67 research outputs found
Bio surfactant production in sugar beet molasses by some Pseudomonas spp.
Abstract: In this study, rhamnolipid biosurfactant production was investigated in eighteen strains of Pseudomonas spp.. Rhamnolipid by these strains was determined by a spectrophotometric method in nutrient broth medium (NB). From the 18 strains screened, two Pseudomonas strains (Pseudomonas luteola B17 and Pseudomonas putida B12) which had produced the highest percentage yield of rhamnolipid were examined for rhamnolipid production at different incubation times (24, 48 and 72 hr) and different sugar beet molasses concentrations [1-5 % w/v concentration (1-5 g molasses/100 ml water)]. The rhamnolipid production increased with the increase in the concentration of molasses and maximum production occurred when 5 % (w/v) of molasses were used. At the same time, maximum rhamnolipid production occurred after 72 hr of incubation. When the amount of rhamnolipid produced at different incubation times (24, 48 and 72 hr) and with different concentrations of molasses [1-5 % w/v concentration (1-5 g molasses/100 ml water)] by Pseudomonas spp.; was compared, no significant difference in amount of production was seen. These studies show that the waste product from sugar industry may be suggested for important biotechnological processes such as rhamnolipid production
COMPARATIVE EVALUATION OF TOTAL PHENOLIC/CAROTENOID CONTENTS, CHLOROGENIC ACID/RUTIN PROFILES, AND ANTIOXIDANT PROPERTIES OF TWO PRANGOS SPECIES (P. UECHTRITZII AND P. PABULARIA)
Objective: The aim of the study was to investigate the antioxidant activities, chlorogenic acid/rutin profiles, and bioactive compounds' contents of the various extracts from Prangos uechtritzii Boiss. & Hausskn. and Prangos pabularia Lindl.Methods: The antioxidant capacities of the extracts were evaluated by various methods, including the plasma lipid peroxidation inhibitory, β-carotene/linoleic acid bleaching, free radical scavenging activity, and metal chelating activity assays. Chlorogenic acid and rutin contents of the extracts were determined qualitatively and quantitatively by high-performance liquid chromatography (HPLC). Total phenolic, β-carotene, and lycopene contents of the extracts were also determined.Results: In the assays, the methanol and the water extracts showed higher antioxidant activities than the acetone and ethyl acetate extracts. According to HPLC analysis, the richest extracts in terms of rutin and chlorogenic acid were determined as P. pabularia methanol extract (12.61±0.11 µg/mg) and P. uechtritzii methanol extract (4.76±0.12 µg/mg), respectively.Conclusion: It could be suggested that these Prangos species, especially the water extract of P. uechtritzii may be used a potential source of natural antioxidants for food and pharmacy industries.Â
Effects of some organic pollutants on the exopolysaccharides (EPSs) produced by some Pseudomonas spp. strains
In this study, isolation and characterization of exopolysaccharides produced by Pseudomonas aeruginosa B1, P fluorescens B5, P. stutzeri B11 and P. putida B15 which had been seen to produce exopolymers of potential interest in biotechnological applications were examined. To initiate the observation of the organic pollutants-polymer interactions, the yield and properties of their extracellular polysaccharide were researched. The exopolysaccharide production by these strains during growth in nutrient broth medium (control) was 41-75 mg L-1. Also, P aeruginosa B1, P fluorescens 135, P. stutzeri B11 and P putida B15 had exhibited high production of EPSs in presence of various organic pollutants (2,4-D, benzene, BTX and gasoline, respectively) in mineral salt medium (MSM) as a sole carbon source. EPS production by the 4 strains ranged from 40 mg L-1 to 8 mg L-1. Monosaccharide composition of EPS produced by these cultures were analyzed by HPLC. Results indicated that EPSs of strains contained neutral sugars and acetylated amino sugars. The neutral sugars in the EPS were mainly composed of glucose, arabinose, glycerol, ribose. The presence of galactronic