Rongxin Su

Ethanol production from high dry matter corncob using fed-batch simultaneous saccharification and fermentation after combined pretreatment.

To obtain high concentration of ethanol from cellulose, corncob was pretreated with acid and alkali to remove non-cellulose components, and then subjected to simultaneous saccharification and fermentation (SSF). An ethanol concentration as high as 69.2 g/L was achieved with 19% dry matter (DM) using batch SSF, resulting in an 81.2% overall ethanol yield. A fed-batch process using a high solid concentration was also investigated. Fresh substrate was pretreated with dilute sulfuric acid-sodium hydroxide, and then added at different amounts during the first 24 h, to yield a final dry matter content of 25% (w/v). SSF conditions with cellulose loading of 22.8 FPU/g glucan, dry yeast (Saccharomyces cerevisiae) loading of 5 g/L and substrate supplementation every 4h yielded the highest ethanol concentration of 84.7 g/L after 96 h. This corresponded to a 79% overall ethanol yield.

Bioconversion of Lignocellulose into Bioethanol: Process Intensification and Mechanism Research

Biofuels produced from lignocellulosic biomass can significantly reduce the energy dependency on fossil fuels and the resulting effects on environment. In this respect, cellulosic ethanol as an alternative fuel has the potential to become a viable energy source in the near future. Over the past few decades, tremendous effort has been undertaken to make cellulosic ethanol cost competitive with conventional fossil fuels. The pretreatment step is always necessary to deconstruct the recalcitrant structures and to make cellulose more accessible to enzymes. A large number of pretreatment technologies involving physical, chemical, biological, and combined approaches have been developed and tested at the pilot scale. Furthermore, various strategies and methods, including multi-enzyme complex, non-catalytic additives, enzyme recycling, high solids operation, design of novel bioreactors, and strain improvement have also been implemented to improve the efficiency of subsequent enzymatic hydrolysis and fermentation. These technologies provide significant opportunities for lower total cost, thus making large-scale production of cellulosic ethanol possible. Meanwhile, many researchers have focused on the key factors that limit cellulose hydrolysis, and analyzing the reaction mechanisms of cellulase. This review describes the most recent advances on process intensification and mechanism research of pretreatment, enzymatic hydrolysis, and fermentation during the production of cellulosic ethanol.

Facile in situ synthesis of silver nanoparticles on procyanidin-grafted eggshell membrane and their catalytic properties.

Facile, efficient, and robust immobilization of metal nanostructures on porous bioscaffolds is an interesting topic in materials chemistry and heterogeneous catalysis. This study reports a facile in situ method for the synthesis and immobilization of small silver nanoparticles (AgNPs) at room temperature on natural eggshell membrane (ESM), which presents interwoven fibrous structure and can be used as a unique protein-based biotemplate. Procyanidin (Pro), a typical plant polyphenol extracted from grape seeds and skins, was first grafted onto ESM fibers to serve as both reductant and stabilizer during the synthesis process. As a result, the AgNPs were facilely synthesized and robustly immobilized on the ESM fibers without additional chemical reductant or physical treatments. The morphology and microstructure of the as-prepared AgNPs@Pro-ESM composites were characterized by combined microscopy and spectroscopy technologies. The results indicate that small AgNPs with mean diameter of 2.46 nm were successfully prepared on the Pro-ESM biotemplate. The composites exhibited good catalytic activity toward the reduction of 4-nitrophenol (4-NP). More importantly, these composite catalysts can be easily recovered and reused for more than eight cycles because of their high stability.

Self-assembling peptide–polysaccharide hybrid hydrogel as a potential carrier for drug delivery

Here we report a novel peptide–polysaccharide hybrid hydrogel as a potential carrier for sustained delivery of hydrophobic drugs. The hybrid hydrogel composed of Fmoc-diphenylalanine (Fmoc-FF) peptide and konjac glucomannan (KGM) was prepared through molecular self-assembly of Fmoc-FF in the KGM solution. The physicchemical properties of the Fmoc-FF–KGM hybrid hydrogel were further evaluated. This hybrid hydrogel exhibited a highly hydrated, rigid and nanofibrous gel network in which self-assembled peptide nanofibers were interwoven with the KGM chains. The results of a stability test and rheology study showed that the hybrid hydrogel has much higher stability and mechanical strength compared to Fmoc-FF hydrogel alone. Both CD and FTIR analysis indicated an anti-parallel β-sheet arrangement of Fmoc-FF peptide in self-assembled nanofibers, regardless the presence of KGM. Moreover, docetaxel was chosen as a model of hydrophobic drugs and incorporated into hydrogels to study the in vitro release behavior. The sustained and controlled drug release from this hybrid hydrogel was achieved by varying the KGM concentration, molecular weight, aging time or β-mannanase concentration. Our results not only provide a new strategy for fabricating Fmoc-FF–KGM hybrid hydrogel as a sustained-release drug carrier but also open an avenue for the design of new self-assembling peptide–polysaccharide hybrid hydrogels.

