Polyherbal decoction modulates redox homeostasis during Malachite green induced metabolic stress in Saccharomyces cerevisiae

17-26Malachite green (MG) is aquatic pollutant that induces oxidative stress when comes in contact with the living organisms. In Saccharomyces cerevisiae, MG produces intracellular reactive oxygen species (ROS) and these ROS disturb redox homeostasis and cellular functions leading to early cell death. Exogenous supply of natural antioxidants containing polyherbal decoction may play a crucial role in re-establishment of redox homeostasis by ensuring the cell survival. Exposure of MG to Saccharomyces cerevisiae resulted in a significant decrease (97.8%) in colony forming units (CFU). An Ayurvedic polyherbal formulation ‘Vayasthapana Rasayana’ (VR) which contains natural antioxidants from plants viz. Terminalia chebula, Clitoria ternatea, Boerhaavia diffusa, Centella asiatica, Phyllanthus emblica, Asparagus racemossus and Tinospora cordifolia at 1.0 mg/mL concentration could arrest the oxidative stress during MG exposure. Levels of ROS elevated up to 67.3% on MG exposure; while VR supplementation reduced it by 54.7%. MG induced cellular apoptosis in 38% and necrosis in 27% cells, while VR augmentation reduced it to 8%. Activities of antioxidant enzymes like catalase, superoxide dismutase and glutathione peroxidase in MG exposed cells were induced by 408, 144 and 140%, respectively, whereas, VR supplementation lowered the expressions to 102, 57 and 111%, respectively. Induction in caspases 3/7 activity was also found to be reduced by 65.39% after VR augmentation. Similarly, VR modulated activities of oxido-reductases like lignin peroxidase, laccase, NADH-DCIP reductase and MG reductase. VR supplementation also maintained the MG utilization potential of S. cerevisiae up to 20th exposure cycle which was otherwise arrested to 8th cycle. The treatment also decreased the ROS accumulation and nuclear damage, restoring the cell viability up to 94% and retained normal growth dynamics. Thus, VR supplementation could significantly decrease oxidative stress, enhance cell viability and ultimately protect the dying S. cerevisiae cells during MG exposure

Polyherbal decoction modulates redox homeostasis during Malachite green induced metabolic stress in Saccharomyces cerevisiae

Malachite green (MG) is aquatic pollutant that induces oxidative stress when comes in contact with the living organisms. In Saccharomyces cerevisiae, MG produces intracellular reactive oxygen species (ROS) and these ROS disturb redox homeostasis and cellular functions leading to early cell death. Exogenous supply of natural antioxidants containing polyherbal decoction may play a crucial role in re-establishment of redox homeostasis by ensuring the cell survival. Exposure of MG to Saccharomyces cerevisiae resulted in a significant decrease (97.8%) in colony forming units (CFU). An Ayurvedic polyherbal formulation ‘Vayasthapana Rasayana’ (VR) which contains natural antioxidants from plants viz. Terminalia chebula, Clitoria ternatea, Boerhaavia diffusa, Centella asiatica, Phyllanthus emblica, Asparagus racemossus and Tinospora cordifolia at 1.0 mg/mL concentration could arrest the oxidative stress during MG exposure. Levels of ROS elevated up to 67.3% on MG exposure; while VR supplementation reduced it by 54.7%. MG induced cellular apoptosis in 38% and necrosis in 27% cells, while VR augmentation reduced it to 8%. Activities of antioxidant enzymes like catalase, superoxide dismutase and glutathione peroxidase in MG exposed cells were induced by 408, 144 and 140%, respectively, whereas, VR supplementation lowered the expressions to 102, 57 and 111%, respectively. Induction in caspases 3/7 activity was also found to be reduced by 65.39% after VR augmentation. Similarly, VR modulated activities of oxido-reductases like lignin peroxidase, laccase, NADH-DCIP reductase and MG reductase. VR supplementation also maintained the MG utilization potential of S. cerevisiae up to 20th exposure cycle which was otherwise arrested to 8th cycle. The treatment also decreased the ROS accumulation and nuclear damage, restoring the cell viability up to 94% and retained normal growth dynamics. Thus, VR supplementation could significantly decrease oxidative stress, enhance cell viability and ultimately protect the dying S. cerevisiae cells during MG exposure

