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The pulp and biorefining industries produce their waste as lignin, which is one of the most abundant renewable resources. So far, lignin has been remained severely underutilized and generally burnt in a boiler as a low-value fuel. To demonstrate lignin's potential as a value-added product, we will review market opportunities for lignin related applications by utilizing the thermo-chemical/biological depolymerization strategies (with or without catalysts) and their comparative evaluation. The application of lignin and its derived aromatics in various sectors such as cement industry, bitumen modifier, energy materials, agriculture, nanocomposite, biomedical, H

Rice straw has a great potential for ethanol production due to its richness in polysaccharides and abundant availability, however, for efficient utilization of these polysaccharides, size reduction is a prerequisite step. Therefore, biomass particle size plays a vital role for cellulosic ethanol commercialization. In this study, the effects of rice straw particle size on dilute acid pretreatment efficiency and enzymatic hydrolysis are investigated. Different sizes; 5, 10 and 20 mm were subjected to dilute acid pretreatment in a continuous pilot scale system with a horizontal screw feeder reactor followed by enzymatic hydrolysis at varying solids (10 and 15%) and enzyme dosages (5 and 10 FPU/g of pretreated residue). The glucan hydrolysis for 5, 10 and 20 mm are 65.6, 80.0 and 60.0% using 5 FPU and 79.5, 93.4 and 72.8% using 10 FPU/g pretreated residue respectively at 10% loading, whereas, at 15% it is significantly lower in respective experiment. Overall sugar recovery with 10 mm is 63.8 and 72.9% with 5 and 10 FPU respectively. RS with 10 mm biomass particle size at both solid loadings and enzyme dosages resulted in much higher enzymatic hydrolysis than others and in turn the overall sugar recovery and this was found to be due to the variation in the degradation products and pseudolignin contents in the pretreated biomass. The insight into the structural intricacies of biomass after pretreatment are studied using FT-IR and SEM revealing significant changes in biomass properties responsible for improved sugar recovery.

Conversion of lignocellulosic biomass to fuels and chemicals has attracted immense research and development around the world. Lowering recalcitrance of biomass in a cost-effective manner is a challenge to commercialize biomass-based technologies. Deep eutectic solvents (DESs) are new 'green' solvents that have a high potential for biomass processing because of their low cost, low toxicity, biodegradability, easy recycling and reuse. This article discusses the properties of DESs and recent advances in their application for lignocellulosic biomass processing. The effectiveness of DESs in hydrolyzing lignin-carbohydrate complexes, removing lignin/hemicellulose from biomass as well as their effect on biomass deconstruction, crystallinity and enzymatic digestibility have been discussed. Moreover, this review presents recent findings on the compatibility of natural DESs with enzymes and microorganisms.

Bioethanol from lignocellulosic biomass (LCB) is considered as an alternative solution to replace the fossil-based liquid fuels and thus causes the reduction in the environmental pollution in a sustainable manner. LCB is predominantly composed of cellulose, hemicellulose, lignin, ash, and extractives, which are interconnected with each other intricately leading to a rigid and recalcitrant structure. In its native form, enzymes could not access the carbohydrates and pretreatment is the key to disintegrate the highly ordered LCB structure and expose the cellulose and hemicellulose for enzymatic hydrolysis and release fermentable sugars. However, pretreatment is the high CAPEX (capital expenditure) and energy intensive step and it may represent up to 20%–30% of the ethanol costs. Thus, cost-effective and energy efficient pretreatment is the key to harness the potential of this largely untapped natural bioresource. Among various pretreatment strategies only a few have been validated at commercial scale (such as dilute acid, steam explosion, and hydrothermal) while most of them have only been evaluated at lab, pilot, or demonstration scale only (e.g., ammonia, alkali, biological, ionic liquids) majorly due to the poor economics and process complexity challenges. This study provides a detailed insight of the mechanism of action of different pretreatments, its impact on structural and functional properties of LCB with a focus on enzymatic hydrolysis yields. The analytical tools and techniques used to evaluate the substrate properties affected by the pretreatment and its correlation with enzymatic hydrolysis is discussed. Finally, the current status of pretreatment and enzymatic hydrolysis of different biomass at varied temperatures and solid loadings is illustrated to understand their impacts and implications.

