RESUMO
The present study optimized pre-treatment conditions for bioenzyme-mediated hydro-distillation (BMHD) for extraction of mint oil from mentha leaves and the results were compared with those of traditional hydro-distillation (HD) method using response surface methodology. The bio-enzymes produced from moringa leaves had maximum pectinase activity (287.04 µg of sugar/min/ml) followed by xylanase (87.78 µg of sugar/min/ml) while endoglucanase, exoglucanase and amylase activities were comparatively low. The optimized conditions for HD were 69.08 temperature for 173.70 min with water:sample of 10.0. The optimized conditions for enzyme pre-treatment of mentha leaves by BMHD were enzyme concentration of 8%, for a period of 120 min at an incubation period of 40 â. The yield (%) and menthol content (%) of the oil at optimized conditions by HD were 1.55 ml/100 g of sample and 56.40% menthol content, respectively, and for BMHD the yield and menthol content (%) of the oil at optimized conditions were 3.69% and 72.80%, respectively. It was found that BMHD leads to a 130% increase in the yield of mint oil and a 10% increase in menthol content as compared to the HD method. No significant difference in physical parameters was observed in mint oil extracted via both methods. Therefore, BMHD is a cost-effective and sustainable approach having an edge over the HD method without compromising the quality and could be a viable approach for commercial purposes.
Assuntos
Destilação , Mentha , Mentol , Folhas de Planta , Mentha/química , Mentol/química , Folhas de Planta/química , Destilação/métodos , Óleos de Plantas/químicaRESUMO
The cooperative role of vital components of the antioxidative defense pathway in addition to redox couples was studied in a growth-phase dependent manner at 20, 30, and 40 days after subculturing (DAS) in five different euryhaline microalgal strains (EMS) Scenedesmus MKB (B-S), Spirulina subsalsa (B-6), Anabaena sp. (B-7), Chlorella sp. (B-8), and Chlorosarcinopsis eremi (B-18) collected from waterlogged areas of Punjab, India and in two freshwater microalgal strains (FMS). EMS surpasses to maintain a high redox couple's ratio ascorbic acid/dehydroascorbate (AsA/DHA), and reduced glutathione/oxidized glutathione (GSH/GSSG) through a close-knit pattern of antioxidative enzymes including high specific activities of ascorbate peroxidase (APX), monodehydroascorbate reductase (MDHAR), glutathione reductase (GR), dehydroascorbate reductase (DHAR) and less specific activity of glutathione peroxidase (GPX). While FMS struggled for the same irrespective of near similar total glutathione and higher specific activity of GPX might be answerable for the lesser redox ratio than EMS. However, high specific activity of catalase (CAT) might be sought to compensate for the less increase of APX in FMS. The fact significantly less H2O2, and malondialdehyde (MDA) with DAS in EMS than in FMS and higher redox ratios exquisitely elevate their tolerance ability making EMS a captivating prospect for cultivation in waterlogged areas. Additionally, their abundance of potent antioxidants further highlights the potential of EMS as an excellent source of these beneficial compounds.
RESUMO
Microalgae have gained recognition due to the occurrence of nutraceuticals which are sustainable reservoir to substitute the organic chemical-based health supplements. The biomass of microalgae incorporates various functional biomolecules like chlorophyll, carotenoids and phenols that exhibit therapeutic properties and act as nutraceuticals. In spite of the higher production of the microalgal biomass, difference in their biochemical composition, and lack of characterization for nutraceutical properties are the prime hindrance in upscaling these bio-factories. Two euryhaline microalgal strains viz. BGLR8 and BGLR16, isolated from water-logged areas of Punjab, India were screened for biomass production and characterized for the nutraceutical properties using biochemical estimations. Results of the study indicated that BGLR8 retained maximum amount of lipids (86 mg/g), total chlorophyll (29.42 mg/g), carotenoids (28.82 mg/g), phenols (4.46 mg/g), phycocyanin (52 mg/g), astaxanthin (19.27 mg/g) and ß-carotene (5.6 mg/g) and anti-oxidant activity (31.73%) as compared to BGLR 16. The results of gas chromatography-mass spectrometry (GC-MS) study revealed the presence of 8 therapeutic compounds like Dimethyl (E)-but-2-enedioate, Hexasilacyclododecane, Heptasilacyclotetradecane, Methyl (Z)-pentadec-8-enoate, Methyl octadec-13-enoate, Methyl hexadecanoate, Methyl octadecanoate, Methyl-octadeca-9,12-dienoate in BGLR8. Molecular identification through 18S rRNA gene sequencing confirmed BGLR8 to be a member of genus Coelastrella. (GenBank accession no. MW443083.1). Microalgae can be used as an alternate and feasible source of PUFAs; however, only a few species are employed for PUFA synthesis, necessitating additional in-depth research and the isolation of novel strains.
