Promising Carbon Source Research Articles

Synthesis of isobutanol using acetate as sole carbon source in Escherichia coli

BackgroundWith concerns about depletion of fossil fuel and environmental pollution, synthesis of biofuels such as isobutanol from low-cost substrate by microbial cell factories has attracted more and more attention. As one of the most promising carbon sources instead of food resources, acetate can be utilized by versatile microbes and converted into numerous valuable chemicals.ResultsAn isobutanol synthetic pathway using acetate as sole carbon source was constructed in E. coli. Pyruvate was designed to be generated via acetyl-CoA by pyruvate-ferredoxin oxidoreductase YdbK or anaplerotic pathway. Overexpression of transhydrogenase and NAD kinase increased the isobutanol titer of recombinant E. coli from 121.21 mg/L to 131.5 mg/L under batch cultivation. Further optimization of acetate supplement concentration achieved 157.05 mg/L isobutanol accumulation in WY002, representing the highest isobutanol titer by using acetate as sole carbon source.ConclusionsThe utilization of acetate as carbon source for microbial production of valuable chemicals such as isobutanol could reduce the consumption of food-based substrates and save production cost. Engineering strategies applied in this study will provide a useful reference for microbial production of pyruvate derived chemical compounds from acetate.

Synthesis and formation mechanism of pitch-based carbon foam for three-dimensional structural applications

Carbon foam is a three-dimensional porous, rigid, and permeable material with applications in many fields owing to its excellent electrical and thermal properties. Pitch is a promising carbon source for carbon foam production, and its modification with nitric and sulfuric acids has been widely investigated. However, the foaming phenomenon resulting from the acid treatment of pitch and the resultant formation of porous structures remain poorly understood. Herein, we clarified the mechanism by which the porous structure of pitch-derived carbon foam is formed by analyzing the components of pitch modified by nitric acid treatment and identifying essential conditions for foam production. Carbon foam was obtained by pitch modification at a high concentration of nitric acid (60 wt%), whereas no carbon foam was formed at low nitric acid concentrations (<60 wt%). Furthermore, at high nitric acid concentrations, carbon foam formation proceeded at a relatively low temperature (280 °C). The formation of carbon foam from modified pitch was attributed to the synergistic effect of the functional groups introduced onto pitch and the low-molecular-weight components resulting from cracking. This work provides new insights into pitch as a precursor and provides a straightforward method for producing carbon foam.

Self-Hydrogen Supplied Catalytic Fractionation of Raw Biomass into Lignin-Derived Phenolic Monomers and Cellulose-Rich Pulps.

Lignocellulosic biomass is one of the most well-studied and promising green carbon sources. The fullest utilization of lignocellulosic biomass in hydrogen-free and mild conditions to produce phenolic monomers while preserving cellulose-rich pulps is challenging and has far-reaching significance. Here, we report an innovative strategy to convert lignocellulosic biomass into lignin oils and cellulose-rich pulps without exogenous hydrogen under mild conditions over a Pt/NiAl2O4 catalyst. In this process, the structural hydrogens in hemicellulose acted as a hydrogen source to realize the fractionation and depolymerization of lignin into phenolic monomers while keeping the cellulose intact, which is named self-hydrogen supplied catalytic fractionation (SCF). By using water as a solvent, the theoretical yield of phenolic monomers (46.6 wt %, with propyl(ethyl) end-chained syringol and guaiacol as main products) is achieved at 140 °C for 24 h, with 90% cellulose intact in birch sawdust. This H2-free process can be extended to other biomass (hardwood, softwood, and grass) and can be scaled up. The Pt/NiAl2O4 catalyst also shows good stability in recycling as well as regeneration treatment. This work provides a new strategy to achieve high utilization of lignocellulosic biomass for sustainable biorefinery by using water as a solvent without exogenous hydrogen under mild conditions.