Lignin is produced as a byproduct in cellulosic biorefinery as well in pulp and paper industries and has the potential for the synthesis of a variety of phenolics chemicals, biodegradable polymers, and high value-added chemicals surrogate to conventional petro-based fuels. Therefore, in this critical review, we emphasize the possible scenario for lignin isolation, transformation into value addition chemicals/materials for the economic viability of current biorefineries. Additionally, this review covers the chemical structure of lignocellulosic biomass/lignin, worldwide availability of lignin and describe various thermochemical (homogeneous/heterogeneous base/acid-catalyzed depolymerization, oxidative, hydrogenolysis etc.) and biotechnological developments for the production of bio-based low molecular weight phenolics, i.e. polyhydroxyalkanoates, vanillin, adipic acid, lipids etc. Besides, some functional chemicals applications, lignin-formaldehyde ion exchange resin, electrochemical and production of few targeted chemicals are also elaborated. Finally, we examine the challenges, opportunities and prospects way forward related to lignin valorization.

Novel and sustainable pretreatment approaches are desired to improve the techno-commercial feasibility of biorefineries in the future. In this study, 10 renewable deep eutectic solvents (DESs) were evaluated for their pretreatment efficiency at facile conditions with sugar cane bagasse as substrate and compared with conventional pretreatment approaches (dilute alkali, dilute acid, and ionic liquid (IL)) for lignin removal, saccharification yield, cellulose accessibility, crystallinity, and physiochemical properties. Although, the highest delignification was obtained with dilute alkali (59.7%) and choline chloride:lactic acid or ChCl:LA (50.6%), the maximum enzymatic conversion of 98.0% and 90.4% was observed with IL (1-butyl-3-methylimidazolium acetate) and ChCl:LA, respectively. uclear magnetic resonance analysis of ChCl:LA-derived lignin showed selective removal of guaiacyl lignin without condensation structure formation observed. Interestingly, unlike IL, the lignin was substantially depolymerized afte...

b-glucosidases are very important in the improvement of cellulose degradation rates by diminishing the inhibition of end products. Although, cellulase cost has reduced significantly in last decade but still the high costs of biomass saccharification is one of the main challenges for the commercialization of ethanol from LC biomass. In this work, -glucosidase immobilization in calcium alginate was optimized using response surface methodology. 89% immobilization efficiency was achieved under optimum conditions (i.e., calcium alginate 4.19% (w/v), calcium chloride 0.14 M and -glucosidase 4.42% (v/v) or 57.46 U/mL of reaction mixture). pH and temperature optima of both free and immobilized -glucosidase was found to be 5 and 50 C, respectively. Enzyme kinetics of free and immobilized -glucosidase was done to evaluate Michaelis constant (Km) and Vmax values, using pnitrophenyl- -D-glucopyranoside (pNPG) as the substrate and glucose as inhibitor. Increase in Km value (0.995 mM) for immobilized -glucosidase as compared to the free -glucosidase (0.617 mM) was observed. A decrease in Vmax from (1191.74 mol min-1 for free -glucosidase) to (736.65 mol min-1 immobilized -glucosidase) was observed after immobilization. Glucose was found to inhibit -glucosidase by competitive mode of inhibition (Ki= 3.01 mM). Studies were carried out in a batch reactor using 2% cellobiose, 0.1 M sodium acetate buffer, 5 pH and 50 C. 84% cellobiose to glucose conversion was found in first cycle which was about 67% in fifth cycle. This study suggests that enzyme immobilization improved enzyme stability, substrate inhibition and permits enzyme reusability.

