Maximum Cell Growth Research Articles

Isolation, identification, and characterization of Bacillus subtilis SMP-2 from panitenga and exploring its potential for biosurfactant production

A traditional Assamese fermented food, Panitenga, was explored for potential probiotic isolation. A potent bacterial strain exhibiting biosurfactant production ability was isolated, characterized, and identified as Bacillus subtilis SMP-2. Environmental parameters were optimized for maximum cell growth and biosurfactant production that was found to be pH 6, 30°C, 130 rpm, with glycerol as the carbon (C) source, yeast extract as the nitrogen (N) source, and a C/N ratio of 3:1. At these optimized conditions, the strain yielded 8.13 ± 0.9 g/L of lipopeptide biosurfactant. This biosurfactant remarkably reduced the surface tension of water from 72 mN/m to 37 ± 0.36 mN/m, possessed a low critical micelle concentration (CMC) of 125 mg/L, and exhibited antimicrobial properties. It persisted to be stable across a wide range of physical conditions, including variations in pH, temperature, and salinity. The significantly high production yield and noteworthy properties of the biosurfactant from Bacillus subtilis SMP-2 make it a promising candidate for applications in microbial-enhanced oil recovery (MEOR), bioremediation of oil spills, production of cosmetics and pharmaceuticals, contributing to economic growth and sustainable development.

Phytochemical Profiles and Cytotoxic Activity of Bursera fagaroides (Kunth) Engl. Leaves and Its Callus Culture.

Bursera fagaroides, popularly used in México, possesses bioactive lignans. These compounds are low in the bark, and its extraction endangers the life of the trees. The aim of the present investigation was to search for alternative sources of cytotoxic compounds in B. fagaroides prepared as leaves and in vitro callus cultures. The friable callus of B. fagaroides was established using a combination of plant growth regulators: 4 mgL-1 of 2,4-dichlorophenoxyacetic acid (2,4-D), 1 mgL-1 Naphthaleneacetic Acid (NAA) and 1 mgL-1 Zeatin. The maximum cell growth was at day 28 with a specific growth rate of μ = 0.059 days-1 and duplication time td = 11.8 days. HPLC quantification of the dichloromethane callus biomass extract showed that Scopoletin, with a concentration of 10.7 µg g-1 dry weight, was the main compound inducible as a phytoalexin by the addition of high concentrations of 2,4-D, as well as by the absence of nutrients in the culture medium. In this same extract, the compounds γ-sitosterol and stigmasterol were also identified by GC-MS analysis. Open column chromatography was used to separate and identify yatein, acetyl podophyllotoxin and 7',8'-dehydropodophyllotoxin in the leaves of the wild plant. Cytotoxic activity on four cancer cell lines was tested, with PC-3 prostate carcinoma (IC50 of 12.6 ± 4.6 µgmL-1) being the most sensitive to the wild-type plant extract and HeLa cervical carcinoma (IC50 of 72 ± 5 µgmL-1) being the most sensitive to the callus culture extract.

Development of a new sterilization method for microalgae media using calcium hypochlorite as the sterilant.

Calcium hypochlorite (Ca(ClO)2), which can be stably stored in powder form for a long period, is widely used as a disinfectant in various fields. A new sterilization process was developed in the present study, where a microalgal medium was sterilized using 0.02% Ca(ClO)2, followed by complete neutralization of the Ca(ClO)2 within 8h through catalytic reaction of an MnCl2-Na2EDTA complex and a synergistic effect of glucose. When comparing the growth of Chlorella vulgaris in the autoclaved medium, a 2.65 times greater maximum cell growth was observed in cells grown in the medium prepared by treatment of Ca(ClO)2. This result indicates that denaturation of the medium by heat can hinder the growth of some microorganisms. In the case of cultivation of Euglena gracilis, successful culture growth was achieved without growth inhibition or contamination on a medium prepared in the same manner.