Synthesis of well-dispersed Ag nanoparticles on eggshell membrane for catalytic reduction of 4-nitrophenol

A novel functional bio-nanocomposite was prepared by deposition of Ag nanoparticles onto the surface of natural eggshell membrane fibers. Practically, the functional groups exposed on the fiber surface can provide locations to anchor Ag ions when immersed into metal precursor solution. The synthesized small-sized Ag nanoparticles with uniform distribution is well decorated on the surface of interwoven fibers of eggshell membrane. The effectiveness of the as-prepared AgNPs/ESM composites as a solid phase heterogeneous catalyst has been evaluated, for the first time, on the well-known 4-nitrophenol reduction to 4-aminophenol in the presence of excess borohydride. Moreover, the kinetics of the reduction reaction was investigated at different temperatures to determine the activation energy. This work provides an important example in the introduction of natural membranes for the fabrication of functional hybrid nanocomposites which could be very useful in varying fields.

Rational Design of Chiral Nanostructures from Self-Assembly of a Ferrocene-Modified Dipeptide

We report a new paradigm for the rational design of chiral nanostructures that is based on the hierarchical self-assembly of a ferrocene (Fc)-modified dipeptide, ferrocene-L-Phe-L-Phe-OH (Fc-FF). Compared to other chiral self-assembling systems, Fc-FF is unique because of its smaller size, biocompatibility, multiple functions (a redox center), and environmental responsiveness. X-ray and spectroscopic analyses showed that the incorporation of counterions during the hierarchical self-assembly of Fc-FF changed the conformations of the secondary structures from flat β sheets into twisted β sheets. This approach enables chiral self-assembly and the formation of well-defined chiral nanostructures composed of helical twisted β sheets. We identified two elementary forms for the helical twist of the β sheets, which allowed us to create a rich variety of rigid chiral nanostructures over a wide range of scales. Furthermore, through subtle modulations in the counterions, temperature, and solvent, we are able to precisely control the helical pitch, diameter, and handedness of the self-assembled chiral nanostructures. This unprecedented level of control not only offers insights into how rationally designed chiral nanostructures can be formed from simple molecular building blocks but also is of significant practical value for the use in chiroptics, templates, chiral sensing, and separations.

Porous-CLEAs of papain: application to enzymatic hydrolysis of macromolecules.

Porous cross-linked enzyme aggregates (p-CLEAs) were prepared by adding starch as a pore-making agent, which facilitates CLEAs in cases where the substrates of enzyme are macromolecules. This novel strategy for preparation of p-CLEAs involves co-precipitation, cross-linking and removal of starch by α-amylase. The resulting papain p-CLEAs were characterized by scanning electron microscope (SEM) images, showing a porous structure. The 95.9% and 90.4% increased catalytic efficiencies of p-CLEAs than conventional CLEAs on bovine serum albumin (BSA) and ovalbumin verified the feasibility of this protocol.

Solvent and surface controlled self-assembly of diphenylalanine peptide: from microtubes to nanofibers

A new approach based on solvent and surface effects was developed for controlling the self-assembly of diphenylalanine peptide into microtubes and nanofibers. The HBD/HBA ability and surface tension may be major determinants in the formation of these peptide assemblies. Our results will lead to a better understanding of the molecular mechanisms involved in diphenylalanine self-assembly process.

Grafting hyaluronic acid onto gold surface to achieve low protein fouling in surface plasmon resonance biosensors.

Antifouling surfaces capable of reducing nonspecific protein adsorption from natural complex media are highly desirable in surface plasmon resonance (SPR) biosensors. A new protein-resistant surface made through the chemical grafting of easily available hyaluronic acid (HA) onto gold (Au) substrate demonstrates excellent antifouling performance against protein adsorption. AFM images showed the uniform HA layer with a thickness of ∼10.5 nm on the Au surface. The water contact angles of Au surfaces decreased from 103° to 12° with the covalent attachment of a carboxylated HA matrix, indicating its high hydrophilicity mainly resulted from carboxyl and amide groups in the HA chains. Using SPR spectroscopy to investigate nonspecific adsorption from single protein solutions (bovine serum albumin (BSA), lysozyme) and complex media (soybean milk, cow milk, orange juice) to an HA matrix, it was found that ultralow or low protein adsorptions of 0.6-16.1 ng/cm(2) (e.g., soybean milk: 0.6 ng/cm(2)) were achieved on HA-Au surfaces. Moreover, anti-BSA was chosen as a model recognition molecule to characterize the immobilization capacity and the antifouling performance of anti-BSA/HA surfaces. The results showed that anti-BSA/HA sensor surfaces have a high anti-BSA loading of 780 ng/cm(2), together with achieving the ultralow (<3 ng/cm(2) for lysozyme and soybean milk) or low (<17 ng/cm(2) for cow milk and 10% blood serum) protein adsorptions. Additionally, the sensor chips also exhibited a high sensitivity to BSA over a wide range of concentrations from 15 to 700 nM. Our results demonstrate a promising antifouling surface using extremely hydrophilic HA as matrix to resist nonspecific adsorption from complex media in SPR biosensors.

Synthesis of silver nanoparticles within cross-linked lysozyme crystals as recyclable catalysts for 4-nitrophenol reduction

For the first time, we demonstrated the fabrication of silver nanoparticles (NPs) in cross-linked protein crystal hybrid material with catalytic properties using a facile chemical reduction method. The macroscopic porous lysozyme crystals can be used as excellent templates for the incorporation of Ag nanoparticles. The resulting AgNP-in-lysozyme crystal composites exhibited a good catalytic activity toward nitrophenol reduction. Notably, these catalysts could be easily recovered and reused for at least five successive cycles with almost constant activity and conversion efficiency.