Assuntos
Microalgas , Biomassa , Carotenoides , Clorofila , Ácidos Graxos Insaturados , Microalgas/genética , FenóisRESUMO
The present study reports the pretreatment of paddy straw by Trichoderma reesei MTCC 164 and Coriolus versicolor MTCC 138 to observe the changes in chemical composition and its correlation with change of surface structure, morphology and porosity of paddy straw. Compared with untreated straw, cellulose decreased by 15.9 and 19.3 % in T. reesei MTCC 164 and C. versicolor MTCC 138 pretreated paddy straw respectively. Lignin content increased by 41.4 % in T. reesei pretreated paddy straw whereas decreased by 19.1 % in C. versicolor pretreated straw. The microscopic structural changes were examined by scanning electron microscopy under reasonable conditions. Results showed that digestibility of paddy straw are increased by treating paddy straw with both the cultures. Both surface area and pore size of treated straw were increased partially due to solubilization of silica components.
RESUMO
This study investigated the effect of enzymatic and hydrothermal pretreatment approaches on the solubilization of organic matter, structure, and biogas yield from microalgal biomass. The soluble chemical oxygen demand (sCOD) concentration increased by 1.21-3.30- and 5.54-6.60-fold compared to control by enzymatic and hydrothermal pretreatments respectively. The hydrothermal pretreatment affected the structural changes in the microalgal biomass markedly; nonetheless, increased enzymatic concentration also had a definite effect on it as determined by qualitative approaches like scanning electron microscopy and Fourier transform infrared spectroscopy. Also, the hydrothermal pretreatment (100 °C for 30 min) resulted in the highest biogas production potential (P) of 765.37 mLg-1 VS at a maximum biogas production rate (Rm) of 22.66 mLg-1 day-1 with a very short lag phase (λ) of 0.07 days. The biogas production of pretreated microalgal biomass particularly at higher enzyme dose (20%, 24 h) and higher hydrothermal pretreatment temperature (120 °C, 30 min) showed a significant but weak correlation (R = 0.53) with sCOD, thus demonstrating that the less organic matter was used up for the biogas production. The modified Gompertz model explained the anaerobic digestion of microalgal biomass more accurately and had a better fit to the experimental data comparatively because of the low root mean square error (3.259-16.728), residual sum of squares (78.887-177.025), and Akaike's Information Criterion (38.605-62.853).
Assuntos
Clorofíceas , Microalgas , Biocombustíveis , Biomassa , Anaerobiose , MetanoRESUMO
The most cost-effective technique to cultivate microalgae is with low-cost resources, like fruit and vegetable peels. This study examined the viability of culturing microalgae (Oscillatoria sancta PCC 7515) isolated from a waterlogged region of Punjab, India, in a low-cost medium (fruit and vegetable waste peels) for pharmaceutical use. 16S rRNA sequencing discovered O. sancta PCC 7515. Fruit and vegetable peels were mineralized and chemically analyzed. At a 5% Bacillus flexus concentration, fruit and vegetable peels were liquefied at room temperature for 24 h. Response Surface Methodology (RSM) was used to assess and improve important cultural variables. The RSM predicted the best results at 10 pH, 30 days of incubation, 5% inoculum concentration, and 5% fruit and vegetable waste liquid leachate. The optimum conditions yielded more biomass than the basal conditions (0.8001 g/L). O. sancta PCC 7515 produced more lipids, proteins, Chl a, and Chl b in a formulated alternate medium than standard media. This study shows that O. sancta PCC 7515 may thrive on fruit and vegetable peel media. Fruit and vegetable waste (FVW) media assure low-cost microalgae-based functional foods.
RESUMO
The microalga was isolated from Muktsar, the southwestern zone of Indian Punjab and identified as Asterarcys quadricellulare BGLR5 (MF661929) by 18S rRNA sequence analysis. The optimization of various cultural factors by the Plackett-Burman and central composite (CCD) designs helped in discerning the significant cultural factors for the increased production of biomass and other functional components (chlorophyll, carbohydrate, lipid and protein). The optimal cultural conditions as per the model were pH 9.9, 81 µmol m-2 s-1 light intensity, 22 °C temperature, growth period of 25 days, NaNO3 12 mM, 15 mM NH4Cl, and 7 mM K2HPO4. In comparison to the basal condition biomass (0.886 g L-1), a 0.42-fold increase in biomass yield was attained. Further, the highest yield of biogas (P: 361.81 mL g-1 VS) with enhanced biogas production rate (R m: 8.19 mL g-1 day-1) was achieved in co-digesting paddy straw with Asterarcys quadricellulare biomass in 1:1 ratio compared to their digestion individually. Further, the co-digestion resulted in the positive synergistic effect which increased the observed biogas yield compared to the estimated yield by 11-58% depending upon the amount of algal biomass and paddy straw used. Hence, the present study signifies that the biomass of Asterarcys quadricellulare BGLR5 can be utilized as a co-substrate with paddy straw to enhance the biogas yield. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s13205-021-02792-x.