3D printing by fused deposition modeling (FDM) is an advanced additive manufacturing technology for making thermoplastic-based structures. Several studies have recently investigated 3D printing of polylactic acid (PLA) with biomass resources like cellulose, hemicellulose, lignin and whole biomass. Such biodegradable composites are better for the environment and can be used to replace non-biodegradable composites in a variety of applications. Therefore, a deep understanding of printing such biocomposites is needed for supporting such manufacturing. Recent developments focused on FDM printing of PLA filled with biomass resources have been critically reviewed to reveal the intricate aspects of manufacturing of such materials and characterization of the changes caused by biomass-based fillers. Properties of high molecular weight PLA, essentials of printing with PLA and conditions for filament extrusion and printing of biocomposites are discussed. Characterization results from mechanical testing, thermal analysis, viscoelastic properties, imaging and spectroscopy are reviewed for understanding the impact of filling biomass resources in PLA by printing. The latter sections discuss applications, upcycling & recycling and future opportunities for biorefineries.

The surplus availability of rice straw, its limited usage, and environmental pollution caused by its inefficient burning has fostered research for its valorization to biofuels. This review elucidates the current status of rice straw potential around the globe along with recent advances in revealing the critical factors responsible for its recalcitrance and chemical properties. The role and accumulation of high silica content in rice straw has been elucidated with its impact on enzymatic hydrolysis in a biorefinery environment. The correlation of different pre-treatment approaches in modifying the physiochemical properties of rice straw and improving the enzymatic accessibility has also been discussed. This study highlights new challenges, resolutions, and opportunities for rice straw based biorefineries. © 2017 Society of Chemical Industry and John Wiley & Sons, Ltd

In this study, commercial surfactants have been investigated at economically viable dosage to enhance the enzymatic saccharification of pretreated wheat straw at high solid loadings. Twenty one surfactants were evaluated with pilot scale pretreated wheat straw and mechanism of surfactant action has been elucidated. One surfactant has improved the saccharification of dilute acid wheat straw (DAWS) by 26.4% after 24 h and 23.1% after 48 h while, steam exploded wheat straw (SEWS) saccharification was increased by 51.2% after 24 h and 36.4% after 48 h at 10% solid loading. At 20% solid loading, about 31% increase in yield was obtained on DAWS and about 55% on SEWS after 48 h. Further, lignin was isolated from pretreated wheat straws and characterized which revealed that SEWS derived lignin was more hydrophobic than DAWS lignin. This investigation suggests that surfactant supplementation during saccharification is an effective strategy to achieve higher saccharification yield.

Co-culture of fungal strains Penicillium janthinellum EMS-UV-8 (E), Penicillium funiculosum strain P (P) and Aspergillus sp. strain G (G) and blending of their crude cellulase were evaluated for improvements in cellulase activities as well as for enhanced hydrolysis of dilute acid pretreated wheat straw (PWS). The blending of crude enzymes of P and E enhanced the hydrolysis of PWS more effectively due to synergism in cellulolytic enzyme activities. Here, three types of blends were made on the basis of equal FPUs, equal protein content or fixed volume containing different proportions of individual enzymes, the former blend hydrolyzed 42.6% of PWS due to the 98%,62%, 64% and 34% synergistic enhancement in endo-glucanase, cellulase (FPU), β-glucosidase and xylanase activities, respectively. Hydrolysis at 10% solid loading of PWS in roller bottle reactor with this blend further enhanced hydrolysis yield to 74% within 24 h, which was much better than the corresponding hydrolysis yields of individual (38.1% by E and 61.5% by P) or the commercial enzyme (62.3%). This study proved that synergistic blends of cellulases from two Penicillium spp. are cost-effective tools for efficient wheat straw hydrolysis for on-site biofuel production.

Disaccharides or their derivatives were analyzed for the induction of cellulases by Penicillium janthinellum EMS-UV-8 mutant. Among seven (Crocin, Gentiobiose, Cellobiose, α-D-Cellobiose octaacetat...

