Search Results (641)

Cyanobacterial species in the Arabian Peninsula region display a diverse range of potential biotechnological application. This review summarizes the cyanobacteria diversity found in the Peninsula region, the bioactive compounds found in these species, and the several health benefits and applications. The Arabian Peninsula region comprises a wide range of cyanobacteria with representatives from the orders Oscillatoriales, Chroococcales, Stigonematales, and Nostocales. These microorganisms produce specialized metabolites such as photosynthetic pigments, pigment–protein complexes, lipopeptides, phenolic compounds, and unique secondary metabolites. Many of the metabolites offer beneficial biological functions including antioxidants, antibacterial, anti-cancer, anti-inflammatory antiviral, and neuroprotective ones. In addition to the medical-related practices, cyanobacteria in the Peninsula region might have several other applications. Other probable uses include their potential bioremediation capability to remove pollutants or heavy metals, as a potential biohydrogen source for renewable energy, and as biofertilizers and soil enhancement to support sustainable agriculture; other useful applications include bioplastics production (polyhydroxyalkanoates), soil microbiota improvement, and methane reduction. The review highlights the potential diverse biotechnological applications of Arabian Peninsula cyanobacteria toward bioremediation, bioplastics, ecosystem regeneration, biofertilizers, bioenergy, and agro-sustainability, as well as human health. This review highlights the importance of the further exploration and exploitation of these resourceful microorganisms for sustainable development in the Arabian Peninsula region. Full article

Microbial polyhydroxyalkanoates (PHAs) are biodegradable biopolymers that are gaining traction as replacements for conventional petroleum-based plastics. In this study, sugar utilization, growth and polyhydroxybutyrate (PHB) and polyhdroxyvalerate (PHV) production in synthetic and real hydrolysates of Canola fines (SHCF, RHCF) by Gordonia lacunae BS2^T were evaluated: (i) in SHCF under different C:N ratios and O₂ availability, and (ii) in SHCF and RHCF (50% and 100%) under shaking v/s static conditions with limited or non-limited O₂. The bacterium was able to utilize glucose, cellobiose, arabinose, and xylose. Athough O₂ limitation reduced growth, higher measured concentrations of 3-hydroxyvalerate (3HV) were achieved under O₂ limitation, translating into slightly higher 3-hydroxybutyrate (3HB)+3HV yields (15.4 ± 2.36 %wt.wt.) than under non-O₂ limited conditions (12.4 ± 2.26 %wt.wt.). Notably, 50% RHCF was the most suitable medium for growth and PHB+PHV production, while 100% RHCF was the least suitable. The 3HV+3PV concentration (0.35 g/L), 3HV fraction (24%), and yield (15.4 %wt.wt.) in 50% RHCF were highest under static, O₂-limited conditions, corresponding with negligible sugar utilization (1.6 mg/day.100 mL⁻¹ glucose) and suggesting alternative metabolic pathways using other substrates in the RHCF for growth. Nuclear magnetic resonance results indicated that Gordonia lacunae BS2^T produces a desirable co-polymer (PHBV), paving the way for ongoing research using this bacterium. Full article

Tropical lignocellulosic residues are increasingly relevant feedstocks for lignin-containing nanocellulose composites, but their performance cannot be predicted from botanical origin or bulk lignin percentage alone. This review defines the interface as the geometrical boundary between phases and the interphase as the finite, compositionally graded region in which lignin distribution, nanocellulose morphology, adsorbed water, and the surrounding matrix jointly govern stress transfer and mass transport. Using an evidence-weighted framework, the literature is organized into the following categories: residual-lignin nanofibrils, redeposited-lignin systems, lignin nanoparticle assemblies, compatibilized thermoplastic hybrids, and all-lignocellulosic sheets. Representative quantitative observations show that controlled residual lignin can the increase water contact angle from approximately 35 degrees to 78 degrees and reduce oxygen permeability by up to 200-fold in nanopapers, while selected PLA/LCNF systems show tensile-strength and modulus increases of 37% and 61%, respectively; however, high or poorly distributed lignin can suppress fibrillation, lower viscosity, weaken gel networks, and reduce reproducibility. The most defensible near-term product windows are packaging layers, grease/oil barrier papers, coatings, paper-like multilayers, and selected porous media. Thermoplastic matrices remain process-sensitive, and biomedical, additive-manufacturing, nano-reactor, and energy-material claims require stronger validation of the extractables, rheology, humidity history, TEA/LCA metrics, and end-of-life behavior. This review, therefore, provides a critical, application-backward roadmap for tropical biorefineries in which interfacial function, wet handling, drying energy, and process integration are assessed together rather than treated as independent variables. The abbreviations used in the abstract are defined as follows: CNFs, cellulose nanofibrils; CNC, cellulose nanocrystals; LCNF, lignin-containing cellulose nanofibrils; LCNCs, lignin-containing cellulose nanocrystals; PLA, poly(lactic acid); PHB, polyhydroxybutyrate; PHAs, polyhydroxyalkanoates; PVA, poly(vinyl alcohol); DESs, deep eutectic solvents; TEA, techno-economic analysis; LCA, life-cycle assessment; ML, machine learning. Full article