Kinetics of microbial cell growth, utilization of organic substrates and methane production in upflow anaerobic filters in two and three separated stages treating sanitary landfill leachates

AbstractThis paper deals with the kinetics of microbial cell growth, utilization of organic substrates and methane production in upflow anaerobic filters in two and three separated stages (UAF‐2SS and UAF‐3SS) treating sanitary landfill leachates, under three temperatures (20, 27, and 34°C), fed with volumetric organic loads (VOLs) for UAF‐2SS (1.8, 2.25, 2.76, 3.45, 3.71, 4.64 kgCOD (chemical oxygen demand)/m3/d) and UAF‐3SS (1.7, 2.25, 2.44, 2.6, 3.15, 3.45, 3.5, 4.57, 4.64, 6.31, 11.61, 14.18, 17.48 kgCOD/m3/d). Kinetic parameters were obtained at temperature (20–34°C), pH (8.8–9.1), each one of three stages within the UAF‐2SS and UAF‐3SS reactors containing methanogenic bacteria (Methanococcus sp., and Methanobacterium sp.) and Clostridium sp.: Maximum substrate utilization rate (rm,s) resulted in 102 mg COD/L/h, maximum microbial cell growth rate (μm) varied 102–103 CFU (colony forming units)/mL/h, methane (CH4) production rate (rm,CH4) tended to vary 100–101 mg CH4/d and the maximum production coefficient (Y) varied 0–102 CFU/mL/h/mgCOD/L/h.

Dibutyl phthalate degradation by Paenarthrobacter ureafaciens PB10 through downstream product myristic acid and its bioremediation potential in contaminated soil

Dibutyl phthalate (DBP) is a widely used plasticizer to make plastic flexible and long-lasting. It is easily accessible in a broad spectrum of environments as a result of the rising level of plastic pollution. This compound is considered a top-priority toxicant and persistent organic pollutant by international environmental agencies for its endocrine disruptive and carcinogenic propensities. To mitigate the DBP in the soil, one DBP-degrading bacterial strain was isolated from a plastic-polluted landfill and identified as Paenarthrobacter ureafaciens PB10 by 16S rRNA gene sequence-based homology. The strain was found to develop a distinct transparent halo zone around grown colonies on an agar plate supplemented with DBP. The addition of yeast extract (100 mg/L) as a nutrient source accelerated cell biomass production and DBP degradation rate; however, the presence of glucose suppressed DBP degradation by the PB10 strain without affecting its ability to proliferate. The strain PB10 was efficient in eliminating DBP under various pH conditions (5.0–8.0). Maximum cell growth and degradation of 99.49% at 300 mg/L DBP were achieved in 72 h at the optimized mineral salt medium (MS) conditions of pH 7.0 and 32 °C. Despite that, when the concentration of DBP rose to 3000 mg/L, the DBP depletion rate was measured at 79.34% in 72 h. Some novel intermediate metabolites, like myristic acid, hexadecanoic acid, stearic acid, and the methyl derivative of 4-hydroxyphenyl acetate, along with monobutyl phthalate and phthalic acid, were detected in the downstream degradation process of DBP through GC-MS profiling. Furthermore, in synchronization with native soil microbes, this PB10 strain successfully removed a notable amount of DBP (up to 54.11%) from contaminated soil under microcosm study after 10 d. Thus, PB10 has effective DBP removal ability and is considered a potential candidate for bioremediation in DBP-contaminated sites.

CONTINUOUS PEDIOCIN PRODUCTION BY PEDIOCOCCUS ACIDILACTICI USING DAIRY WASTE

Objective: The production of pediocin by Pediococcus acidilactici has been conducted in continuous operation using dairy waste, namely whey. Methods: Whey supplemented with yeast extract was used as growth media of P. acidilactici. A series of batch fermentation have been conducted in whey with varying concentrations (0–40 g/L) of yeast extract. A continuous mode of fermentation was performed at the dilution rate of 0.05–0.25/h. The volumetric productivity of pediocin in continuous run has also been compared with batch process. A mathematical model has been developed to explain the reactor performance for pediocin production in both batch and continuous processes. Results: The highest specific pediocin production rate (36.8 AU mg/cell dry mass/h) and growth rate (0.41/h) were observed in batch runs using whey broth supplemented with 20 g/L yeast extract. Maximum cell growth and pediocin activity were obtained at 1.36 g/L and 2286 AU/mL in batch experiments. The highest pediocin productivity (514125 AU/h) was found in continuous mode for a dilution rate of 0.0625/h. The model was validated through well matching of simulated data with experimental ones. Conclusion: The study should be suitable for large-scale implementation of pediocin production.