Enzymatic hydrolysis of biologically pretreated sorghum husk for bioethanol production

Biological pretreatment of lignocellulosic biomass is considered to be energy-efficient and cost-effective. In the present study, sorghum husk was biologically pretreated with a white-rot fungus Phanerochaete chrysosporium (MTCC 4955) under submerged static condition. Ligninolytic enzymes like lignin peroxidase (0.843 U/mL) and manganese peroxidase (0.389 U/mL) played an important role in the biological pretreatment of sorghum husk. Activities of different hydrolytic enzymes such as endoglucanase (57.25 U/mL), exoglucanase (4.76 U/mL), filter paperase (0.580 U/mL), glucoamylase (153.38 U/mL), and xylanase (88.14 U/mL) during biological pretreatment of sorghum husk by P. chrysosporium were evaluated. Enzymatic hydrolysis of untreated sorghum husk and biologically pretreated sorghum husk produced 20.07 and 103.0 mg/g reducing sugars, respectively. This result showed a significant increase in reducing sugar production in the biologically pretreated sorghum husk as compared to its untreated counterpart. Biologically pretreated sorghum husk hydrolysate was further fermented for 48 h using Saccharomyces cerevisiae (KCTC 7296), Pachysolen tannophilus (MTCC 1077), and their co-culture resulting in ethanol yields of 2.113, 1.095, and 2.348%, respectively. The surface characteristics of the substrate were evaluated after the delignification and hydrolysis, using FTIR, XRD, and SEM, confirming the effectiveness of the biological pretreatment process

Effect of methomyl on hepatic mixed function oxidases in rats

Objective: To study the effect of the methomyl on mixed function oxidase system in rats. Materials and Methods: The effect of the methomyl on mixed function oxidase was studied using different dosages, durations and sex. Microsomes were isolated using the calcium precipitation method. The levels of cytochrome P 450 , and cytochrome b 5 were determined using extinction coefficient of 91 and 85 mM -1 respectively. The activities of drug metabolizing enzymes, hemoglobin content, liver function enzymes, and serum cholinesterase activity were assayed by using standard methods. Results: Intraperitoneal administration of methomyl (4 mg/kg body weight) showed significant decrease in the level of cytochrome P 450 , and the activities of aminopyrine N-demethylase and aniline hydroxylase on the third day of the treatment. Methomyl (4 mg/kg) treatment of old male rat and adult female rat also showed a decrease in the level of cytochrome P 450 , and aminopyrine N-demethylase activity. The serum samples from methomyl treated rats (male and female), when analyzed for alanine aminotransferase (SGPT) and aspartate aminotransferase (SGOT) as markers of the liver toxicity, showed significant increase in the activity. The activities of SGPT and SGOT were significantly higher in the treated rats (2 and 4 mg/kg) than in the control group. A significant decrease in the level of hemoglobin and serum cholinesterase activity was observed, when there was an increase in the dose level. A significant increase was observed in alkaline phosphatase activity at all dose levels. Conclusion: Methomyl influences mixed function oxidase and creates abnormality of liver functions in the rats. This effect depends on the dose and duration of methomyl

Conserved nature of Helicoverpa armigera gut bacterial flora on different host plants and in vitro interactions with PI proteins advocates role in host digestive physiology