acid, N-acetyl-D-galactosamin and N-acetyl-D-glucosamine indicated the acidic nature of the polysaccharide. Glycerol was the basic structural unit of EPS produced by the strains except P. stutzeri B11 (MSM with 1% BTX). Strain B11 (in NB medium) was found to be composed of neutral sugars (100%) while strain B1 [in MSM medium with 0.2% (v/v) 2.4-D] contained neutral sugars (70.0%), acetylated amino sugars (30.0%). Also, EPS content of strain B5 (in the NB medium) was neutral sugars (99.8%), acetylated amino sugars (0.2%) while the strain B5 [in MSM medium containing the 1% (v/v) benzene] was found to contain neutral sugars (99.9%), acetylated amino sugars (0.1%). However, EPS monomer composition by strain B11 was detected as neutral sugars (99.77%), acetylated amino sugars (0.23%) in NB medium while the strain B11 [in MSM medium with 1% (v/v) BTX] contained neutral sugars (98.2%) and acetylated amino sugars (1.8%). Lastly, in NB medium by strain B15 was found to contain neutral sugars (99.9%) and acetylated amino sugars (0.1%) while in MSM medium in the presence of 1% (v/v) gasoline it was found to contain neutral sugars (83.6%), acetylated amino sugars (16.4%). Monomer composition of control EPSs changed to different structures in the presence of various organic pollutants. Diversities of organic compounds as carbon source affected the monomer composition of EPS produced by some Pseudomonas spp. cultures. (C) 2009 Elsevier B.V. All rights reserved
Antiproliferative, neurotoxic, genotoxic and mutagenic effects of toxic cyanobacterial extracts
Cyanobacteria are the rich resource of various secondary metabolites including toxins with broad pharmaceutical significance. The aim of this work was to evaluate the antiproliferative, neurotoxic, genotoxic and mutagenic effects of cyanobacterial extracts contain-ing Microcystin-LR (MCLR) in vitro. ELISA analysis results showed that MCLR contents of five cyanobacterial extracts were 2.07 ng/mL, 1.43 ng/mL, 1.41 ng/mL, 1.27 ng/mL, and 1.12 ng/mL for Leptolyngbya sp. SB1, Phormidium sp. SB4, Oscillatoria earlei SB5, Phormidium sp. SB2, Uncultured cyanobacterium, respectively. Phormidium sp. SB4 and Phormidium sp. SB2 extracts had the lowest neurotoxicity (86% and 79% cell viability, respectively) and Oscillatoria earlei SB5 extracts had the highest neurotoxicity (47% cell viability) on PC12 cell at 1000 μg/ml extract concentration. Leptolyngbya sp. SB1 and Phormidium sp. SB2 showed the highest antiproliferative effect (92% and 77% cell death) on HT29 cell. On the other hand, all concentrations of five toxic cyanobacterial extracts induced DNA damage between 3.0% and 1.3% of tail intensity and did not cause any direct mutagenic effect at the 1000 μg/plate cyanobacterial extracts. These results suggest that cyanobacteria-derived MCLR is a promising candidate for development of effective agents against colon cancer.University of Nevsehir Hacı Bektas Veli, Scientific Research Projects Unit (Project no: NEUBAP13F43
Gut-lung axis and dysbiosis in COVID-19
COVID-19, a novel infectious disease, caused by SARS-CoV-2, affected
millions of people around the world with a high mortality rate. Although
SARS-CoV-2 mainly causes lung infection, gastrointestinal symptoms
described in COVID-19 patients and detection of the viral RNA in feces
of infected patients drove attentions to a possible fecal-oral
transmission route of SARS-CoV-2. However, not only the viral RNA but
also the infectious viral particles are required for the viral infection
and no proof has been demonstrated the transmission of the infectious
virus particles via the fecal-oral route yet. Growing evidence indicates
the crosstalk between gut microbiota and lung, that maintains host
homeostasis and disease development with the association of immune
system. This gut-lung interaction may influence the COVID-19 severity in
patients with extrapulmonary conditions. Severity of COVID-19 has mostly
associated with old ages and underlying medical conditions. Since the
diversity in the gut microbiota decreases during aging, dysbiosis could