Enzymatic hydrolysis at high solids loading has the potential to reduce both capital and operational expenditures. Here, pretreatment of rice straw (PRS) with dilute acid was carried out at a pilot scale (250 kg per day) at 162°C for 10 min and 0.35% acid concentration, followed by enzymatic hydrolysis at different total solids loadings. It showed that although the total sugar concentration increased from 48 to 132 g/l, glucan conversion reduced by 27% (84–66.2%) with increasing solids from 5 to 20% in batch mode. Therefore, two different fed-batch approaches were evaluated to improve the glucan conversion by the sequential addition of a substrate and/or enzyme. At 20% solid loadings and a 3 filter paper units/g enzyme dosage, the highest glucan conversion obtained was 66% after 30 h of hydrolysis in batch mode. However, in an optimized fed-batch approach, the glucan yield was improved to 70% by simply dividing the substrate feeding into three batches, that is, 50% at 0 h, 25% each after 4 h, and 8 h of hydrolysis reaction. The addition of surfactant (Ecosurf E6) further improved the conversion to 72% after 30 h. The role of critical factors, that is, inhibitors, enzyme–lignin binding, and viscosity, was investigated during the course of hydrolysis in the batch and fed-batch approaches. This study suggests a sustainable approach for improved hydrolysis at high solids loadings by fine-tuning a simple process.

Multiple enzymes are required for efficient hydrolysis of lignocellulosic biomass and no wild type organism is capable of producing all enzymes in desired levels. In this study, steam explosion of wheat straw was carried out at pilot scale and a synthetic enzyme mixture (EnzMix) was developed by partially replacing the cellulase with critical dosages of commercially available accessory enzymes (β-glucosidase, xylanase and laccase) through central composite design. Highest degree of synergism (DS) was observed with β-glucosidase (1.68) followed by xylanase (1.36). Finally, benchmarking of EnzMix (Celluclast, β-glucosidase and xylanase in a protein ratio of 20.40: 38.43: 41.16, respectively) and other leading commercial enzymes was carried out. Interestingly, hydrolysis improved by 75% at 6 h and 30% at 24 h, respectively in comparison of control. By this approach, 25% reduction in enzyme dosage was observed for obtaining the same hydrolysis yield with opitimized enzyme cocktail. Thus, development of enzyme cocktail is an effective and sustainable approach for high hydrolysis efficiency.

There is tremendous potential of plant growth-promoting rhizobacteria (PGPR) in the development of agriculture in a sustainable manner. PGPR live in a close association with plants and help in promoting their growth either directly or indirectly. Efficient PGPR detection in a quick and reliable manner is the need of the hour for their judicious implementation in improving the agriculture yields. Here, a recent up-to-date overview of the PGPR detection methods with a focus on novel immunobased tools and techniques for PGPR detection is presented. The immunobased techniques provide a cost-effective, fast, and highly specific alternative for PGPR detection. This study has implication in developing better understanding for the suitable methods of PGPR detection as per the needs of the research application.

Rhizosphere had a complex dynamic ecological relationship of plant and microbe. They are involved in the secretion of wide array of chemicals that can be classified as signaling compounds, antipathogenic compounds, growth regulators, and nutrient solubilizers. Thus, unraveling these interactions and the chemicals involved in these bilateral signaling can enable us to have a sustainable agriculture. Recently, ultrahigh-throughput techniques offered the potential to explore these interactions in holistic manner. Transcriptomics and metabolomics have led to novel investigations on plant development and stress responses. Additionally, these techniques had changed scenario of PGPR and biocontrol studies that previously involved single-aspect studies through traditional techniques. In this chapter, we summarize the aspects of rhizosphere metabolite studies including their potential challenges and opportunities.