Helicoverpa armigera is anxious insect pest of agricultural crops. Array of defensive molecules in host plants and extensive use of chemical insecticides are unable to cease the attack incidences. Gut bacterial communities are found to contribute in various physiological activities in most of the arthropods. In the current study the bacterial communities were isolated from gut of H. armigera feeding on three host plants (Pigeonpea, Chickpea and Cotton) by culture dependent and culture independent methods. Predominant bacterial communities were identified by terminal restriction fragment length polymorphism (TRFLP). Three dominant phylotypes namely proteobacteria, actinobacteria and firmicutes were identified by TRFLP and found to conserve on different host plant selected. Five Bacillus species namely Bacillus sp. JR14, Bacillus sp. YP1, Bacillus safensis CG1, Bacillus subtillis KAVK2 and Bacillus megaterium 47N were purified by culture dependent method and identified by 16S rRNA sequencing. Among all identified Bacillus, Bacillus sp. YP1 strain was found to be potent protease producer as assisted by dot-blot assay and in vitro solution assays. The in vitro interactions of these proteases with host plant PIs were studied by reverse zymography and gel X-ray contact print (GXCP) analysis. Reduction in activity of PIs and degradation pattern of PI bands on gels in presence of trypsin and protease extract of Bacillus sp. YP1 indicates inactivation of PIs. Thus, conserved nature and in vitro response to PI proteins advocates role of gut bacterial flora in H. armigera digestive physiology. Keywords: H. armigera, Gut bacterial proteases, Host plant defense, PIs, TRFL

Phytoextracts protect <i>Saccharomyces cerevisiae</i> from oxidative stress with simultaneous enhancement in bioremediation efficacy

469-478Bioremediation efficacies are highly affected by abiotic stresses imparted by a verity of pollutants due to generation of reactive oxygen species (ROS). These stressed cells can be treated using natural or synthetic antioxidants. Such an approach could prove beneficial to bioremediation agents as the exogenously added antioxidant compounds would scavenge the generated free radicals. This would definitely lead to increased longevity of the involved organism and carry out superior treatments. In present study, Malachite Green (MG) was found to exert oxidative stress on Saccharomyces cerevisiae through generation ROS. A 2 h exposure of MG though achieved 99% decolourization, the cells revealed a significant decrease (97.8%) in colony forming units (CFU) upon further subculture. Natural antioxidants from Centella asiatica, Phyllanthus emblica, Asperagus racemosus and Tinospora cordifolia extracts, however, restored the CFU with a loss of only 16-33%. The MG stressed cells indicated an increase in ROS by 6.7 fold which was reduced to near normal due to augmentation with plant extracts. MG damaged the nuclear material up to 90% and inclusion of phytoextracts protected the cells revealing only 0-7% nuclear damage. Induction in apoptosis (92%) and necrosis (23%) in MG exposed cells was noted, while plant extracts augmentation reduced apoptosis to 15-49% and necrosis to 10-16%. Activities of antioxidant enzymes such as superoxide dismutase, catalase and glutathione peroxidase were significantly decreased in phyto-augmented cells when compared to MG stressed cells. Dye degrading enzymes, namely lignin peroxidase, laccase, NADH-DCIP reductase and MG reductase were found to show induction in activities during MG utilization. Since antioxidants from plant extracts could protect the cells form oxidative stress, they were used to treat MG for 20 continuous decolourization cycles. Augmentation of C. asiatica, P. emblica, A. racemosus and T. cordifolia extracts at 20th decolourization cycle revealed 75, 79, 74 and 93% superior decolorization efficacies as compared to unaugmented cells. These natural antioxidants to protect bioremediation agents form oxidative stress, thus concluded to show enhanced treatment

New molecular phylogenetic evidence for Indian endemic species of the tribe Merremieae, Convolvulaceae