Development and characterization of a new muscle cell culture system from Clarias magur (Hamilton, 1822).

The cell line has been used as a novel in vitro tool for executing several studies in life sciences. The current study aimed to develop and characterize a muscle cell culture system derived from Clarias magur. The primary muscle cell cultures derived from the caudal peduncle muscle have been successfully sub cultured up to 13 passages to establish a new muscle cell culture system known as CMM. At a temperature of 28°C, L-15 medium supplemented with 20% FBS produced the maximum growth of muscle cells. However, muscle cells were optimized to grow at 10% FBS. To enhance the proliferation capacity of the CMM cells, a growth-promoting factor bFGF (10ng/ml) was added, thereby reducing the time interval of passages for the subsequent cultures. DNA barcoding of the CMM cell culture system authenticated the species of origin. The cell culture system was successfully cryopreserved by a slow freezing procedure at - 80°C with a revival efficiency of 60%.

Tolperisone induces UPR-mediated tumor inhibition and synergizes with proteasome inhibitor and immunotherapy by targeting LSD1

ABSTRACT Background Drug repurposing is an attractive strategy for extending the arsenal of oncology therapies. Tolperisone is an old centrally acting muscle relaxant used for treatment of chronic pain conditions. In this study, we investigated the therapeutic effect and mechanism of tolperisone in human cancers and explored the combination strategy with proteasome inhibitor and immunotherapy. Research design and methods The antitumor effect of tolperisone was evaluated by measuring half maximal inhibitory concentration, cell death, and cell growth. RNA sequencing, western blotting, molecular docking, enzyme activity assay, and ChIP-qPCR were performed to reveal the underlying mechanism. Xenograft models were used to evaluate the efficacy of tolperisone alone or in combination with proteasome inhibitor or immunotherapy. Results Tolperisone inhibited cell growth and induced cell death in human cancer cell lines. Unfolded protein responses (UPR) pathway was hyperactivated in tolperisone-treated cells. We further identified histone lysine-specific demethylase 1 (LSD1) as a potential target of tolperisone, which directly demethylates UPR-related genes in H3K4me2. Tolperisone synergistically improved the efficacy of MG132 by enhancing UPR and sensitized tumors to immunotherapy by reprogramming M2 macrophages into M1 phenotype. Conclusions Tolperisone inhibits human cancer by targeting LSD1. Repurposing tolperisone in cancer therapy by a combination strategy implies clinical potential.

Cost-Effective Cultivation of Native PGPB Sinorhizobium Strains in a Homemade Bioreactor for Enhanced Plant Growth.

The implementation of bioreactor systems for the production of bacterial inoculants as biofertilizers has become very important in recent decades. However, it is essential to know the bacterial growth optimal conditions to optimize the production and efficiency of bioinoculants. The aim of this work was to identify the best nutriment and mixing conditions to improve the specific cell growth rates (µ) of two PGPB (plant growth-promoting bacteria) rhizobial strains at the bioreactor level. For this purpose, the strains Sinorhizobium mexicanum ITTG-R7T and Sinorhizobium chiapanecum ITTG-S70T were previously reactivated in a PY-Ca2+ (peptone casein, yeast extract, and calcium) culture medium. Afterward, a master cell bank (MCB) was made in order to maintain the viability and quality of the strains. The kinetic characterization of each bacterial strain was carried out in s shaken flask. Then, the effect of the carbon and nitrogen sources and mechanical agitation was evaluated through a factorial design and response surface methodology (RSM) for cell growth optimization, where µ was considered a response variable. The efficiency of biomass production was determined in a homemade bioreactor, taking into account the optimal conditions obtained during the experiment conducted at the shaken flask stage. In order to evaluate the biological quality of the product obtained in the bioreactor, the bacterial strains were inoculated in common bean (Phaseolus vulgaris var. Jamapa) plants under bioclimatic chamber conditions. The maximum cell growth rate in both PGPB strains was obtained using a Y-Ca2+ (yeast extract and calcium) medium and stirred at 200 and 300 rpm. Under these growth conditions, the Sinorhizobium strains exhibited a high nitrogen-fixing capacity, which had a significant (p < 0.05) impact on the growth of the test plants. The bioreactor system was found to be an efficient alternative for the large-scale production of PGPB rhizobial bacteria, which are intended for use as biofertilizers in agriculture.