Study describes the production of cellulases by Penicillium janthinellum EMS-UV-8 using untreated wheat straw (WS), treated WS (acid, alkali, steam exploded, organo-solv) and pure cellulosic substrates (avicel, cellulose-II and carboxymethyl cellulose). Severely pretreated WS and cellulose-II produced more cellulolytic enzymes than untreated samples. XRD and FTIR analysis revels that the increase in the amorphous structure of pretreated WS/cellulose increases enzyme production. Enzyme samples prepared using different substrates were used for the hydrolysis of dilute acid treated wheat straw (DATWS), steam exploded wheat straw (SEWS) and avicel. The enzyme prepared using untreated WS gave more hydrolysis of DATWS and SEWS than the enzyme prepared using pretreated WS or pure cellulosic substrates. This revels that more diverse/potential enzymes were secreted by P. janthinellum EMS-UV-8 mutant using untreated WS. This study may contribute in production of efficient enzyme mixture/cocktail by single fungal strain for economic conversion of biomass to sugars.

Conversion of pretreated lignocellulosic biomass (LCB) into sugars is one of the critical steps for bioethanol production. High LCB hydrolysis could be achieved by employing robust enzymes having high inhibitor tolerance, low irreversible lignin binding, and low end-product inhibition. In this study, acid pretreatment of wheat straw was carried out at pilot scale (250 kg/day) and three commercial cellulase preparations from Advanced Enzyme (AD), Novozyme (CL), and Genencor (AC) were evaluated for inhibitor (lignin, furfural, hydroxyl methyl furfural, vanillin) tolerance. Pretreated wheat straw (PWS) hydrolysis was carried out at different enzyme concentrations (1–30 mg protein/g of PWS) under optimum pH and temperature in rolling bottle reactor. Simultaneous saccharification and fermentation was performed employing in-house thermotolerant Saccharomyces cerevisiae . Results indicated that, maximum saccharification (more than 85%) was achieved at low protein loadings (10–15 mg protein/g PWS) of CL and this enzyme was also found to be more robust in presence of inhibitors. Maximum ethanol yield (78%) was found at 20 mg protein/g of PWS using CL. This study suggests that inhibitors have significant detrimental effect on enzymes and better understanding of enzyme-inhibitor correlation with its critical moderation would help in further enhancing the LCB hydrolysis at low enzyme dosage.

Second-generation bioethanol production by a newly isolated thermotolerant yeast strain was studied at 42 °C and above using pilot-scale dilute acid pretreated wheat straw (WS) as feedstock. This strain was identified as Kluyveromyces marxianus DBTIOC-35 by biochemical characterization as well as molecular phylogenetic analysis of the ITS-5.8S rRNA gene and D1/D2 domain of the 26S rRNA gene after PCR amplification and sequencing. Simultaneous saccharification and fermentation (SSF) at 42 °C and 45 °C using 10% biomass loading resulted in ethanol titers of 29.0 and 16.1 g L−1, respectively. At 42 °C ethanol productivity was higher during SSF (0.92 g L−1 h−1) than separate hydrolysis and fermentation (SHF) (0.49 g L−1 h−1) at 20% biomass loading. The results indicated that at 20% biomass loading, SSF without pre-saccharification led to more ethanol production (66.2 g L−1 with 83.3% yield) at a faster rate than SSF with pre-saccharification (PSSF) which produced an ethanol titer of 61.8 g L−1, 77.7% yield and productivity of 0.86 g L−1 h−1. Based on these findings, application of newly isolated yeast K. marxianus DBTIOC-35 in SSF of lignocellulosic biomass can eliminate the pre-saccharification step which is a novel advantage of thermotolerant yeasts in terms of cutting down the overall biomass to bioethanol process time and enhancing bioethanol titer, yields and productivities.

Requirement of high enzyme dosage for lignocellulosic biomass hydrolysis is one of the challenges for the viability of the second generation bioethanol technology. Here, an optimal enzyme mixture was developed by partially replacing the cellulase proportion with accessory enzymes (β-glucosidase, xylanase, pectinase, laccase) and its hydrolytic performance was compared with different commercial counterparts for the saccharification of pretreated wheat straw (PWS) using a 250 kg per day continuous pilot plant. Maximum degree of synergism was observed with xylanase followed by pectinase, laccase, and β-glucosidase. The statistically optimized enzyme mixture enhanced hydrolysis by 51.23% and 40.66% in 6 h and 24 h, respectively. This study elucidates that presence of even small amount of oligomers and cellobiose pose a strong inhibition for the enzymes. Therefore, development of an optimal enzyme formulation is a sustainable approach to reduce overall enzyme loading for biomass saccharification.

