Mutagenesis of Novel <i>Clostridial fusants</i> for Enhanced Green Biobutanol Production from Agriculture Waste

In an earlier investigation, novel Clostridial fusants were introduced and demonstrated an ability to produce biobutanol at the relatively high temperature of 45 °C. The objective of the present study is to further improve the fused strains through examining the impact of mutation agents on their stability, tolerance to biobutanol toxicity and biofuel production capability. The results for the mutated strains showed enhanced resistance to biobutanol by the fused strains and better biobutanol generation by cells. Furthermore, the results showed high biobutanol production (14.7–15 g/L), with a total Acetone, Biobutanol and Ethanol (ABE) yield of 0.6 g/g. Moreover, mutated strains showed tolerance to biobutanol toxicity up to 15 g/L, which is equivalent to a ~15% increase over literature values. The oxygen tolerance study showed improved performance by the mutated anaerobic fusant. In general, the mutation of fused clostridium strains using UV and EMS leads to the identification of stronger robust strains that show higher tolerance to oxygen and biobutanol toxicity and achieved higher yield

Novel thermostable clostridial strains through protoplast fusion for enhanced biobutanol production at higher temperature—preliminary study

The objective of this study is to improve the thermal stability of clostridium strains for enhanced biobutanol production. Thermostable clostridia species were developed through protoplast fusion between mesophilic clostridial species (i.e., Clostridium beijerinckii and Clostridium acetobutylicum) and thermophilic clostridial species (i.e., Clostridium thermocellum). Production of biobutanol was examined in the present preliminary study using the clostridium strains and their protoplast fusants using sugar mixture with composition identical to that of wheat straw acid hydrolysate. Maximum biobutanol production of 9.4 g/L was achieved by a fused strain at 45 °C with total sugar consumption of 66% compared to that at 35 °C (i.e., 8.4 g/L production and 64% total sugar consumption). Glucose and xylose uptake rates were generally higher compared to all other individual sugars in the feedstock. In general, average cell concentrations were in close proximity for all parenting and fused strains at 35 °C; i.e., in the range of 5.12 × 107 to 5.49 × 107 cells/mL. Average cell concentration of fusants between the mesophilic clostridial species and the thermophilic clostridial species slightly increased to ~ 5.62 × 107 cells/mL at a higher temperature of 45 °C. These results, in addition to the ones obtained for the butanol production, demonstrate enhanced thermal stability of both fusants at a higher temperature (45 °C)

Novel thermostable clostridial strains through protoplast fusion for enhanced biobutanol production at higher temperature—preliminary study

The objective of this study is to improve the thermal stability of clostridium strains for enhanced biobutanol production. Thermostable clostridia species were developed through protoplast fusion between mesophilic clostridial species (i.e., Clostridium beijerinckii and Clostridium acetobutylicum) and thermophilic clostridial species (i.e., Clostridium thermocellum). Production of biobutanol was examined in the present preliminary study using the clostridium strains and their protoplast fusants using sugar mixture with composition identical to that of wheat straw acid hydrolysate. Maximum biobutanol production of 9.4 g/L was achieved by a fused strain at 45 °C with total sugar consumption of 66% compared to that at 35 °C (i.e., 8.4 g/L production and 64% total sugar consumption). Glucose and xylose uptake rates were generally higher compared to all other individual sugars in the feedstock. In general, average cell concentrations were in close proximity for all parenting and fused strains at 35 °C; i.e., in the range of 5.12 × 107 to 5.49 × 107 cells/mL. Average cell concentration of fusants between the mesophilic clostridial species and the thermophilic clostridial species slightly increased to ~ 5.62 × 107 cells/mL at a higher temperature of 45 °C. These results, in addition to the ones obtained for the butanol production, demonstrate enhanced thermal stability of both fusants at a higher temperature (45 °C).</p

Novel Thymine-functionalized Polystyrenes for Applications in Biotechnology Ii. Adsorption of Model Proteins

This paper investigates the adsorption of bovine serum albumin (BSA) and bovine hemoglobin (BHb) model proteins onto novel thymine-functionalized polystyrene (PS−VBT) microspheres, in comparison with polystyrene (PS) microspheres. Maximum adsorption was obtained for both proteins near their corresponding isoelectric points (pI at pH = 4.7 for BSA and 7.1 for BHb). FTIR and adsorption isotherm analysis demonstrated that, although both proteins were physisorbed onto PS through nonspecific hydrophobic interactions, adsorption onto the functionalized copolymers occurred by both physisorption and chemisorption via hydrogen bonding. FTIR analysis also indicated conformational changes in the secondary structure of BSA and BHb adsorbed onto PS, whereas little or no conformation change was seen in the case of adsorption onto PS−VBT. Atomic force microscopy (AFM), consistent with the isotherm results, also demonstrated monolayer adsorption for both proteins. AFM images of BSA adsorbed onto copolymers with 20 mol % surface VBT loading showed exclusively end-on orientation. Adsorption onto copolymers with lower functionality showed mixed end-on and side-on orientation modes of BSA, and only the side-on orientation was observed on PS. The AFM results agreed well with theoretically calculated and experimentally obtained adsorption capacities. AFM together with calculated and observed adsorption capacity data for BHb indicated that this protein might be highly compressed on the copolymer surface. Adsorption from a binary mixture of BSA and BHb onto PS−VBT showed good separation at pH=7.0; ∼ 90% of the adsorbed protein was BHb. The novel copolymers have potential applications in biotechnology