Recent advances in molecular phylogenetics in the family Convolvulaceae Juss., (particularly in formerly recognized tribe Merremieae) have brought new insights on generic delimitation. Therefore, many species were transferred across genera to accommodate in the new classification. However, additional morphological and molecular analyses are still needed to address the affinities and position of some species formerly included in Merremia Dennst. ex Endl.s.l. and allied genera. In this study, we provide a phylogenetic framework for the placement of Indian species in a new generic arrangement and to address the status of doubtful distinct species. Distimake rhyncorhiza (Dalzell) A.R.Simões & Staples is proved to have its place in Distimake Raf., while Operculina tansaensis Santapau & Patel is validated as a distinct species from O. turpethum (L.) Silva Manso. A nomenclatural clarification for the misuse of the name “Merremia gangetica (L.) Cufod.” in India is provided, with an encouragement to use the correct name Merremia emarginata (Burm.f.) Hallier f. The addition of the Indian species to the molecular phylogeny suggests the possible non-monophyly of Camonea Raf., and a new placement for Camonea vitifolia (Burm.f.) A.R.Simões & Staples, albeit still weakly supported. We have provided morphological descriptions, distribution maps and notes on nomenclature

Exploiting the efficacy of <i>Lysinibacillus</i> sp. RGS for decolorization and detoxification of industrial dyes, textile effluent and bioreactor studies

<div><p>Complete decolorization and detoxification of Reactive Orange 4 within 5 h (pH 6.6, at 30°C) by isolated <i>Lysinibacillus</i> sp. RGS was observed. Significant reduction in TOC (93%) and COD (90%) was indicative of conversion of complex dye into simple products, which were identified as naphthalene moieties by various analytical techniques (HPLC, FTIR, and GC–MS). Supplementation of agricultural waste extract considered as better option to make the process cost effective. Oxido-reductive enzymes were found to be involved in the degradation mechanism. Finally <i>Loofa</i> immobilized <i>Lysinibacillus</i> sp. cells in a fixed-bed bioreactor showed significant decolorization with reduction in TOC (51 and 64%) and COD (54 and 66%) for synthetic and textile effluent at 30 and 35 mL h⁻¹ feeding rate, respectively. The degraded metabolites showed non-toxic nature revealed by phytotoxicity and photosynthetic pigments content study for <i>Sorghum vulgare</i> and <i>Phaseolus mungo</i>. In addition nitrogen fixing and phosphate solubilizing microbes were less affected in treated wastewater and thus the treated effluent can be used for the irrigation purpose. This work could be useful for the development of efficient and ecofriendly technologies to reduce dye content in the wastewater to permissible levels at affordable cost.</p></div

Uptake and biodegradation of emerging contaminant sulfamethoxazole from aqueous phase using Ipomoea aquatica

Plants serve as appropriate markers of worldwide pollution because they are present in almost every corner of the globe and bioaccumulate xenobiotic chemicals from their environment. The potential of a semi-aquatic plant, Ipomoea aquatica, to uptake and metabolize sulfamethoxazole (SMX) was investigated in this study. I. aquatica exhibited 100% removal of 0.05 mg L ???1 SMX from synthetic media within 30 h. The I. aquatica achieved 93, 77 and 72% removal of SMX at 0.2, 0.5 and 1 mg L ???1 , respectively, after 48 h. This indicated that removal efficiency of I. aquatica was deteriorating at high concentrations of SMX. The chlorophyll and carotenoid content of I. aquatica was insignificantly influenced by SMX irrespective of its high concentration. Similarly, scanning electron microscopy (SEM) showed that exposure to SMX had an insignificant impact on morphology of the plant organelles. The mechanisms of removal by I. aquatica were explored by evaluating contributions of bioadsorption, bioaccumulation and biodegradation. There was negligible adsorption of SMX to plant roots. Accumulation of SMX within plant roots and stems was not observed; however, I. aquatica accumulated 17% of SMX in leaves. Thus, the major mechanism of elimination of SMX was biodegradation, which accounted for 82% removal of SMX. Gas chromatography-mass spectrometry (GC-MS) confirmed that I. aquatica biodegraded SMX into simpler compounds, and generated 4-aminophenol as its final product. A laboratory scale phytoreactor was used to investigate the application of I. aquatica in a simulated system, where it achieved 49% removal of SMX (0.2 mg L ???1 ) in 10 d. ?? 2019 Elsevier Lt