The valorisation of lignocellulosic residues into bio-based feedstocks is a key strategy for advancing circular bioeconomy models. In this study, chestnut wood residues, including virgin wood (VW) and detannized wood (DT) from the tannin industry, were evaluated as substrates for polyhydroxyalkanoate (PHA) production using Cupriavidus necator. Biomass was subjected to thermo-acid hydrolysis followed by ion-exchange detoxification, yielding hydrolysates rich in organic acids (levulinic, acetic, and formic acids) and residual inhibitory compounds. Both substrates supported microbial growth and PHA accumulation, although clear differences in performance were observed. The maximum biomass concentration reached 1.26 ± 0.01 g L⁻¹ in VW hydrolysate and 0.40 ± 0.03 g L⁻¹ in DT hydrolysate. PHA production was higher in VW hydrolysate, reaching 68.51 mg L⁻¹ with 5.44% (w/w) accumulation, while DT hydrolysate yielded 0.21 mg L⁻¹ with 6.01% (w/w). The reduced biomass formation in DT hydrolysate was associated with the greater persistence of inhibitory compounds generated during thermo-acid treatment. Although the obtained PHA yields are lower than those reported for optimized lignocellulosic systems, this study demonstrates for the first time the feasibility of producing PHA from chestnut wood residues, including industrial detannized byproducts, without nutrient supplementation. These findings highlight the potential of tannin-industry waste streams as alternative feedstocks for biopolymer production, while indicating that optimization of hydrolysis conditions, detoxification efficiency, and fermentation strategy is required to improve process performance. Full article

The growing accumulation of fossil-based plastic waste and the underutilization of organic residues from the agri-food sector highlight the need for alternative, low-impact material solutions. Polyhydroxyalkanoates (PHAs) represent a promising family of bio-based and biodegradable polymers; however, their large-scale deployment is still limited by economic and environmental constraints, strongly influenced by feedstock selection and processing requirements. In Mediterranean regions, orange peel waste (OPW) generated in large quantities by the citrus-processing industry may represent a valuable renewable input for the development of PHA-based biocomposites. In this study, a Life Cycle Assessment (LCA) was performed to evaluate a PHA-based composite reinforced with OPW, following established LCA principles and focusing on a residue-based valorization pathway. The analysis includes the collection and pre-treatment of OPW, PHA production from different feedstock matrices, composite manufacturing, and relevant downstream processing stages. The study aims to quantify the environmental implications of integrating OPW into PHA matrices, identify key hotspots, and support evidence-based material design within circular economy strategies. In addition, it assesses the feasibility of producing a PHA–OPW filament suitable for market-ready applications, developed in collaboration with Krill Design^®. Full article

The accumulation of petroleum-based plastics demands sustainable alternatives such as polyhydroxyalkanoates (PHAs), biodegradable polyesters synthesised by numerous prokaryotes. However, high feedstock costs limit their commercialisation. This study evaluated cocoa mucilage, an underutilised by-product of the Ecuadorian cacao sector, as a low-cost carbon source for PHA production by a wild-type strain isolated from cocoa fruit residues. Bacteria were recovered from cocoa mucilage and pod shell fractions and screened for PHA accumulation by Sudan Black B staining with UV–Vis spectrophotometric confirmation. A single PHA-positive isolate, designated Priestia aryabhattai strain NBP01-UTN (GenBank accession OR567321.1; 99.88% 16S rRNA gene sequence identity to the type strain B8W22T), was recovered from the cocoa shell surface—representing, to the best of our knowledge, the first report of a PHA-producing P. aryabhattai from cacao fruit residues. Fermentation conditions were optimised using the response surface methodology with a central composite design evaluating temperature, pH, and ammonium sulphate concentration. The fitted quadratic model was highly significant (R² = 0.978, p < 0.0001), indicating that temperature and nitrogen limitation were the dominant factors. Optimal conditions (40 °C, pH 7.30, 0 g·L⁻¹ (NH₄)₂SO₄) yielded 0.496 g·L⁻¹ PHA at 24 h (productivity ≈ 20.7 mg·L⁻¹·h⁻¹). Notably, no external nitrogen supplementation was required, as the endogenous nitrogen in cocoa mucilage sufficed to sustain growth whilst triggering the nutrient imbalance needed for PHA biosynthesis. FTIR and DSC analyses provided spectroscopic and thermal evidence consistent with poly(3-hydroxybutyrate) (PHB), although definitive monomer-level confirmation requires GC–MS or NMR spectroscopy. These results demonstrate the feasibility of coupling a locally isolated wild-type strain with cocoa mucilage to produce bioplastic within a circular bioeconomy framework. Full article