Environmental factors affecting akinete germination and resting cell awakening of two cyanobacteria

Globally, cyanobacteria frequently cause blooms that outcompete other species in the waterbody, affecting the diversity, decreasing water exchange rates, and promoting eutrophication that leads to excessive algal growth. Here, Dolichospermum circinale (akinetes) and Microcystic aeruginosa (resting cells), were isolated from the sediment in the Uiam Dam in the North Han River and near Ugok Bridge in the Nakdong River, respectively. The morphology, germination process and rates, and growth was evaluated in different environmental conditions. D. cercinalis germination began on day two of culturing, with maximum cell growth observed on day ten. In contrast, M. aeruginosa exhibited daily increase in cell density and colony size, with notable density increase on day six. Next, different environmental conditions were assessed. Akinetes exhibited high germination rates at low light intensity (5—30 µmol/m2/s), whereas resting cells exhibited high growth rates at high light intensity (50—100 µmol/m2/s). Furthermore, both cell types exhibited optimum germination and growth in media containing N and P at 20—30° at a pH of 7—9. Our study reveals the optimum conditions for the germination and growth of cyanobacterial akinetes and resting cells isolated from river sediment, respectively, and will assist in predicting cyanobacterial blooms for appropriate management.

Photoinhibition and β-carotene production from Dunaliella sp. isolated from salt pans of Goa

The microalgae Dunaliella is a commercially viable species and is well known for its extreme environmental tolerance and β-carotene production under stressful conditions. We examined the effect of salinity and light intensity on the growth and β-carotene production, respectively, in two different species of Dunaliella: Dunaliella sp. and D. salina, isolated from the salt pans of Goa. Both the species were cultured in growth media with different salinity levels to establish the optimum salinity favouring maximum cell growth. Thereafter, the cells were cultured under optimum NaCl concentration, exposed to a range of light intensity and monitored for β-carotene production. The two species, identified based on their molecular characteristics, displayed a significant difference in growth and β-carotene production. Both D. salina and Dunaliella sp. achieved a maximum of 11.82 × 106 cells mL−1 (0.613 µd−1) and 18.76 × 106 cells mL−1 (0.731 µd−1) at 0.75 M and 0.5 M salinity, respectively. D. salina accumulated a large amount of total carotenoid (36.95 pg. cell−1) when cultured at 0.75 M salinity and exposed to high light intensity (1000 µmol m−2 S−1). In contrast, the carotenoid content per cell was low in Dunaliella sp. (3.07 pg. cell−1) when cultured under optimal salinity (0.5 M) and high light intensity, indicating photoinhibition. We found that different Dunaliella species exhibit different photo-physiological properties that need further evaluation to identify the right candidate for industrial applications.

Super enhancement of methanethiol biodegradation by new isolated Pseudomonas sp. coupling silicone particles

A new strain, Pseudomonas sp. SJ-1, which was able to remove model odorous organics methanethiol (MT) has been isolated from the wastewater treatment plant and identified via 16S rRNA analysis. Initial MT concentration, temperature and pH played an important role in MT removal, and up to 100% of 260 mg L−1 of MT could be removed within 11 h under the optimum conditions (30 °C, pH 7.0) with an average degradation rate of 23.6 mg L−1 h−1, which was the highest one in literature so far. The silicone particles were added as the non-aqueous phases (NAP) to enhance the performance of MT degradation. The results indicated that the maximum degradation rate and specific cell growth of strain SJ-1 were 2.36 times and 1.31 times by Haldane kinetic model analysis in the NAP added test. The SO42− was identified as the major intermediate and CO2 as a final product in MT biodegradation. Overall, this is the first report that a newly isolated Pseudomonas sp. could use high concentration MT as sole energy source and carbon source and its activity could be enhanced by adding NAP. The results provide a suggestion for the development of more effective and reliable biological treatment processes.

Developing Microbial Co-Culture System for Enhanced Polyhydroxyalkanoates (PHA) Production Using Acid Pretreated Lignocellulosic Biomass.