Indian biofuel research and development is increasing day by day. Indian government made a plan to make 20% ethanol/biofuel blending by 2020. Few companies are already working on the biodiesel/lignocellulosic ethanol research and production, but they are not yet commercially working. The ethanol from molasses is available only for making 5% blending with gasoline, and appropriate policies are necessary to increase the ethanol production not only from one source but from other various renewable resources. Research institutions are working to make lignocellulosic biofuels available at lower price. The production and use of biofuel not only helps India at economic level but also may help to reduce some greenhouse gas emissions. At present, India is one of the most CO2-emitting countries but behind the USA and China. The recent report indicates the slowdown of global CO2 emission and that may be because of several reasons, but it is a good beginning.

The bioethanol production from lignocellulosic biomass has attracted wide interest globally in last decade. One of the main reasons for the high cost of bioethanol production from lignocellulosic biomass is the expensive enzymes involved in enzymatic hydrolysis of cellulose (cellulase). The utilization of agro-industrial waste as a potential substrate for producing enzymes may serve a dual purpose of reducing the environmental pollution along with producing a high value commercial product. Twelve different agro-industrial wastes were evaluated for extracellular cellobiose or β-glucosidase production by a mutant of Bacillus subtilis on solid state fermentations (SSF). The Citrus sinensis peel waste was found to be the most suitable substrate with highest BGL titre (35 U/gds). Optimum incubation time, inoculum size, moisture content and volume of buffer for enzyme extraction were 72 h, 40 % v/w, 10 mL and 20 mL respectively.

The extracellular β-glucosidase from microorganisms is generally produced in low levels. Therefore, in this study, a β-glucosidase hyperproducing mutant was developed by multiple exposures of ethyl methyl sulfonate (EMS) and ultraviolet (UV) radiation (both individually and jointly) to Bacillus subtilis strain (PS). The developed mutants were screened, selected and characterized. The mutant, PS-UM1 developed after UV exposure alone, indicated a small increase in β-glucosidase production (718 U/l) in comparison to the wild-type strain, PS (675 U/l). The mutant, PS-CM5 developed after EMS exposure alone, displayed a slightly better production (762 U/l) than both the above strains. However, after exposure of the wild-type strain to both UV and EMS mutagens jointly, a better mutant (PS-CM5-UM3) was developed with 1.2-fold increase in production (806 U/l). Further, optimization of culture conditions by classical “one-variable-at-a-time” approach was done to determine the optimum, pH, temperature and nitrogen sources. The selected mutant (PS-CM5-UM3) produced up to 1,797 U/l enzyme and was found to be stable for ten generations. The β-glucosidase from the selected mutant (PS-CM5-UM3) was concentrated and purified using ammonium sulfate, dialysis and size-exclusion chromatography. The enzyme displayed maximal activity at 60 °C and it was found to be fairly stable at temperatures up to 70 °C for 30 min. Its molecular weight was determined to be around 60 kDa by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE).

Plant growth-promoting rhizobacteria (PGPR) pseudomonads have a large number of lipopolysaccharides on the cell surface, which induces immune responses. Cd-resistant PGPR prevalent at the Cd-affected sites under biophytostabilization was monitored. Transmissiom electron microscopy was used to the study the behavior of tolerance of PGPR to cadmium level and its effect on pseudomonad strains (Z9, S2, KNP2, CRPF, and NBRI). An immunosensor was developed by immobilizing antibody (anti-Z9 or anti-S2) against selected PGPR on a piezoelectric quartz crystal microbalance (QCM). Immunosensors were found to supplement the inherent specificity of antigen-antibody reactions with the high sensitivity of a physical transducer. On comparison of the efficiency of detection with ELISA, the spectrophotometric technique, the developed immunosensor was found to be more sensitive, fast, and reliable even after regeneration for several times. Thus, the immunosensor may be used for future detection of PGPR strains after automation of the screening process.