The use of bio-based and biodegradable plastic products (BBpPs) ensures the mitigation of environmental effects of fossil-based plastics, especially in humanitarian crises where waste management is challenging. Polyhydroxyalkanoates (PHAs) are promising biodegradable biopolymers that are biocompatible and do not cause microplastic pollution. However, experimental assessment of PHA biodegradation is challenged by its time- and resource-intensiveness. In this study, a comprehensive computational Quantitative Structure–Activity Relationship (QSAR)-based approach was developed to predict biodegradability of short chain length (scl)-PHA-based formulations consisting of various additives and building blocks. A novel curated dataset for the (scl)-PHA poly(-3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV), with literature-reported environmental and biodegradation parameters from lab-scale experiments in soil, marine, freshwater and compost systems, was constructed and used to develop and validate the introduced approach. Random forest (RF) and Extreme Gradient Boosting (XGBoost) machine learning (ML) models were optimized and validated with cross-validation and test set predictions. The optimal models reported high accuracy values of the coefficient of determination R², indicating excellent relationships between structure and biodegradation metrics. Further analysis of descriptor variable importance confirmed that biopolymer biodegradability was favorably affected by biodegradation time, while mechanisms, environmental conditions, and additives contributed secondary yet physically consistent effects. The proposed QSAR framework demonstrated a robust and interpretable web-based tool for predicting the environmental fate of PHBV in natural environments and supported the sustainable safe-by-design (SSbD) approach of next-generation biodegradable polymers. Full article

Recently, polyhydroxyalkanoates (PHAs) have gained significant attention as a bioactive material for replacing petrochemical plastics. PHAs can be produced by microorganisms growing on sludge substrates. In this study, fish-processing wastewater was investigated as an alternative substrate for PHA production using Bacillus cereus. Wastewater dilution, carbon-to-nitrogen ratio modification, and the addition of fish oil as a lipidic substrate were examined, and bacterial growth and biopolymer production were optimized. First, wastewater was diluted (25–100%) and examined. The 50% dilution treatment was selected, yielding a CDM of 0.426 g/L and a PHA content of 6.69%. In subsequent steps, the effects of wastewater fermentation and bacterial adaptation prior to the main production processes were investigated. According to the results, the 50% and 100% fermented treatments exhibited higher CDM values (0.970–1.022 g/L) compared to the non-fermented treatments. Cultures inoculated with adapted bacteria showed superior performance (CDM: 1.455 g/L, PHA: 0.499 g/L, PHA content: 34.63%) relative to non-adapted treatments. The effect of the carbon-to-nitrogen (C/N) ratio was also optimized by supplementing two carbon sources: glucose and crude fish oil. The optimal treatment T1 (effluent + 0.6 g/L glucose) had a CDM of 1.32 g/L and a PHA content of 0.215 g/L. Treatment 1, which consisted solely of effluent and fish oil, exhibited higher values (CDM: 1.12 g/L, PHA: 0.65 g/L) and was therefore considered the cost-effective treatment. Subsequently, a scale-up process was conducted in a 4 L bioreactor over 300 h under semi-continuous, long-term cultivation. The optimal harvesting time for the biopolymer was achieved during the fourth cycle (180–240 h). The produced biopolymer was characterized using FTIR, NMR, TGA, DSC, SEM, and XRD analyses, confirming the production of a copolymer, specifically poly(3-hydroxybutyrate-co-3-hydroxyvalerate). This study used wastewater from the fish industry for the production of biodegradable polyhydroxyalkanoates. Full article

