Effect of Rhodococcus sp. pretreatment on cellulose hydrolysis of corn stalk.

Pretreatment can improve the hydrolysis efficiency of cellulose, in which biological pretreatment plays an important role. In the present study, we uncovered that Rhodococcus has the ability of lignin degradation, which can decompose lignin and serve as a carbon source to meet the needs of its own growth. We used Rhodococcus to pretreat the corn stalks and evaluate the effect on cellulose hydrolysis. The concentration of reducing sugar produced by the hydrolysis of corn stalk after pretreatment of Rhodococcus is 2.95 g/L. SEM imaging showed that Rhodococcus pretreatment resulted the surface of corn stalk to be no longer complete, some lamellar structures fall off, and leave obvious traces, and obvious delamination was found at the edge of the fault. AFM imaging showed that the pretreatment changed the lignin structure of the corn stalk material surface, resulting in a higher surface roughness of 9.37. These results indicated that Rhodococcus pretreatment can improve the saccharification efficiency of cellulose by removing lignin and increasing the surface roughness of the material.

Enhanced upconversion luminescence through core/shell structures and its application for detecting organic dyes in opaque fishes.

Here, we report the enhanced upconversion luminescence of NaLuF4:18%Yb(3+),2%Er(3+) through core/shell structures. Among NaYF4, NaGdF4, and NaLuF4 shells, the first one presents the highest efficiency. These upconversion fluorescent nanoprobes with an oleic acid/PEG hybrid ligand can efficiently capture Rhodamine B (RB) and sodium fluorescein (SF) in opaque fishes to present their residues in vivo through luminescence resonant energy transfer (LRET) processes. It can be confirmed based on LRET technology that no RB is absorbed by opaque fishes after incubating in the aqueous solution of 1 µg ml(-1) RB for one day, while SF residue can be obviously detected after incubating in the aqueous solution of 1 µg ml(-1) SF for one day. The merit of this LRET technology with the upconversion nanoparticle (UCNP) donor is ascribed to the deep penetration depth of the infrared pumping laser and high signal to noise ratio.

Surface modification of commercial intraocular lens by zwitterionic and antibiotic-loaded coating for preventing postoperative endophthalmitis.

After cataract surgery, to prevent possible postoperative endophthalmitis (POE) caused by attached pathogenic bacteria onto the surface of implanted intraocular lens (IOL), various antibiotic-loaded IOLs have been proposed and widely studied to inhibit bacterial infection. However, most of these developed antibiotic-loaded IOLs still suffer from shortcomings such as insufficient drug loading, short release time, poor biocompatibility, and risk of secondary infection. Herein, we propose a zwitterionic and high-drug loading coating for surface modification of commercial hydrophobic IOL with both antifouling and antibacterial properties to effectively prevent POE. In this strategy, zwitterionic poly(carboxylbetaine-co-dopamine methacrylamide) copolymers (pCBDA) and dopamine (DA) were first robustly co-deposited onto IOL surface via facile mussel-inspired chemistry, resulting in a hydrophilic coating (defined as PCB) without sacrificing the high light transmittance of the native IOL. Subsequently, amikacin (AMK), an amine-rich antibiotic was reversibly conjugated onto the coating through the acid-sensitive Schiff base bonds formed by the reaction between amino and catechol groups, with high-drug payload over ∼35.5 µg per IOL and 30 days of sustained drug release under weak acid environment. Benefiting from the antifouling property of zwitterionic pCBDA copolymers, the intraocularly implanted PCB/AMK-coated IOL could effectively resist the adhesion and proliferation of residual LECs to inhibit the development of posterior capsule opacification (PCO) without affecting the normal ocular tissues, demonstrating excellent in vivo biocompatibility. Moreover, the synergy of zwitterionic pCBDA and conjugated AMK with acidic-dependent release behavior endowed this PCB/AMK-coated IOL strong antibacterial activity against both in vitro biofilm formation and in vivo postoperative Staphylococcus aureus infection, suggesting its promising application in preventing POE.

Efficient removal of nano- and micro- sized plastics using a starch-based coagulant in conjunction with polysilicic acid.

Microplastic (MP) pollution has increasingly become an enormous global challenge due to the ubiquity and uncertain environmental performance, especially for nano- and micro- sized MPs. In this work, the performance and mechanisms in coagulation of 100 nm-5.0 µm sized polystyrene particles using an etherified starch-based coagulant (St-CTA) assisted by polysilicic acid (PSA) were systematically studied on the basis of the changes in MPs removal rates under various pH levels and in the presence of different coexisting inorganic and organic substances, zeta potentials of supernatants, and floc properties. St-CTA in conjunction with PSA had a high performance in coagulation of nano- and micro- sized MPs from water with a lower optimal dose and larger and compacter flocs. Besides, the MPs removal rate can be improved in acidic and coexisting salt conditions. The efficient performance in removal of MPs by this enhanced coagulation was owing to the synergic effect, that is, the effective aggregation of MPs through the charge neutralization of St-CTA followed by the efficient netting-bridging effect of PSA. The effectiveness of this enhanced coagulation was further confirmed by removal of two other typical nano-sized MPs, such as poly(methyl methacrylate) and poly(vinyl chloride), from different water sources including tap water, river water, and sludge supernatant from a sewage treatment plant. This work provided a novel enhanced coagulation technique that can effectively remove nano- and micro- sized MPs from water.