Superparamagnetic iron oxide nanoparticles (SPION) with size ranging 10.6–37.8 nm were synthesized and characterized through XRD, FT-IR spectra, simultaneous TG-DTG-DTA, vibrational sample magnetometry (VSM) and transmission electron microscopy (TEM). Effect of SPION size variants on the growth-profile of Low-Density Polyethylene (LDPE) degrading microbial consortium consisting of Microbacterium sp., Pseudomonas putida and Bacterium Te68R was monitored in Minimal broth Davis medium lacking iron and dextrose. Besides accelerating the bacterial growth, these nanoparticles also improved the exponential phase durability by 36 h. Further, shifting in lag-phase and the additive effect of sonication was also documented on growth profiling. SPION of size 10.6 nm were selected and were found to significantly increase the biodegradation efficiency of consortium as revealed by λ-max shifts, Fourier transform infrared spectroscopy (FT-IR) and simultaneous thermogravimetric-differential thermogravimetry-differential thermal analysis (TG-DTG-DTA). The study highlights the significance of bacteria–nanoparticle interactions which can dramatically influence key metabolic processes like biodegradation.

A total of six bacterial isolates were developed into two consortia and tested for utilization of epoxy silicone blends (ESBs; % w/w: 3.0) and epoxy as the sole carbon source. In-vitro biodegradation studies in minimal broth revealed that higher biomass and more sustained growth of consortia were obtained in the presence of epoxy and/or ESBs when these were incubated under aerobic conditions for 15 days. Treated samples were analyzed by Fourier transform infrared spectroscopy (FTIR) and simultaneous thermogravimetric–differential thermogravimetry–differential thermal analysis (TG–DTG–DTA), which indicated the breakage and formation of bonds in the polymer backbone. Moreover, a weight loss of 34.17 and 36.9% was found in epoxy and ESBs, respectively after 15 days of treatment with consortium-1. Further, in-vitro growth statistics study revealed more CFU count at mid-logarithmic phase in the presence of epoxy/ESBs unlikely to the absence of the polymers. However, the generation time was not affected. In the present study, consortium-1, comprising of Microbacterium sp., Pseudomonas putida and Bacterium Te 68R showed better biodegradation in comparison to consortium-2, wherein, P. putida and Pseudomonas aeruginosa were present. Overall, these results suggest that epoxy/ESBs polymers could be degraded by a biologically mediated process if a suitable consortium is used.

Jatropha curcas has been considered as a material of choice in India for the production of bio-diesel and a very large area has been planted in India. For better growth, Jatropha plants need extensive pruning once a year, and the pruning of a healthy two year old plant on an average gives about 4–6 kg of lignocellulosic material (LCM). Jatropha prunings can be available in significant amount on annual basis. These prunings have no other use and this material has potential to be an economical and suitable LCM for conversion to fermentable sugars, as these contain considerable amount of holocellulose. In this study, acid pretreatment of Jatropha pruning was carried out using dilute sulfuric acid. A wide range of variables, i.e., acid concentrations from 2.50% to 10.0%, temperature from 120 to 180 °C, and reaction time of 5–45 min were studied. Three response factors, namely, maximum xylose release, minimum inhibitors, and maximum enzymatic digestibility, were optimized by application Taguchi design. Pretreatment efficiency was determined by enzymatic saccharification and physico-chemical properties of both native and pretreated biomass analyzed using scanning electron microscopy and Fourier transform infrared spectroscopy. This study provides insights into the intricacies involved in conversion of this biomass to fermentable sugars. These studies indicate that Jatropha prunings can be converted economically into ethanol and can provide additional support to Jatropha based bio-diesel programme.