Biomass waste fern leaves as a material for a sustainable method of activated carbon production for CO2 capture

In this work, we report the use of activated carbon synthesized from a sustainable material - fern leaves - as a sorbent for carbon dioxide capture applications. The resource-friendly technology for activated carbon production was applied and described. The activated carbons were prepared by chemical and physical activation and carbonization at the same time at the temperature range of 500–900 °C. This method reduces energy consumption and resources. KOH and CO2 were used as activating agents. The evaluation of the CO2 adsorption ability of the activated carbon was supported by different methods including: elemental analysis using X-ray fluorescence spectroscopy, ash content, surface area and porosity measurements, Raman spectroscopy, X-ray spectroscopy and scanning electron microscopy. Results indicated that the optimum temperature of the synthesis was 700 °C. The highest achieved adsorption of CO2 was equal to 6.77 mmol/g and 3.58 mmol/g at 0 °C and 25 °C, respectively. The activated carbons synthesized from fern leaves showed high CO2 adsorption and selectivity. Moreover, the abundance and low cost of fern leaves make them very promising carbon sources for CO2 sorbents production.

Co2SiO4/CoO heterostructure anchored on graphitized carbon derived from rice husks with hierarchical pore as electrode material for supercapacitor

Biomass is treated as the most promising carbon source for supercapacitor electrodes. However, ash in biomass especially Si component is always identified as an adverse substance, which is moved by acid pickling in advance. Factually, SiO2 in biomass can be converted into transition metal silicate (TMS). In this work, NaH2PO2 and Co(NO3)2 are newly used in sequence to form mesopores and micropores on the rice husks which can be regarded as one carbon-silicon compound material. SiO2 in rice husks is converted to TMSs reacting with Co(NO3)2, and carbon is catalyzed to graphitize by the Co element. The remaining CoO derived from Co(NO3)2 forms a heterostructure with Co2SiO4. The pore design criteria for electrode materials with redox reactions are proposed based on COMSOL simulation results, which include mesopores playing a decisive role in ion diffusion, the pore size should be gradually reduced, and the specific capacitance is significantly increased when the porosity is greater than 0.8. The electrode material prepared that Co2SiO4/CoO is anchored on carbon with hierarchical pores has outstanding performance: 246.60 F·g−1 at 0.5 A·g−1 for specific capacitance and good cycle capability (88.06% after 10,000 cycles). For the mr10-500-C/CoSi/CoO-900//AC device, it has excellent energy density (37.500 Wh·kg−1 at 1350 W·kg−1).

Organic matter release characteristics of brown rice: A promising solid carbon source with unique dual-enzyme system for wastewater treatment

Solid carbon source (SCS) has attracted increasing research interests considering its merits of sustainable organic matter release capacity, safe transportation, easy management, and no need for frequent addition. In this study, the organic matter release capacities of five selected natural (milled rice and brown rice) and synthetic (PLA, PHA, PCL) SCSs were systematically investigated. The results showed that brown rice was the preferable SCS with high COD release potential, release rate and maximum accumulation of 309.2 mg-COD/g-SCS, 581.3 mg-COD/L·d and 6183.3 mg-COD/L, respectively. The cost for COD supply of brown rice stood at $1.0/kg-COD with considerable economic viability. The organic matter release process of brown rice could be well depicted by Hixson-Crowell model with a rate constant of −1.10. The addition of activated sludge could enhance the organic matter release of brown rice, evidenced by the increased release of VFAs with a proportion up to 97.1 % in the total organic matter. Moreover, the mass flow of carbon showed that the addition of activated sludge could improve the carbon utilization rate, and the peak value could achieve 45.4 % in 12 days. The unique dual-enzyme system, consisting of exogenous hydrolase from microorganisms in activated sludge and the endogenous amylase from brown rice, was supposed to be the main reason for the superior carbon release capacity of brown rice over other SCSs. This study was expected to offer an economic and effective SCS for the biological treatment of low-carbon wastewater.

Study on the Structure and Bioactivity of Ganoderma lucidum Polysaccharides under Cassava Stalk Stress.