Plastic manufacturing depends heavily on petroleum-derived monomers like terephthalic acid, the main component of polyethylene terephthalate (PET). However, the depletion of fossil resources and increasing environmental concerns have heightened the need for sustainable alternatives. Lignocellulosic biomass has emerged as a promising resource due to its renewable, abundant, and eco-friendly nature. Understanding its chemical composition enables conversion of this biomass into platform chemicals, such as 2,5-furandicarboxylic acid (FDCA) and lactic acid, derived from cellulose and hemicellulose. These can be polymerized into bio-based plastics such as polyethylene furanoate (PEF), polylactic acid (PLA), and polyhydroxyalkanoates (PHAs), offering greener alternatives to fossil-based plastics. PEF features rigid furan rings that enhance thermal stability, mechanical strength, and barrier properties, and reduce gas permeability compared to PET. PLA is a renewable, biodegradable plastic widely used in packaging and medical applications. This review covers the chemical composition of lignocellulosic biomass cellulose, hemicellulose, and lignin, and various pretreatment strategies, chemical, physicochemical, and physical, to overcome biomass recalcitrance and improve conversion efficiency. It also highlights recent catalytic advances in transforming cellulosic carbohydrates into bio-based plastic precursors such as FDCA and lactic acid. Lastly, this review discusses polymerization pathways for producing PEF and PLA, emphasizing their role in reducing the environmental impact of polymer manufacturing and promoting green chemistry principles. Full article

The challenge of substituting bone defects necessitates the search for effective biomaterials based on biopolymer composites with biocompatible fillers. A promising approach in bone tissue engineering is the use of regenerative scaffolds based on polyhydroxyalkanoates (PHAs), specifically poly(3-hydroxybutyrate)—P(3HB), which are characterized by high biocompatibility and osteoinductive potential. In this study, we evaluate the changes in the mechanical, thermal, and morphological properties of P(3HB) within P(3HB)-copolymers/HA, P(3HB)/CS, P(3HB)/PLA/CS, and P(3HB)/PLA/HA composites. These materials, containing various filler contents (up to 70 wt.% of HA–hydroxyapatite or CS–chitosan), were obtained using melt extrusion compounding. It is shown that the modification of biopolymer matrices promotes a decrease in melting temperature, improvement of mechanical characteristics, and an increase in material elasticity. At high filler concentrations, nanoparticle agglomeration and a deterioration of physical-mechanical properties were observed. It was established that a content of 10–20 wt.% of nano-hydroxyapatite and chitosan is optimal, as these composites most closely match the mechanical properties of bone tissue. The results obtained indicate the high potential of the developed nanocomposites for the creation of biodegradable implants in reconstructive orthopedics. Full article

Polyhydroxyalkanoates (PHAs) emerge as promising biodegradable polymers for sustainable applications, yet predicting their biodegradation behavior under different environmental conditions remains challenging. In this study, we propose a novel data-driven computational framework for predicting biodegradation-induced weight/mass loss in PHA-based materials. A comprehensive database of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV)-based formulations was manually curated by systematically collecting and harmonizing material descriptors, environmental parameters, and experimental biodegradation outcomes from laboratory- and large-scale studies conducted in soil, marine, freshwater, and compost environments. Multiple regression-based quantitative structure–activity relationship (QSAR) models were developed and rigorously validated, demonstrating high predictive performance and strong correlations between polymer structure, environmental conditions and degradation behavior. “Exposure time”, “degradation environment” and “hydroxybutyrate (HB) ratio” were identified as the most important features for weight loss. Finally, the predictive model was integrated into the Jaqpot computational platform, enabling open access and facilitating data-driven assessment and design of biodegradable polymer systems. Full article

Polyhydroxyalkanoates (PHAs) are biodegradable microbial polyesters that represent a promising sustainable alternative to petroleum-based plastics. Salterns, hypersaline environments, are recognized as significant sources of halotolerant microorganisms that can produce PHAs in high-salinity conditions; however, Vietnamese saltern ecosystems have not been extensively investigated. This research aimed to isolate and initially characterize salt-tolerant bacteria capable of synthesizing PHAs from the Hon Khoi saltern in Khanh Hoa Province, Vietnam. A total of 37 halotolerant bacterial isolates were obtained, and potential PHA-producing strains were initially screened using Sudan Black B and Nile Blue A. TEM microscopy was then employed to confirm the existence of PHA granules. Furthermore, FTIR spectroscopy and GC–MS/MS spectrometry were utilized to analyze the chemical structure and monomer composition of the extracted polymers. Six isolates were identified as PHA-producing bacteria, including Salinivibrio sp. HK101 and HK116, Halomonas sp. HK105, Priestia sp. HK125 and HK142, and Bacillus sp. HK130. These strains exhibited growth across 3–10% NaCl and temperatures from 25 to 45 °C. Priestia sp. HK142 and Salinivibrio sp. HK101 exhibited the most substantial PHA accumulation, achieving 50.72 ± 1.83% and 42.07 ± 1.8% of DCW, respectively. These results indicate that the Hon Khoi saltern represents a promising source of halotolerant PHA-producing bacteria with potential relevance for future biopolymer production studies. Full article