Comparison of two starch-based flocculants with polyacrylamide for the simultaneous removal of phosphorus and turbidity from simulated and actual wastewater samples in combination with FeCl3.

Two laboratory-made cationic starch-based flocculants (St-CTA and St-AD) with different chain architectures were used to simultaneously remove phosphorus and turbidity from two simulated wastewaters and one actual wastewater with laboratory and pilot scales, respectively, in conjunction with FeCl3. A commercial polyacrylamide (PAM) has been also tried and compared with aforementioned starch-based flocculants. The removal extents of phosphorus and turbidity increased, the required dosages of FeCl3 decreased, and floc properties improved after dosing each polymeric flocculant after FeCl3 in all tested wastewaters due to their synergistic effects. However, the three flocculants exhibited different improvement efficiencies on the treated wastewaters containing different forms of phosphorus and showed various synergistic mechanisms owing to their distinct structural features. In inorganic-phosphorus-simulated wastewater, the linear nonionic PAM with a high molecular weight had a more notable contribution than the two starch-based flocculants due to its efficient bridging flocculation effect. Given the branched-chain structure and high positive charge density of St-AD, it had a higher efficiency in treating real wastewater and organic-phosphorus-simulated wastewater than PAM and linear cationic St-CTA. These results may serve as references for the design and selection of a suitable flocculant in treating target wastewaters.

Titanium Alloy Gamma Nail versus Biodegradable Magnesium Alloy Bionic Gamma Nail for Treating Intertrochanteric Fractures: A Finite Element Analysis.

OBJECTIVE: To using finite element analysis to investigate the effects of the traditional titanium alloy Gamma nail and a biodegradable magnesium alloy bionic Gamma nail for treating intertrochanteric fractures. METHODS: Computed tomography images of an adult male volunteer of appropriate age and in good physical condition were used to establish a three-dimensional model of the proximal femur. Then, a model of a type 31A1 intertrochanteric fracture of the proximal femur was established, and the traditional titanium alloy Gamma nails and biodegradable magnesium alloy bionic Gamma nails were used for fixation, respectively. The von Mises stress, the maximum principal stress, and the minimum principal stress were calculated to evaluate the effect of bone ingrowth on stress distribution of the proximal femur after fixation. RESULTS: In the intact model, the maximum stress was 5.8 MPa, the minimum stress was -11.7 MPa, and the von Mises stress was 11.4 MPa. The maximum principal stress distribution of the cancellous bone in the intact model appears in a position consistent with the growth direction of the principal and secondary tensile zones. After traditional Gamma nail healing, the maximum stress was 32 MPa, the minimum stress was -23.5 MPa, and the von Mises stress was 31.3 MPa. The stress concentration was quite obvious compared with the intact model. It was assumed that the nail would biodegrade completely within 12 months postoperatively. The maximum stress was 18.7 MPa, the minimum stress was -12.6 MPa, and the von Mises stress was 14.0 MPa. For the minimum principal stress, the region of minimum stress value less than -10 MPa was significantly improved compared with the traditional titanium alloy Gamma nail models. Meanwhile, the stress distribution of the bionic Gamma nail model in the proximal femur was closer to that of the intact bone, which significantly reduced the stress concentration of the implant. CONCLUSION: The biodegradable magnesium alloy bionic Gamma nail implant can improve the stress distribution of fractured bone close to that of intact bone while reducing the risk of postoperative complications associated with traditional internal fixation techniques, and it has promising clinical value in the future.

Evaluation of the structural factors for the flocculation performance of a co-graft cationic starch-based flocculant.

Three series of co-graft cationic starch (St)-based flocculants with distinct structural characteristics, namely, charge density (CD), graft-chain length (L), and graft-chain distribution (N), were successfully synthesized through graft copolymerization of [(2-methacryloyloxyethyl) trimethyl ammonium chloride] and acrylamide. These St-based flocculants with different molecular structures were used to flocculate various kaolin suspensions with different initial turbidities and a sodium humate (NaHA) aqueous solution. The experimental results indicated that CD contributed to flocculation evidently, whereas average L and its N were insignificant in experimentally measured ranges. On the basis of phenomenological theory, a second-order polynomial equation was used to further quantitatively analyze the effects of the three structural factors on the flocculation performance of these St-based flocculants, which were fully consistent with the experimental results. Besides, the optimal dose and its corresponding removal rate could be predicted exactly, and the flocculation mechanisms were discussed in detail according to the established models. With the combination of floc properties and zeta potentials, the flocculation mechanisms of these St-based flocculants for flocculation of kaolin suspensions and NaHA aqueous solution were mainly ascribed to charge patching and simple charge neutralization, respectively. These results improve the understanding of the structure-activity relationship of these graft St-based flocculants, which is of significant guidance for the utilization and design of novel flocculants.

Effect of Particle Size Ratios on the Physical and Chemical Properties of Surgical-Grade Calcium Sulfate Hemihydrate.