Various carbon sources affect the growth of the G. lucidum fruiting body, and the cassava stalk is considered a promising carbon source for G. lucidum. The composition, functional group characteristics, molecular weight distribution, antioxidant activity in vitro, and growth effect of L. rhamnosus LGG of G. lucidum polysaccharides (GLPs) under cassava stalk stress were investigated by gas chromatography-mass spectrometry, near-infrared spectroscopy, and gel chromatography. The results showed that GLPs consisted of D-glucose, D-galactose, and seven other monosaccharides. The end of the sugar chain had β-D-Glc and β-D-Gal configurations. The total sugar content in GLP1 was the highest (4.07%), and GLP1, GLP2, GLP3, and GLP5 had the β-D-Gal configuration, while GLP4 and GLP6 had the β-D-Glc configuration. The greater the proportion of cassava stalk, the greater the maximum molecular weight of GLPs. The total antioxidant capacities of GLPs obtained from different cassava stalks significantly varied, as well as their stimulating effects on the L. rhamnosus LGG growth. Higher concentrations of GLPs corresponded to the more intensive growth of L. rhamnosus LGG. This study provided essential data support for cassava stalk as a carbon source in G. lucidum cultivation.

One-step strategy of 3D hierarchical porous carbon with self-heteroatom-doped derived bread waste for high-performance supercapacitor

Bio-waste is a promising carbon source that can be used as a basic component in renewable supercapacitors due to its abundant hierarchical pore structure potential, heteroatom self-doping capability, high surface area, as well as well-defined chemical and mechanical stability. This study converted bread bio-waste into rich 3D hierarchical porous carbon through a one-step facile strategy to be used as the main component of a supercapacitor. The porous carbon was obtained through physical activation approach at different temperatures of 750, 800, 850, and 900 °C without being combined with chemical activation. The optimized activated carbon illustrated high porosity behavior with an abundant 3D hierarchical pore structure consisting of 76.98% micropores and 23.02% mesopores and also produced a well-defined wettability of self-doping heteroatoms. Moreover, the electrochemical behavior in a symmetric supercapacitor cell showed a high specific capacitance of 202 F g−1 at 1 A g−1 with a rate capability of 73% at 10 mV s−1 in a 1 M H2SO4 electrolyte. It was also discovered that the activation temperature of 850 produced the highest energy density of 11.61 Wh kg−1 at a power density of 156.71 W kg−1 with a low equivalent series resistance of 0.11 Ω. Finally, the proof-of-concept showed that bread waste has immense potential as a 3D hierarchical porous carbon source after the synthesis through a single-stage facile approach and can be used as a major renewable electrode component for sustainable supercapacitors.

Development of a novel methanotrophic platform to produce ectoine from methane and lignocellulose-derived sugars

Methane is considered a promising carbon source in the field of biotechnology. Using methane as the carbon source for producing chemicals reduces manufacturing costs and tackles the issue of global warming. Like methane, lignocellulose biomass is also an inexpensive and ample carbon source, which could be used for industrial biomanufacturing. In this study, Methylotuvimicrobium alcaliphilum 20Z was genetically modified to simultaneously consume methane and lignocellulose-derived sugars (glucose and xylose) to produce ectoine, a native osmoprotectant. The xylose utilization pathway, comprising xylA (xylose isomerase) and xylB (xylulokinase) genes from Escherichia coli, was first integrated into the chromosome of M. alcaliphilum 20Z. Further expression of the glucose utilization, consisting of glf (glucose facilitator) from Zymmonas mobilis, glk (endogenous glucokinase), and pgi (glucose 6-phosphate isomerase) from E. coli, made the engineered strain 20ZXG consume methane, xylose, and glucose concurrently. Cultivation on three substrates upregulated the Embden–Meyerhof–Parnas and ectoine biosynthesis pathways of 20Z. As a result, the ectoine content produced by 20ZXG grown on the three substrates was 1.7-fold enhanced compared with that obtained on methane solely. Furthermore, the knock-out of ectoine biosynthesis repressor (ectR1) led to an output of 37.93 ± 3.27 mg/g-DCW, which was the highest quantity of ectoine produced after 48 h of cultivation in the presence of three substrates and was 2.3-fold higher than the initial output.