In the growing polymer industry, the interest of researchers is captivated by bioplastics production with biodegradable and biocompatible properties. This study examines the polyhydroxyalkanoates (PHA) production performance of individual Lysinibacillus sp. RGS and Ralstonia eutropha ATCC 17699 and their co-culture by utilizing sugarcane bagasse (SCB) hydrolysates. Initially, acidic (H2SO4) and acidified sodium chlorite pretreatment was employed for the hydrolysis of SCB. The effects of chemical pretreatment on the SCB biomass assembly and its chemical constituents were studied by employing numerous analytical methods. Acidic pretreatment under optimal conditions showed effective delignification (60%) of the SCB biomass, leading to a maximum hydrolysis yield of 74.9 ± 1.65% and a saccharification yield of 569.0 ± 5.65 mg/g of SCB after enzymatic hydrolysis. The resulting SCB enzymatic hydrolysates were harnessed for PHA synthesis using individual microbial culture and their defined co-culture. Co-culture strategy was found to be effective in sugar assimilation, bacterial growth, and PHA production kinetic parameters relative to the individual strains. Furthermore, the effects of increasing acid pretreated SCB hydrolysates (20, 30, and 40 g/L) on cell density and PHA synthesis were studied. The effects of different cost-effective nutrient supplements and volatile fatty acids (VFAs) with acid pretreated SCB hydrolysates on cell growth and PHA production were studied. By employing optimal conditions and supplementation of corn steep liquor (CSL) and spent coffee waste extracted oil (SCGO), the co-culture produced maximum cell growth (DCW: 11.68 and 11.0 g/L), PHA accumulation (76% and 76%), and PHA titer (8.87 and 8.36 g/L), respectively. The findings collectively suggest that the development of a microbial co-culture strategy is a promising route for the efficient production of high-value bioplastics using different agricultural waste biomass.

Cytotoxic and Antioxidant Effects of Phoenix dactylifera L. (Ajwa Date Extract) on Oral Squamous Cell Carcinoma Cell Line.

Aim The aim of the current study is to investigate the antioxidant and apoptotic potential of Ajwa date flesh (ADF) and Ajwa date pit (ADP) extract on human squamous cell carcinoma cell line (HSC-2). Method ADF and ADP were extracted with a solvent extraction method using hexane, acetone, and ethanol, which were then subjected to antioxidant assay by 2,2-diphenyl-1-picrylhydrazyl (DPPH). HSC-2 cells were then treated with different concentrations of ADF and ADP extract for 24, 48, and 72 hours. MTT assay was performed to assess the antiproliferative effect, and Annexin V-FITC was used for the detection of cellular apoptosis. Results Acetone extracts of ADF and ADP had the highest radical scavenging and antioxidant activities followed by the ethanolic extracts, whereas ADP appeared to have significantly higher antioxidant effects than ADF. MTT assay demonstrated that acetone extracts of ADF and ADP were significantly cytotoxic against HSC-2 cells in a dose- and time-dependent manner. The half inhibitory concentration (IC50) of ADF was found to be 8.69 mg/ml at 24 h, and the maximum cell growth inhibition was observed at 50 mg/ml. The IC50 for the ADP was found to be 0.97 mg/ml at 24 h, and the maximum cell growth inhibition was observed at 5 mg/ml. Statistical analysis of the flow cytometry assay showed that the treatment with ADF and ADP extracts had a significant apoptotic effect which occurred in a dose-dependent manner. HSC-2 cells were seen in the late apoptotic stage with higher doses of ADF and ADP extract. ADP extract demonstrated higher apoptotic activity than ADF extract. In addition, combined treatment of ADF and ADP was also performed on HSC-2 cells which demonstrated higher apoptotic activity when compared to the single extract. Conclusion Ajwa date fruit has a promising cytotoxic effect by inhibiting the growth and proliferation of OSCC cells and inducing cell death by apoptosis.