The large-scale production of microbial bioplastics remains limited by high production costs, reliance on refined substrates, and inefficient utilization of agro-industrial residues. Although sugarcane bagasse has been explored as a carbon source for polyhydroxyalkanoate production, studies have predominantly focused on poly (3-hydroxybutyrate) (PHB), with limited reports on copolymer synthesis from pentose-rich lignocellulosic streams. In this study, a newly isolated Bacillus sp. HLI02 was employed for the biosynthesis of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV), using pentosan-rich sugarcane bagasse hydrolysate as an inexpensive and sustainable carbon source. Fermentation parameters were systematically optimized at different pH and temperature, and the strain demonstrated efficient conversion of xylose-rich hydrolysate into PHBV without the requirement for external nutrient supplementation. Under optimized conditions (pH 7.0, 37 °C, and C/N ratio of 40), a maximum PHBV yield of 2 g/L, corresponding to 59.5% of cell dry weight, was achieved. Structural and compositional analyses using Fourier transform infrared spectroscopy (FTIR), gel permeation chromatography (GPC), and ¹H and ¹³C nuclear magnetic resonance (NMR) spectroscopy confirmed successful PHBV copolymer formation with well-defined structural characteristics. Thermal analysis revealed a decomposition temperature of 166 °C, indicating good thermal stability. The produced PHBV further exhibited favourable biocompatibility and biodegradability, supporting its potential applicability in sustainable packaging and related sectors. This work demonstrates the effective conversion of hemicellulosic sugarcane bagasse hydrolysate into PHBV using a newly isolated Bacillus strain, highlighting an underexplored route for copolymer production from agro-waste–derived C5 sugars. By integrating low-cost feedstock utilization with process optimization and comprehensive polymer characterization, this study contributes to the development of economically viable and sustainable bio-based polymer production strategies. Full article

Macroalgae represent a promising third-generation feedstock for biorefinery due to their high biomass productivity and non-reliance on arable land. However, their complex cell wall structure poses a significant barrier to efficient bioconversion. This review integrates current pretreatment methods, including physical, chemical, biological, and combined approaches, with a focus on their mechanisms, effectiveness, and limitations. Furthermore, it explores the conversion of pretreated macroalgal biomass into bioenergy and biochemicals, such as bioethanol, organic acid and polyhydroxyalkanoate, via microbial fermentation. The review also examines the application of genetic editing tools (e.g., CRISPR-Cas systems) for the targeted modification of macroalgae to improve their inherent characteristics for biorefinery, such as reducing biomass recalcitrance or increasing the content of target carbohydrates. Finally, future perspectives on technological innovations and integrated industrial chains of macroalgal biorefinery are discussed. This review serves as a systematic reference for deepening the understanding of macroalgal cell wall deconstruction processes and supports the development of efficient and environmentally benign pretreatment strategies to advance macroalgal biorefinery toward industrialization. Full article

Photodynamic therapy (PDT) is a promising localized strategy for the treatment of cervical cancer, ranking as the fourth most common cancer among women worldwide. The integration of photosensitizers (PSs) in localized drug delivery systems (DDSs), particularly in electrospun nanofibers, holds tremendous potential to overcome the drawbacks of their systemic administration. Exploring multilayer fibrous architectures provides a versatile therapeutic platform to design the next generation of localized DDS. In this work, localized implants for cancer treatment using PDT were developed using polyhydroxyalkanoate (PHA), chitosan (CS) and polyethylene oxide (PEO) as biopolymers and a porphyrin (Por) as PS, following two approaches: blended PHA/Por electrospun microfibers and multilayered membranes (PHA–Por/CS/PEO) produced by sequential electrospinning. The synthesized Por displayed higher cytotoxicity in light compared to dark against tumor cells. All the developed membranes were characterized regarding their morphology, wettability, absorption and fluorescence properties. PHA–Por membranes exhibited overall uniform fibrous morphologies with successful Por incorporation. Nonetheless, they presented a highly hydrophobic surface, compromising the Por release and cell–material interactions. In contrast, multilayer PHA–Por/CS/PEO membranes demonstrated enhanced hydrophilicity and enabled sustained Por release. Upon light irradiation, these membranes induced a significantly greater inhibition of HeLa cell proliferation (29.61%) compared to dark conditions (6.21%), confirming their photodynamic activity. Full article