Adaptive laboratory evolution to hypersaline conditions of lactic acid bacteria isolated from seaweed

Seaweed biomass has been proposed as a promising alternative carbon source for fermentation processes using microbial factories. However, the high salinity content of seaweed biomass is a limiting factor in large scale fermentation processes. To address this shortcoming, three bacterial species (Pediococcus pentosaceus, Lactobacillus plantarum, and Enterococcus faecium) were isolated from seaweed biomass and evolved to increasing concentrations of NaCl. Following the evolution period, P. pentosaceus reached a plateau at the initial NaCl concentration, whereas L. plantarum, and E. faecium showed a 1.29 and 1.75-fold increase in their salt tolerance, respectively. The impact that salt evolution had on lactic acid production using hypersaline seaweed hydrolysate was investigated. Salinity evolved L. plantarum produced 1.18-fold more lactic acid than the wild type, and salinity evolved E. faecium was able to produce lactic acid, while the wild type could not. No differences in lactic acid production were observed between the P. pentosaceus salinity evolved and wild type strains. Evolved lineages were analyzed for the molecular mechanisms underlying the observed phenotypes. Mutations were observed in genes affecting the ion balance in the cell, the composition of the cell membrane and proteins acting as regulators. This study demonstrates that bacterial isolates from saline niches are promising microbial factories for the fermentation of saline substrates, without the requirement of previous desalination steps, while preserving high final product yields.

Effect of thermal hydrolyzed sludge filtrate as an external carbon source on biological nutrient removal performance of A2/O system

Thermal hydrolyzed sludge filtrate (THSF) rich in biodegradable organics could be a promising external carbon source for biological nutrient removal (BNR). The use of THSF can effectively reduce wastewater treatment plants operating costs and recover bioresources and bioenergy from the waste activated sludge. In this study, the effect of THSF on the BNR process was investigated using a lab-scale anaerobic/anoxic/oxic (A2/O) system. Total nitrogen (TN) and total phosphorus (TP) removal efficiencies of 74.26 ± 3.36% and 92.20 ± 3.13% at a 0.3% dosing ratio were achieved, respectively. Moreover, 20.42% of the chemical oxygen demand (COD) contained in THSF contributed to denitrification, enhancing nitrogen removal efficiency from 55.30 to 74.26%. However, the effluent COD increased by approximately 36.80%, due to 18.39% of the COD contained in THSF discharged with effluent. In addition, the maximum denitrification rate was approximately 16.01 mg N g VSS-1 h-1, while the nitrification rate was not significantly affected by THSF. Nitrosomonas, a common chemoautotrophic nitrifier, was not detected after the introduction of THSF. The aerobic denitrifier Rubellimicrobium was stimulated, and its relative abundance increased from 0.16 to 3.03%. Moreover, the relative abundance of Dechloromonas was 3.93%, indicating that the denitrifying phosphorus removal process was enhanced. This study proposes an engineering application route of THSF, and the chemical phosphate removal pretreatment might be a means to suppress the phosphate recirculation.

Corncob as Carbon Source in the Production of Xanthan Gum in Different Strains Xanthomonas sp.