be the reason for older adults being at high risk for severe illness
from COVID-19. We believe that gut microbiota contributes to the course
of COVID-19 due to its bidirectional relationship with immune system and
lung. Dysbiosis in gut microbiota results in gut permeability leading to
secondary infection and multiple organ failure. Conversely, disruption
of the gut barrier integrity due to dysbiosis may lead to translocation
of SARS-CoV-2 from the lung into the intestinal lumen via circulatory
and lymphatic system. This review points out the role of dysbiosis of
the gut microbiota involving in sepsis, on the severity of SARS-CoV-2
infection. Additionally, this review aims to clarify the ambiguity in
fecal-oral transmission of SARS- CoV-2
Characterization of lactic acid bacteria derived exopolysaccharides for use as a defined neuroprotective agent against amyloid beta(1-42)-induced apoptosis in SH-SY5Y cells
Alzheimer's disease (AD) is a disease characterized by cerebral neuronal
degeneration and loss in a progressive manner. Amyloid beta (A beta) in
the brain is toxic to neurons, being a main risk factor for initiation
and continuation of cognitive deterioration in AD. Neurotoxicity of A
beta origin is also linked to oxidative stress characterized by
excessive lipid peroxidation, protein oxidation, changes in antioxidant
systems, and cerebral DNA damage in AD. Furthermore, A beta can induce
oxidative neuronal cell death by a mitochondrial dysfunction. Cellular
injury caused by oxidative stress can be possibly prevented by boosting
or promoting bodily oxidative defense system by supplying antioxidants
in diet or as medications. However, most synthetic antioxidants are
found to have cytotoxicity, which prevents their safe use, and limits
their administration. For this reason, more attention has been paid to
the natural non-toxic antioxidants. One of the most promising groups of
non-toxic antioxidative compounds is thought to be polysaccharides. This
study investigated the characterization and protective action exerted by
exopolysaccharides (EPSs) originated from Lactobacillus delbrueckii ssp.
bulgaricus B3 and Lactobacillus plantarum GD2 to protect from apoptotic
activity exerted by A beta (1-42) among SH-SY5Y cells. We characterized
EPSs by elemental analysis, FTIR, AFM, SEM, and XRD. The antioxidant
effects of EPSs were determined by the DPPH free radical scavenging
activity, hydroxyl radical scavenging activity, metal ion chelating
activity, lipid peroxidation inhibitory activity, and superoxide anion
scavenging activity method. The protective effects of EPSs were
determined by flow cytometry and RT-PCR. Mannose ratio, molecular
weight, functional groups, surface morphology, and amorphous character
structure of EPSs are thought to play a role in the protective effect of
EPSs. EPSs reduced apoptotic activity of A beta (1-42) in addition to
their depolarizing effect on mitochondrial membrane potential in
concentration-dependent manner. These observations contribute the
inclusion of EPSs among the therapeutic options used to manage various
neurological disorders in the traditional medicine in a scientific
manner, indicating that EPSs may be promising natural chemical
constituents that need advanced research and development for
pharmacological therapy of AD
Influence of different carbon sources on exopolysaccharide production by Lactobacillus delbrueckii subsp. bulgaricus (B3, G12) and Streptococcus thermophilus (W22)
Exopolysaccharides (EPSs) production was studied by Lactobacillus delbrueckii subsp. bulgaricus (B3, G12) and Streptococcus thermophilus (W22) in the medium containing various carbon sources (glucose, fructose, sucrose or lactose). For all the strains, glucose was the most efficient carbon source and B3, G12 and W22 strains produced 211, 175 and 120 EPS mg/L respectively. Also, the influence of different concentrations of glucose (5,10,15,20,25,30 g/L) on EPS production and growth was studied. The results indicated that EPS production and growth were stimulated by the high glucose concentration (30 g/L)
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