The benthic toxic dinoflagellate Ostreopsis cf. ovata in the NW Mediterranean Sea: Relationship between sea surface temperature and bloom phenology

Blooms of the toxic benthic dinoflagellate Ostreopsis cf. ovata can induce ecological and human health issues in certain temperate areas. In order to prevent these negative effects, long-term monitoring studies of O. cf. ovata blooms have been conducted in several impacted areas to have a comprehensive understanding of bloom dynamics and efficient tools for risk management.O. cf. ovata blooms were monitored every summer (from mid-June to the end of August) on five identified sites in Larvotto beach (Monaco, NW Mediterranean Sea), between 2007 and 2019. This time-series represents one of the largest time-series in the world describing blooms of this species.Bloom phenological features (timing, duration, maximum cell abundance and growth rate), were found to be highly variable throughout the studied period, and were analyzed as a function of different hydroclimatic parameters, including sea surface temperature (SST). The highest net growth rates were related to temperatures ranging between 21°C and 25°C, and did not coincide with maximal temperature records (27.5°C). Such results suggest that, although global warming possibly influences the expansion of O. cf. ovata from tropical to temperate waters, the definite impact of temperature on bloom dynamics might be more complex than a simple facilitation factor for algal growth, at least in NW Mediterranean waters.Furthermore, monthly SST anomalies calculated over this 13-year survey showed a strong positive correlation between spring SST positive anomalies and the bloom starting date, indicating that blooms occurred earlier in the season when spring SSTs were warmer than usual.Overall results provide tools to modelers and managers who are facing crucial challenges to predict the distribution and phenology of O. cf. ovata blooms in European coastal waters, moreover in a context of global warming.

Enhanced production and characterization of coenzyme Q10 from Rhodobacter sphaeroides using a potential fermentation strategy

BackgroundThe demand for Coenzyme Q10 (CoQ10) to the human body is increasing due to its potential health function. However, the production of CoQ10 in yields remains a big problem for commercialization. MethodsThis study attempts to develop a useful fermentation strategy for enhancing the production of CoQ10 from the Rhodobacter sphaeroides. Significant FindingsIt was observed that the cell growth, the concentration and the content of CoQ10 were further enhanced to 11.44 g/L, 60.02 mg/L and 5.25 mg/g by the assimilation of 2 g/L of vitamin B1. This fed-batch culture using vitamin B1 as a feeding substrate resulted into the cell growth, the CoQ10 production and the CoQ10 content of 16.5 g/L, 88.7 mg/L and 5.38 mg/g respectively. Moreover, the fed-batch culture with 100% medium replacement of 12 h-, 24 h- and 48 h-cultivations were also performed. The maximal cell growth, CoQ10 production and CoQ10 content were found to be 37.65 g/L, 138.24 mg/L and 3.67 mg/g, respectively. Eventually, this study also identified the CoQ10 produced by R. sphaeroides using FAB-MS and 1HNMR . It was suggested that by optimizing the environmental factors, the CoQ10 production was enhanced by 3.42 folds for fed-batch culture when compared with the batch cultivation.

Cold plasma promotes Sertoli cell proliferation via AMPK–mTOR signaling pathway

This study investigated cold plasmas for multiple biological applications. Our previous work has found dielectric barrier discharge plasma improves chicken sperm quality. The number of Sertoli cells (SCs) decides spermatogenesis. However, whether cold plasma can regulate SC proliferation remains unclear. This study explored the effects of cold plasma on immature chicken SC proliferation and the regulation mechanism. Results showed that cold plasma exposure at 2.4 W for 30 s twice with an interval of 6 h produced (P<0.05) the maximum SC viability, cell growth, and cell cycle progression. SC proliferation-promoting effect of cold plasma treatment was regulated by increasing (P<0.05) the adenosine triphosphate production and the respiratory enzyme activity in the mitochondria. This process was potentially mediated by the adenosine monophosphate-activated protein kinase (AMPK)–mammalian target of rapamycin (mTOR) signaling pathway, which was regulated by the microRNA (miRNA) targeting regulation directly and by the intracellular reactive oxygen species homeostasis indirectly. The cold plasma treatment increased (P<0.01) the miR-7450-5p expression and led to a decreased (P<0.01) AMPKα1 level. On the other hand, miR-100-5p expression was reduced (P<0.05) and led to an increased (P<0.05) mTOR level in SCs. A single-stranded synthetic miR-7450-5p antagomir and a double-stranded synthetic miR-100-5p agomir reduced (P<0.05) the SC proliferation. However, this could be ameliorated (P<0.05) by the cold plasma treatment. Our findings suggest that appropriate cold plasma treatment provides a safe strategy to improve SC proliferation, which is beneficial to elevating male chicken reproductive capacity.