Xanthan gum (XG) is a biopolymer obtained in fermentation and used as a rheology control agent in aqueous systems and in stabilizing emulsions and suspensions. XG, together with other polysaccharides, can form soft, cohesive composite gels. The carbon source in the fermentative process is responsible for one-third of the production costs, and the search for less expensive and sustainable alternatives is ongoing. The use of agricultural residues such as the corncob is highly suggestive due to their abundance. This study aims to evaluate the use of derived hemicellulose fractions from the alkaline extraction of corncob as a carbon source in the production of XG in trials using four strains of Xanthomonas sp. (629, 1078, 254, and S6). The results indicate that strain 629 provides the higher yield (8.37 ± 5.75 g L−1) while using a fermentation medium containing a carbon source of saccharose (1.25%), hemicellulose fractions (3.75%), and salts. In this same medium, the strain 629 produces gum in 3% aqueous solution, showing the higher apparent viscosity (9298 ± 31 mPa s−1) at a shear rate of 10 s−1 at 25 °C. In conclusion, corncob is proven to be a promising sustainable alternative carbon source in the obtention of XG, improving the economic viability of the process within a biorefinery context. Saccharose must, however, also be included in the fermentation medium.

Evaluation of the biosynthesis, structural and rheological characterization of succinoglycan obtained from a formulation composed of whole and deproteinized whey

In this study, succinoglycan was produced from whey and its rheological and structural characteristics were elucidated. Eight culture media were prepared with different ions for bioconversion of whey into succinoglycan. The formulation composed of deproteinized whey, monobasic potassium phosphate and magnesium sulfate allowed the production of 13.7 ± 0.43 g/L of succinoglycan. The apparent molar mass of succinoglycan was estimated to be 9.033 × 105 g/mol and the polydispersity index was 1.044, representing the homogeneity of the sample. Monosaccharide composition of glucose and galactose for the succinoglycan produced was 6.6:1.0. The 1H RMN analysis revealed the non-saccharide substituent content of 1.2%, 3.0% and 8.1% for acetyl, succinate and pyruvate, respectively. The rheological results showed that the apparent viscosity of the succinoglycan solutions was directly proportional to the concentration, and the solution showed pseudoplastic behavior. Dynamic frequency sweep tests identified that a concentration of 2.0% of succinoglycan is required for formation of the gel system. Temperature influenced the viscoelastic behavior of succinoglycan and revealed the melting point and reversibility of the gel. Whey was shown to be a promising carbon source for the production of succinoglycan with thickening potential and viscosity modifier.

Optimization of bacterial cellulose production from prickly pear peels and its ex situ impregnation with fruit byproducts for antimicrobial and strawberry packaging applications

Bacterial cellulose (BC) is currently among the most promising natural polymers. However, the production costs and biological inactivity are still challenges. The current study exploited the enzymatically hydrolyzed prickly pear peels (PPP) for BC production, which supported about 2.94 g/L as the sole production medium. The BC production was further optimized through a central composite design, where the maximum BC production was 6.01 g/L at 68 % PPPE at pH 4 after 11 days of incubation at 20 °C. The produced BC was characterized by FT-IR spectroscopy, XRD, and SEM analysis, and the results showed that PPPE is a promising carbon source for pure BC production. The BC membrane was separately loaded with several fruit byproduct extracts to enhance its biological activity for multiple applications. BC loaded with pomegranate peel extract (BC/PPE) revealed significant broad-spectrum antimicrobial activity, followed by BC loaded with pomegranate molasses (BC/PM). The BC/PPE membrane enhanced the shelf-life storage of strawberry fruits by about 5 days, with a reduction in the fruits' weight loss of 15 % compared to the uncovered group. The current study revealed the successful application of PPE for sustainable BC production with its packaging potential for enhancing strawberry shelf-life when loaded with PPE or PM.

N/O co-doped micropores carbon derived from a solvent-free synthesized polymer for high-performance supercapacitor