Polyisobutylene-based Biomaterials

This article highlights the biomaterial-related research of the Macromolecular Engineering Research Centre (MERC). The MERC group concentrated on polyisobutylene (PIB)-based biomaterials. In this article, first the unique properties of PIB are discussed, followed by a review of PIB-based potential biomaterials. MERC\u27s systematic research program aimed to develop novel PIB-based biomaterials is then highlighted, including surface modification and biocompatibility studies. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 3091–3109, 200

A Review on Anaerobic Co-Digestion with a Focus on the Microbial Populations and the Effect of Multi-Stage Digester Configuration

Recent studies have shown that anaerobic co-digestion (AnCoD) is superior to conventional anaerobic digestion (AD). The benefits of enhanced bioenergy production and solids reduction using co-substrates have attracted researchers to study the co-digestion technology and to better understand the effect of multi substrates on digester performance. This review will discuss the results of such studies with the main focus on: (1) generally the advantages of co-digestion over mono-digestion in terms of system stability, bioenergy, and solids reduction; (2) microbial consortia diversity and their synergistic impact on biogas improvement; (3) the effect of digester mode, i.e., multi-stage versus single stage digestion on AnCoD. It is essential to note that the studies reported improvement in the synergy and diverse microbial consortia when using co-digestion technologies, in addition to higher biomethane yield when using two-stage mode. A good example would be the co-digestion of biodiesel waste and glycerin with municipal waste sludge in a two-stage reactor resulting in 100% increase of biogas and 120% increase in the methane content of the produced biogas with microbial population dominated by Methanosaeta and Methanomicrobium

Viscoelastic behavior and mechanical properties of polypropylene/nano-calcium carbonate nanocomposites modified by a coupling agent

Polymer blends have the potential to be developed into new resins for specific applications with balanced performance properties and economic advantages. In this paper, polypropylene (PP) and linear low-density polyethylene (LLDPE) blends were investigated at specific composition of PP/LLDPE (60/40) blends (PL40) using a Twin Screw Extruder (TSE). The nano-calcium carbonate (CaCO3) content was varied (between 0-40 wt %), and the composites were investigated using slit die rheometers. Fourier transform infrared (FTIR) spectroscopy and X-ray diffraction (XRD) techniques, revealed the existence of favorable interaction between the surface of CaCO3 nanoparticles and PL40 matrices after surface modification of aminopropyltriethoxy silane (AMPTES) coupling agent. Rheological properties reveal that both the apparent viscosity and the pseudo-plasticity of the PL40 nanocomposites increases with increasing nano-CaCO3 contents and decreases slightly by treated nano-CaCO3 with 2% AMPTES. Dynamic mechanical analysis (DMA) demonstrated that the storage modulus (G′) and glass transition temperature (Tg) are enhanced upon treated nano-CaCO3 with a coupling agent. The results from the mechanical properties exhibited that the impact strength was optimum at 20% nano-CaCO3 content, but tensile strength slightly decreased for untreated PL40 nanocomposites. However, treatment with amino coupling agent improved tensile strength. This attribute to the enhancement of dispersion of the nano-CaCO3 particles in PL40 matrix, leading to improved interfacial adhesion. Treatment of nano-CaCO3 significantly improved the Young’s modulus and flexural modulus compared to the untreated PL40 composites. The crystallization behavior of the composites supported the strong interfaces formed on addition of the amino coupling agent. Furthermore, scanning electron microscopic (SEM) showed evidence of improvement in the dispersion of treated CaCO3 in the PL-40 matrix

Biomass processing into ethanol: pretreatment, enzymatic hydrolysis, fermentation, rheology, and mixing

Alternate energy resources need to be developed to amend for depleting fossil fuel reserves. Lignocellulosic biomass is a globally available renewable feedstock that contains a rich sugar platform that can be converted into bioethanol through appropriate processing. The key steps of the process, pretreatment, enzymatic hydrolysis, and fermentation, have undergone considerable amount of research and development over the past decades nearing the process to commercialization. In order for the commercialization to be successful, the process needs to be operated at high dry matter content of biomass, especially in the enzymatic hydrolysis stage that influences ethanol concentration in the final fermentation broth. Biomass becomes a thick paste with challenging rheology for mixing to be effective. As the biomass consistency increases, yield stress increases which limits efficiency of mixing with conventional stirred tanks. The purpose of this review is to provide features and perspectives on processing of biomass into ethanol. Emphasis is placed on rheology and mixing of biomass in the enzymatic hydrolysis step as one of the forefront issues in the field.</p