of annealing at 150°C. X-ray diffraction (XRD) analysis found no crystalline structural changes. High resolution field emission scanning microscope (FE-SEM) analyses showed that irradiation might induce crack-like surfaces which could be removed at higher radiation dose in the following acid etchings. It is believed that the chemical bonds of Invar oxide on the surface were broken by the gamma-ray irradiation, thus raising the likelihood of binding with free ions in the air and resulting in the exclusion of the hydrophilic OH bonds, leaving a hydrophobic post-irradiation Invar surface.


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