BackgroundHeteroatom-doped porous carbons have attracted widespread concern as promising electrode materials for supercapacitors. Polymers are considered as the promising carbon sources because their derived carbons possess the unique advantages of inherited uniform heteroatoms doping, high purity, and good reproducibility. While the synthesis process of polymers usually involves solvents, which will bring a pollution of the environment and increase the consumption of cost and energy. MethodsHerein, nitrogen/oxygen co-doped porous carbons (NOPCs) with predominant micropores were prepared via carbonization and activation of a solvent-free synthesized polymer using 2-aminophenol, hexamethylenetetramine as monomers. Kinetics studies and density functional theory (DFT) simulations reveal that N/O heteroatoms credibly introduces pseudocapacitance and greatly improves the chemisorption of K+, leading to an outstanding electrochemical performance. Significant findingsThe obtained NOPCs exhibit interconnected microporous structure, large specific surface area (3297 m2 g−1), narrow pore size distribution (ca. < 1 nm), suitable heteroatoms content (N: 4.13%, O: 13.06%) and high carbon yield of 48 wt%. Benefitting from these features, the optimal NOPC-800 delivers a remarkable specific capacitance of 410 F g−1 at 1 A g−1 and retains 270 F g−1 at 50 A g−1. The solid-state micro-supercapacitors fabricated from the NOPCs presents areal capacitance up to 29.7 mF cm−2 and energy density up to 0.97 μWh cm−2.

Bioconversion of cellulose into bisabolene using Ruminococcus flavefaciens and Rhodosporidium toruloides

In this study, organic acids were demonstrated as a promising carbon source for bisabolene production by the non-conventional yeast, Rhodosporidium toruloides, at microscale with a maximum titre of 1055 ± 7 mg/L. A 125-fold scale-up of the optimal process, enhanced bisabolene titres 2.5-fold to 2606 mg/L. Implementation of a pH controlled organic acid feeding strategy at this scale lead to a further threefold improvement in bisabolene titre to 7758 mg/L, the highest reported microbial titre. Finally, a proof-of-concept sequential bioreactor approach was investigated. Firstly, the cellulolytic bacterium Ruminococcus flavefaciens was employed to ferment cellulose, yielding 4.2 g/L of organic acids. R. toruloides was subsequently cultivated in the resulting supernatant, producing 318 ± 22 mg/L of bisabolene. This highlights the feasibility of a sequential bioprocess for the bioconversion of cellulose, into biojet fuel candidates. Future work will focus on enhancing organic acid yields and the use of real lignocellulosic feedstocks to further enhance bisabolene production.

Optimization and kinetic modeling of media composition for hyaluronic acid production from carob extract with Streptococcus zooepidemicus.

Hyaluronic acid (HA), a mucopolysaccharide belonging to the glycosaminoglycan family, consists of repeating disaccharide units and has been used directly or indirectly in numerous human health practices. This study focused on evaluating carob pods for microbial HA production and kinetic modeling of HA fermentation. Therefore, the optimal medium composition was determined using Plackett-Burman Design (PBD) for HA production from carob extract with Streptococcus zooepidemicus. Maximum HA production of shake flask fermentation was 2.6g/L (1.25 × 106) in the optimum medium, comprising 10°Bx of carob pods extract, 0.5g/L of MgSO4.7H2O, 10.0g/L of casein, 2.5g/L of KH2PO4, 2.0g/L of NaCl, 1.5g/L of K2HPO4, 0.002g/L of FeSO4 and 10.0g/L of beef extract. In the continuation of the study, the fermentation performed with the optimal medium composition was modeled using three different models including the logistic model for biomass production, the Luedeking-Piret model for HA production, and the modified Luedeking-Piret model for substrate consumption. Based on the results, the experimental HA production data agreed with the Luedeking-Piret model with an R2 of 0.989. Since the α value was 63-fold higher than the value of β, the HA production is growth-associated. Consequently, carob extract can be evaluated as a promising carbon source for producing HA.

Box–Behnken Design Optimizing Sugarcane Bagasse-Based Nitrogen-Doped Carbon Quantum Dots Preparation and Application in Ferric Ion Detection