OBJECTIVES: To analyze the optimum particle size or formula ratio of surgical-grade calcium sulfate (CS) for appropriate compressive strength, setting time, and vitro degradation rate. METHODS: Three types of calcium sulfate hemihydrate (CSH) particles with diameters of 0-37.5 µm, 37.5-75 µm, and >75 µm were screened. Based on formulation ratio of different particles, this topic is divided into 10 groups by the unconstrained third-order simplex lattice mixing design scheme in formula design experiment. The optimum formulation ratio of particle diameter for compressive strength, solidification time, and degradation rate in vitro was analyzed. RESULTS: When the percentage of the particle diameter of CS with 0-37.5 µm, 37.5-75 µm and >75 µm are 55.0%, 17.4%, and 27.6% respectively, the compressive strength of the test sample is the highest, which is 14.16 MPa. When the percentage of the particle diameter of CS with 0-37.5 µm, 37.5-75 µm, and >75 µm are 0.00%, 0.00%, and 100.00% respectively, the initial setting time of the sample is the longest, which is 410.0 s. When the percentage of the particle diameter of CS with 0-37.5 µm, 37.5-75 µm, and >75 µm are 0.00%, 0.00%, and 100.00% respectively, the final setting time of the sample is the largest, and the final setting time of the sample is 460.00 s. When the percentage of the particle diameter of CS with 0-37.5 µm, 37.5-75 µm, and >75 µm are 0.00%, 0.00%, and 100.00% respectively, the degradation rate of the sample in vitro is the slowest, which is 18.8%. CONCLUSION: The morphological structure of surgical-grade CS can affect compressive strength, setting time, and in vitro degradation rate. Surgical CS should be prepared based on different uses.

Dissecting the effect of polyethylene glycol on the enzymatic hydrolysis of diverse lignocellulose.

Natural lignocellulose is used as raw material to produce chemicals through biological transformation. The accessibility of cellulase to substrate was also one of the limiting factors of industrial production. Polyethylene glycol (PEG) can be used as additive in enzymatic hydrolysis of lignocellulose. In this study, enzymatic activity on simultaneous or non-simultaneous addition of PEG 4000 was investigated, and the partly delignified rice straw, the rice straw and filter paper were used as substrates, respectively. Enzyme activity was characterized by reducing sugar concentration in supernatant which was quantified through 3,5-dinitrosalicylic acid (DNS) method. Addition of PEG has been proven to facilitate enzymatic hydrolysis of lignocellulosic materials. Furthermore, PEG had the positive effect on hydrolytic enzyme activity of pure cellulose materials without lignin. Changes in lignocellulose materials have been observed by inverted microscope and Scanning electron microscope (SEM), and no chemical changes were shown by Fourier transform infrared spectroscopy (FTIR). The promotion of PEG on enzymatic hydrolysis of pure cellulose materials may be due to its loose physical structure and similar phenomenon in natural lignin materials. PEG loosens the physical structure of lignocellulose, thus facilitating enzymatic hydrolysis. This may be a new idea to optimize the lignocellulosic enzymatic hydrolysis process.

Co-expression of cellulase and xylanase genes in Sacchromyces cerevisiae toward enhanced bioethanol production from corn stover.

Lignocellulose is considered as a good resource for producing renewable energy. Previous in vitro studies have shown the synergistic action between cellulase and xylanase during lignocellulose biohydrolysis. In order to achieve the same effect in S. cerevisiae to enhance the practical biotransformation, two recombinant Saccharomyces cerevisiae strains (INVSc1-CBH-CA and INVSc1-CBH-TS) with co-expressed cellulase and xylanase were constructed. The cellulase and xylanase activities in INVSc1-CBH-CA and INVSc1-CBH-TS were 716.43 U/mL and 205.13 U/mL, 931.27 U/mL and 413.70 U/mL, respectively. The recombinant S. cerevisiae can use the partly delignified corn stover (PDCS) more efficiently and more ethanol producted than S. cerevisiae only expressing cellulase. Fermentation with INVSc1-CBH-CA and INVSc1-CBH-TS using PDCS ethanol yields increased by 1.7 and 2.1 folds higher than INVSc1-CBH, 2.8 and 3.4 folds higher than the wild type S. cerevisiae. The strategy of co-expression cellulase and xylanase in saccharomyces cerevisiae is effective and can be a foundation to research the mechanism of synergy effect of cellulose and xylanase.

"H"-shape second order NLO polymers: synthesis and characterization.

In this work, two "H"-shape and one "AB"-type second order nonlinear optical (NLO) polymers were prepared for the first time. The linkage positions of chromophores in the "H"-shape polymers were shoulder-to-shoulder, in which the chromophore moieties were part of the polymeric backbone. The subtle structure could be easily modified by the introduction of different isolation groups, to adjust the property of the resultant polymers. All the polymers exhibited good film-forming ability and thermal stability. The second harmonic generation (SHG) experiments demonstrated that the two "H"-shape polymers (P1 and P2) exhibited large SHG coefficients of d(33) values (up to 90 pm V(-1)), and P2 even demonstrated relatively good long-term temporal stability.