Biological Evaluation of Cissus vitiginea Leaves Ethanol Extract with Anticancer Activities against MCF-7 and Vero Cell Lines

The present study investigated the phytoconstituents and anticancer potential followed by apoptotic studies of Cissus vitiginea leaves ethanol extracts on MCF-7 and Vero cells. Qualitative phytochemical analysis revealed the presence of carbohydrate, saponins, flavonoids, alkaloids, anthocyanin and betacyanin, quinones, glycosides, cardiac glycosides, terpenoids, triterpenoids, phenols, coumarins, acids, protein and steroids. On the other hand, tannins were absent in the ethanol extract. A dose-dependent anti-proliferative assay revealed that the 50% cell viability was observed at the concentration of 125 μg/ml with the ethanol extract. The maximum cell growth inhibition was observed at the concentration 1000 μg/ml (24.64 %). From the obtained data the ethanol extract were able to reduce the viability of MCF-7 cell line in direct dose dependent manner and thereafter, ethanol leaf extract was taken for further studies to assess it biocompatibility with Vero cells. Treatment of Vero cells with 24 h at different concentration of ethanol extract did not cause any changes in the Vero cells. From the results, it is clear that ethanol extract is biocompatible and can be used as a drug for treating various diseases including cancer

Growth and nitrogen uptake by Arthrospira platensis cultured in aquaculture wastewater from Nile tilapia reared in biofloc system

This study aimed to evaluate the growth of Arthrospira (Spirulina) platensis cultivated in Zarrouk culture medium and effluent from Nile tilapia (Oreochromis niloticus) reared in biofloc system. Four treatments were used: Control (100% Zarrouk), E50 (50% Zarrouk + 50% Tilapia effluent), E75 (25% Zarrouk + 75% Tilapia effluent), and E100 (100% Tilapia effluent), and the experiment lasted 10 days. Growth parameters such as maximum cell density (MCD), doubling time (DT), and growth rate (K) were daily evaluated, as well as pH and water temperature. In addition, the concentrations of total ammonia nitrogen (TAN), nitrite-N (NO2-N), and nitrate-N (NO3-N) were analyzed in order to compare nitrogen absorption. Among treatments, E50 and E75 obtained higher maximum cell densities and presented an exponential growth rate similar to the control treatment. Regarding the concentrations of nitrogen compounds, a significant reduction was observed in all treatments, with an NO3-N uptake of 99%, followed by 80% of TAN and 90% of NO2-N. Thus, giving the results obtained, besides being able to grow in wastewater, A. platensis can also be used in bioremediation processes, confirming the potential of this species.

Characterization of the Psychrotrophic Lactic Acid Bacterium Leuconostoc gelidum subsp. aenigmaticum LS4 Isolated from Kimchi Based on Comparative Analyses of Its Genomic and Phenotypic Properties.

With the aim of developing a new food starter culture, twenty-three psychrotrophic lactic acid bacteria (LAB) were isolated from 16 kimchi samples. One strain, Leuconostoc gelidum subsp. aenigmaticum LS4, which had typical psychrotrophic characteristics, was selected, and its phenotypic and genomic properties as a starter culture were investigated. The complete genome of L. aenigmaticum LS4 consisted of one circular chromosome (1,988,425 bp) and two plasmids (19,308 bp and 11,283 bp), with a guanine–cytosine content of 36.8%. L. aenigmaticum LS4 could grow at 5 °C but not at 37 °C, and maximum cell growth was obtained at 15~25 °C. L. aenigmaticum LS4 did not show any harmful characteristics such as hemolysis, undesirable enzyme activities, biogenic amine production, or antibiotic resistance. L. aenigmaticum LS4 was investigated for its suitability for technological processes (pH, temperature and NaCl treatment). L. aenigmaticum LS4 exhibited strong antimicrobial activity caused by the production of organic acids and bacteriocin, and it produced an exopolysaccharide composed of glucose with a molecular weight of 3.7 × 106 Da. Furthermore, L. aenigmaticum LS4 improved the organoleptic qualities of kimchi juice. Our results indicate that L. aenigmaticum LS4 could be used as a functional starter culture for food (vegetable or fruit) fermentation at low temperatures.