Sugarcane bagasse is an abundant biomass waste and a promising carbon source for preparing carbon-based materials such as carbon quantum dots (CQDs). Low quantum yield is a major problem for sugarcane bagasse-based carbon quantum dots. Heteroatom-doped modification is an efficient approach to improve the quantum yield. A facile hydrothermal carbonization method was applied to synthesize the nitrogen-doped carbon quantum dot N-CQDs using urea as the nitrogen source. The synthetic procedure was determined by the single-factor experiments and the response surface methodology (RSM) based on Box–Behnken design (BBD). The optical properties of optimized N-CQD-13 were more excellent than those of undoped CQD. Higher quantum yields (both absolute and relative) were observed in N-CQD-13. Additionally, N-CQD-13 exhibited high stability for long-time storage and excellent pH tolerance in aqueous solutions. N-CQD-13 were applied to detect Fe3+ in aqueous solutions with a low detection limit of 0.44 μM. The fluorescence lifetime decay of the N-CQD-13 solutions untreated and treated with Fe3+ indicated the probable involvement of a dynamic fluorescence-quenching mechanism. Thus, this work explored a reliable method for the high-quality utilization of bagasse.

Potential of food waste-derived volatile fatty acids as alternative carbon source for denitrifying moving bed biofilm reactors

Fossil-based materials such as methanol are frequently used in the denitrification process of advanced biological wastewater treatment as external carbon source. Volatile fatty acids (VFAs) produced by anaerobic digestion of food waste, are sustainable compounds with the potential to act as carbon sources for denitrification, reducing carbon footprint and material costs. In this study, the effectiveness of food waste-derived VFAs (AD-VFA) was investigated in the post-denitrification process in comparison with synthetic VFA and methanol as carbon sources. Acetic acid had the highest rate of disappearance among single tested VFAs with a denitrification rate of 0.44 g NOx-N removed/m2/day, indicating a preferential utilization pattern. While AD-VFA had a denitrification rate of 0.61 mg NOx-N removed/m2/day, sVFA had a rate of 0.57 mg NOx-N removed/m2/day, indicating that impurities in AD-VFA did not play substantial role in denitrification. AD-VFA proved to be promising carbon source alternative for denitrification in wastewater treatment plants.

Potential of indigenous ligno-cellulolytic microbial consortium to accelerate degradation of heterogenous crop residues.

Indigenous microbial diversity has potential for rapid decomposition of residue through enzyme activities that is alternative, effective, and environment friendly strategy to accelerate degradation of lignocellulose in agricultural residues and make composting process economically viable. Keeping this view, the main objective of the present study was isolation and characterization of lignocellulosic degrading microbial diversity from long-term residue management practice experiments and to develop potential microbial consortium for rapid degradation of lignocellulosic biomass. In this study, twenty-five bacteria, nine fungi, and four actinomycetes isolates were obtained from the soil samples of different residue management fields from Ludhiana, Punjab, India. All isolates were qualitatively and quantitatively screened for enzyme activities, i.e., cellulase, xylanase, laccase, and lignin peroxidase. On the basis of quantitative estimation of enzyme activities, 3 fungal (S1F1, S2F4, and S6F9), 2 actinomycetes (S1A1 and S6A4), and 2 bacterial strains (S6B16 and S6B17) were further selected for in vitro bio-compatibility assay. Selected bio-compatible microbial strains were identified as Streptomyces flavomacrosporus (S6A4), Aspergillus terreus (S2F4), and Bacillus altitudinis (S6B16) through 16S rRNA and 18S rRNA sequencing. Furthermore, single and developed microbial consortium (S6B16 + S6A4 + S2F4) were screened for quantitative estimation of cellulase, xylanase, laccase, and lignin peroxidase enzymes with 23 biochemically different cereal, legume, and oil seed crop residues for optimization of enzyme activities at different time intervals. Results revealed that Vigna radiata followed by Cajanus cajan and Arachis hypogaea straw residue powder @ 1% in culture broth are a promising carbon source for B. altitudinis, S. flavomacrosporus, and A. terreus to produce higher ligno-cellulolytic microbial degrading enzymes due to variable range of carbon (C):nitrogen (N) ratio and higher ligno-cellulolytic content in the studied crop residues. Thus, the application of indigenous microbial consortium with efficient lignocellulose hydrolysis enzyme machinery might be an attractive alternative for ex situ crop residue management practices under sustainable manners.